Large

We are creative thinkers with decades of clinical trial experience who drive innovative solutions powered by insights from data and technology. As we tackle challenges in today’s world, we know that we need to be nimble and agile. That’s why we work side-by-side with our partners to eliminate inefficiencies from the process so we can help them deliver life-changing therapies faster for patients, caregivers and healthcare providers worldwide.

Science & Healthcare

Fortrea

Healthcare

You need independent monitoring experience, a focus on oncology, and exposure to diverse protocols. Expect 8+ on-site days/month across the UK using a remote-based, risk-based monitoring model.

You will conduct national monitoring for oncology studies, manage multiple protocols, utilize risk-based monitoring, and complete 8+ on-site days monthly across various therapeutic areas.

Research & Development

Reading

Our Clinical Operations team in the UK is looking for a passionate CRAI with previous independent monitoring experience to work across a diverse range of therapeutic areas - including Oncology. This is your chance to gain hands-on experience in groundbreaking clinical trials while being part of a supportive, fast-paced and innovative global CRO. What You Can Expect ✅ National monitoring across the UK (remote-based) ✅ Oncology focus, including solid tumor studies, Prostate, NSCLC, Leukemia, Breast, Glioblastoma & Hematological Malignancies ✅ Exposure to multiple protocols across Neuroscience, Cell/Gene Therapies, Respiratory, Cardiovascular, Infectious Disease, Nephrology, Endocrinology & Gastroenterology ✅ Risk-based monitoring model for smarter trial management ✅ 8+ on-site days per month At our global CRO, we blend 30 years of expertise with innovation, offering: 🌟 Personalized development plans & career progression 🌟 A supportive environment with flexible Line Managers 🌟 Exciting collaborations with biotech & biopharma pioneers Make a real impact in clinical research while building your career with a company that invests in your growth and success! Ready to make a difference? Let’s connect! Learn more about our EEO & Accommodations request here.

Our Clinical Operations team in the UK is looking for a passionate CRAI with previous independent monitoring experience to work across a diverse range of therapeutic areas - including Oncology. This is your chance to gain hands-on experience in groundbreaking clinical trials while being part of a supportive, fast-paced and innovative global CRO.What You Can Expect✅ National monitoring across the UK (remote-based)✅ Oncology focus, including solid tumor studies, Prostate, NSCLC, Leukemia, Breast, Glioblastoma & Hematological Malignancies✅ Exposure to multiple protocols across Neuroscience, Cell/Gene Therapies, Respiratory, Cardiovascular, Infectious Disease, Nephrology, Endocrinology & Gastroenterology✅ Risk-based monitoring model for smarter trial management✅ 8+ on-site days per monthAt our global CRO, we blend 30 years of expertise with innovation, offering:🌟 Personalized development plans & career progression🌟 A supportive environment with flexible Line Managers🌟 Exciting collaborations with biotech & biopharma pioneersMake a real impact in clinical research while building your career with a company that invests in your growth and success!Ready to make a difference? Let’s connect!Learn more about our EEO & Accommodations request here.

Clinical Research Associate I - Fortrea

Our &lt;strong&gt;Clinical Operations&lt;/strong&gt; team in the UK is looking for a passionate &lt;strong&gt;CRAI&lt;/strong&gt; with &lt;strong&gt;previous independent monitoring experience&lt;/strong&gt; to work across a diverse range of therapeutic areas - including &lt;strong&gt;Oncology&lt;/strong&gt;. This is your chance to gain hands-on experience in groundbreaking clinical trials while being part of a &lt;strong&gt;supportive, fast-paced and innovative&lt;/strong&gt; global CRO.&lt;br&gt;&lt;br&gt;&lt;strong&gt;What You Can Expect&lt;br&gt;&lt;br&gt;&lt;/strong&gt;✅ &lt;strong&gt;National monitoring across the UK&lt;/strong&gt; (remote-based)&lt;br&gt;&lt;br&gt;✅ &lt;strong&gt;Oncology focus&lt;/strong&gt;, including solid tumor studies, Prostate, NSCLC, Leukemia, Breast, Glioblastoma &amp;amp; Hematological Malignancies&lt;br&gt;&lt;br&gt;✅ &lt;strong&gt;Exposure to multiple protocols&lt;/strong&gt; across Neuroscience, Cell/Gene Therapies, Respiratory, Cardiovascular, Infectious Disease, Nephrology, Endocrinology &amp;amp; Gastroenterology&lt;br&gt;&lt;br&gt;✅ &lt;strong&gt;Risk-based monitoring model&lt;/strong&gt; for smarter trial management&lt;br&gt;&lt;br&gt;✅ &lt;strong&gt;8+ on-site days per month&lt;br&gt;&lt;br&gt;&lt;/strong&gt;At our &lt;strong&gt;global CRO&lt;/strong&gt;, we blend 30 years of expertise with innovation, offering:&lt;br&gt;&lt;br&gt;🌟 &lt;strong&gt;Personalized development plans &amp;amp; career progression&lt;br&gt;&lt;br&gt;&lt;/strong&gt;🌟 &lt;strong&gt;A supportive environment with flexible Line Managers&lt;br&gt;&lt;br&gt;&lt;/strong&gt;🌟 &lt;strong&gt;Exciting collaborations with biotech &amp;amp; biopharma pioneers&lt;br&gt;&lt;br&gt;&lt;/strong&gt;Make a real impact in clinical research while building your career with a company that invests in &lt;strong&gt;your growth and success&lt;/strong&gt;!&lt;br&gt;&lt;br&gt;&lt;strong&gt;Ready to make a difference? Let’s connect!&lt;br&gt;&lt;br&gt;&lt;/strong&gt;Learn more about our EEO &amp;amp; Accommodations request here.

Clinical Research Associate I

United Kingdom

You must have a relevant degree or equivalent experience, monitoring experience in clinical trials, knowledge of ICH/GCP, strong organization and communication skills, and fluent German and good English.

You will manage site selection, oversee study centers, train and mentor new staff, and contribute as a Subject Matter Expert in specialized internal projects.

<div>As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in ~100 countries, Fortrea is transforming drug and device development for partners and patients across the globe. 
 
Als f&uuml;hrendes globales Auftragsforschungsinstitut (CRO) mit einer Leidenschaft f&uuml;r wissenschaftliche Pr&auml;zision und einer jahrzehntelangen Erfahrung in der klinischen Entwicklung, bietet Fortrea Kunden aus der Pharma-, Biotechnologie- und Medizintechnikbranche ein breites Spektrum an L&ouml;sungen f&uuml;r die klinische Entwicklung, den Patientenzugang und die Technologie in mehr als 20 Therapiebereichen. Mit &uuml;ber 19.000 Mitarbeitern, in mehr als 90 L&auml;ndern, ver&auml;ndert Fortrea die Arzneimittel- und Medizinprodukteentwicklung f&uuml;r Partner und Patienten auf der ganzen Welt. 
 
Diese Vakanz ist f&uuml;r kommende Personalressourcen gedacht, die wir voraussichtlich ben&ouml;tigen werden.
 
 
Als CRA in unserer Abteilung Flexible Solutions sind Sie von zentraler Bedeutung f&uuml;r die erfolgreiche Durchf&uuml;hrung komplexer klinischer Studien (Phasen I - III) in Deutschland.
 
 
Sie wirken an der Entwicklung innovativer Medikamente, die einen neuen Standard insbesondere im Bereich der Onkologie setzen, mit, w&auml;hrend Sie exklusiv f&uuml;r einen unserer wichtigsten internationalen Kunden t&auml;tig sind. 
 
Wenn Sie Ihr therapeutisches Fachwissen erweitern und gleichzeitig Ihre Karriere in einem erstklassigen pharmazeutischen Arbeitsumfeld weiter voranbringen m&ouml;chten, ist dies eine hervorragende Gelegenheit. Kommen Sie zu uns und &uuml;berzeugen Sie sich selbst, warum mehr als 90 % der 20 weltweit f&uuml;hrenden Pharmaunternehmen seit vielen Jahren zu unseren Kunden z&auml;hlen! 
 
Was Sie von uns erwarten d&uuml;rfen: 
<ul><li>
eine bedeutungsvolle T&auml;tigkeit in einem stabilen, diversen, erfolgreichen und angesehenen Unternehmen</li><li>
eine attraktive und konkurrenzf&auml;hige Verg&uuml;tung, einschlie&szlig;lich 13. Gehalt und Urlaubsgeld</li><li>
eine echte Work-Life-Balance</li><li>
flexible Arbeitszeiten sowie betriebliche Regelungen zum Freizeitausgleich</li><li>
Reisezeit = Arbeitszeit</li><li>
ein umfassendes Onboarding mit Unterst&uuml;tzung durch Ihren pers&ouml;nlichen Mentor</li><li>
einen unbefristeten Home-Office-Arbeitsvertrag</li><li>
einen attraktiven, arbeitgeberfinanzierten Pensionsplan</li><li>
hervorragende Fortbildungs- und Entwicklungsm&ouml;glichkeiten innerhalb Fortreas sowie Unterst&uuml;tzung bei Ihren pers&ouml;nlichen Weiterbildungspl&auml;nen</li><li>
kontinuierliche Unterst&uuml;tzung durch Ihren Line Manager, Ihr Team sowie &uuml;ber 19&lsquo;000 Kolleg*innen weltweit</li></ul> 

Ihre Aufgaben: 
<ul><li>
alle Aspekte des Site Managements, von der Auswahl der Studienzentren bis hin zum Close-Out</li><li>
Unterst&uuml;tzung bei Training, Mentoring und Weiterentwicklung neuer Mitarbeiter, z. B. bei Co-Monitoring-Besuchen in den Studienzentren</li><li>
Mitarbeit in kundenspezifischen Arbeitsgruppen und anderen internen Projekten als Subject Matter Expert</li></ul> 

Ihr Background: 
<ul><li>
Hochschulabschluss in einem relevanten Fachbereich wie z.B. Biologie, Biochemie, Chemie, Gesundheitsmanagement, Pharmakologie, (Veterin&auml;r-) Medizin usw.</li><li>
alternativ eine abgeschlossene Berufsausbildung im Bereich Gesundheit / Pflege, oder gleichwertige Berufserfahrung in der klinischen Forschung (z. B. als Study Nurse, Research Nurse, Studienkoordinator*in...)</li><li>
Berufserfahrung im unabh&auml;ngigen Monitoring von klinischen Studien in Deutschland, gesammelt bei einer CRO oder einem pharmazeutischen Unternehmen</li><li>
gute Kenntnis der geltenden deutschen und internationalen Regularien bei klinischen Studien wie z.B. ICH / GCP</li><li>
ein gutes Organisationstalent, Empathie, sowie eine sorgf&auml;ltige und detailgenaue Arbeitsweise</li><li>
ausgezeichnete Kommunikationsf&auml;higkeiten in verhandlungssicherem Deutsch sowie gute Englischkenntnisse in Wort und Schrift sind ein Muss</li></ul> 
Fortrea sucht aktiv nach motivierten, l&ouml;sungsorientierten und kreativen Denkern, die unsere Leidenschaft f&uuml;r die &Uuml;berwindung von Hindernissen bei klinischen Studien teilen. Unser Ziel ist es, den Entwicklungsprozess zu revolutionieren und sicherzustellen, dass lebensver&auml;ndernde Ideen und Therapien schnellstm&ouml;glich Patienten zur Verf&uuml;gung gestellt werden. Werden Sie Teil unseres au&szlig;ergew&ouml;hnlichen Teams und profitieren Sie von einem kollaborativen Arbeitsumfeld, in dem Ihre pers&ouml;nliche Entwicklung gef&ouml;rdert wird und Sie einen bedeutenden globalen Einfluss aus&uuml;ben k&ouml;nnen. Weitere Informationen &uuml;ber Fortrea finden Sie unter www.fortrea.com. 
 
#LI-GQ1 #LI-Remote
 
 
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com. 
 
Fortrea is proud to be an Equal Opportunity Employer: 
 
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply. 
 
For more information about how we collect and store your personal data, please see our Privacy Statement.
 
 
If, as a result of a disability, you require a reasonable accommodation to complete your job application, pre-employment testing, job interview or to otherwise participate in the hiring process, please contact: taaccommodationsrequest@fortrea.com. Please note that this e-mail address is only for job seekers requesting an accommodation. Please do not use this e-mail to check the status of your application.</div>

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in ~100 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

Als führendes globales Auftragsforschungsinstitut (CRO) mit einer Leidenschaft für wissenschaftliche Präzision und einer jahrzehntelangen Erfahrung in der klinischen Entwicklung, bietet Fortrea Kunden aus der Pharma-, Biotechnologie- und Medizintechnikbranche ein breites Spektrum an Lösungen für die klinische Entwicklung, den Patientenzugang und die Technologie in mehr als 20 Therapiebereichen. Mit über 19.000 Mitarbeitern, in mehr als 90 Ländern, verändert Fortrea die Arzneimittel- und Medizinprodukteentwicklung für Partner und Patienten auf der ganzen Welt.

Diese Vakanz ist für kommende Personalressourcen gedacht, die wir voraussichtlich benötigen werden.


Als CRA in unserer Abteilung Flexible Solutions sind Sie von zentraler Bedeutung für die erfolgreiche Durchführung komplexer klinischer Studien (Phasen I - III) in Deutschland.


Sie wirken an der Entwicklung innovativer Medikamente, die einen neuen Standard insbesondere im Bereich der Onkologie setzen, mit, während Sie exklusiv für einen unserer wichtigsten internationalen Kunden tätig sind.

Wenn Sie Ihr therapeutisches Fachwissen erweitern und gleichzeitig Ihre Karriere in einem erstklassigen pharmazeutischen Arbeitsumfeld weiter voranbringen möchten, ist dies eine hervorragende Gelegenheit. Kommen Sie zu uns und überzeugen Sie sich selbst, warum mehr als 90 % der 20 weltweit führenden Pharmaunternehmen seit vielen Jahren zu unseren Kunden zählen!

Was Sie von uns erwarten dürfen:

eine bedeutungsvolle Tätigkeit in einem stabilen, diversen, erfolgreichen und angesehenen Unternehmen
eine attraktive und konkurrenzfähige Vergütung, einschließlich 13. Gehalt und Urlaubsgeld
eine echte Work-Life-Balance
flexible Arbeitszeiten sowie betriebliche Regelungen zum Freizeitausgleich
Reisezeit = Arbeitszeit
ein umfassendes Onboarding mit Unterstützung durch Ihren persönlichen Mentor
einen unbefristeten Home-Office-Arbeitsvertrag
einen attraktiven, arbeitgeberfinanzierten Pensionsplan
hervorragende Fortbildungs- und Entwicklungsmöglichkeiten innerhalb Fortreas sowie Unterstützung bei Ihren persönlichen Weiterbildungsplänen
kontinuierliche Unterstützung durch Ihren Line Manager, Ihr Team sowie über 19‘000 Kolleg*innen weltweit

Ihre Aufgaben:

alle Aspekte des Site Managements, von der Auswahl der Studienzentren bis hin zum Close-Out
Unterstützung bei Training, Mentoring und Weiterentwicklung neuer Mitarbeiter, z. B. bei Co-Monitoring-Besuchen in den Studienzentren
Mitarbeit in kundenspezifischen Arbeitsgruppen und anderen internen Projekten als Subject Matter Expert

Ihr Background:

Hochschulabschluss in einem relevanten Fachbereich wie z.B. Biologie, Biochemie, Chemie, Gesundheitsmanagement, Pharmakologie, (Veterinär-) Medizin usw.
alternativ eine abgeschlossene Berufsausbildung im Bereich Gesundheit / Pflege, oder gleichwertige Berufserfahrung in der klinischen Forschung (z. B. als Study Nurse, Research Nurse, Studienkoordinator*in...)
Berufserfahrung im unabhängigen Monitoring von klinischen Studien in Deutschland, gesammelt bei einer CRO oder einem pharmazeutischen Unternehmen
gute Kenntnis der geltenden deutschen und internationalen Regularien bei klinischen Studien wie z.B. ICH / GCP
ein gutes Organisationstalent, Empathie, sowie eine sorgfältige und detailgenaue Arbeitsweise
ausgezeichnete Kommunikationsfähigkeiten in verhandlungssicherem Deutsch sowie gute Englischkenntnisse in Wort und Schrift sind ein Muss
Fortrea sucht aktiv nach motivierten, lösungsorientierten und kreativen Denkern, die unsere Leidenschaft für die Überwindung von Hindernissen bei klinischen Studien teilen. Unser Ziel ist es, den Entwicklungsprozess zu revolutionieren und sicherzustellen, dass lebensverändernde Ideen und Therapien schnellstmöglich Patienten zur Verfügung gestellt werden. Werden Sie Teil unseres außergewöhnlichen Teams und profitieren Sie von einem kollaborativen Arbeitsumfeld, in dem Ihre persönliche Entwicklung gefördert wird und Sie einen bedeutenden globalen Einfluss ausüben können. Weitere Informationen über Fortrea finden Sie unter www.fortrea.com.

#LI-GQ1 #LI-Remote


Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.

Fortrea is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

For more information about how we collect and store your personal data, please see our Privacy Statement.


If, as a result of a disability, you require a reasonable accommodation to complete your job application, pre-employment testing, job interview or to otherwise participate in the hiring process, please contact: taaccommodationsrequest@fortrea.com. Please note that this e-mail address is only for job seekers requesting an accommodation. Please do not use this e-mail to check the status of your application.

Clinical Research Associate (w/m/d), sponsor-dedicated (w/m/d) - Home Office, Deutschland - Fortrea

Germany

Clinical Research Associate (w/m/d), sponsor-dedicated (w/m/d) - Home Office, Deutschland

You should be pursuing a relevant degree or have equivalent experience, skilled in Premiere Pro and After Effects, tech-savvy, and organized, with a passion for video production and editing.

You will assist in video production and editing, enhance animation skills, collaborate with the marketing team, prioritize projects, and coordinate meetings with Product and Campaign Managers.

Marketing

Design

<div>As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in ~100 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
We are excited to offer a 1-year Internship within our Global Marketing team.
This internship offers a hands-on opportunity to develop skills in video production, editing, and animation while maintaining brand consistency. You'll work on a variety of content, including filmed videos, in-house productions, and branded visuals, using Adobe Premiere Pro and After Effects. Additionally, you'll gain experience in AI-driven tools like ChatGPT, Sora, and Midjourney to enhance video workflows.
Collaboration is key&mdash;you'll work with marketing and product teams to support video-driven campaigns and learn how to prioritize projects effectively. If you're passionate about video storytelling, animation, and creative media, this role will help you build real-world experience in a fast-paced, innovative environment.
Summary of Responsibilities:
Video Content Creation &amp; Workflow 
Gain hands-on experience in video production and editing while maintaining brand consistency. Learn how to refine layout standards to create a cohesive brand presence across all videos. 
Video Editing &amp; Asset Integration 
Develop your editing skills by working on a variety of content, including filmed videos, in-house productions, and branded visuals. Learn how to adjust assets, charts, and graphics to align with brand guidelines and video formats.
Video Editing &amp; Animation 
Enhance your animation skills by creating engaging, dynamic elements that support storytelling. Gain experience in using animation to elevate video content while maintaining brand consistency.
Team Collaboration &amp; Workflow Integration
Collaborate with the extended marketing team, helping to identify opportunities to support video-driven campaigns and strategies.<ul><li>
Work with the Product Manager, to learn how to prioritize video projects for development and editing.</li><li>
Gain experience in scheduling and coordinating meetings with Product and Campaign Managers.</li></ul>
Qualifications (Minimum Required):<ul><li>
Currently pursuing a degree in Film Production, Media and Communication, Digital Media Production, Animation and Visual Effects, or Creative Media and Technology. Fortrea may consider relevant and equivalent experience in lieu of educational requirements.</li><li>
Experience with video editing and production using Adobe Premiere Pro and After Effects.</li><li>
Good knowledge and passion to advance your skillset using video editing software, specifically Adobe Premiere and After Effects, including working with video layouts</li><li>
Comfortable with tech, and looking to advance your knowledge and ability with:</li><li>
Microsoft Excel, PowerPoint, Word, and Outlook</li><li>
ChatGPT, Sora, Midjourney (AI prompts and use)</li><li>
Marketing Tools</li><li>
Animation skills are an additional bonus.</li><li>
English as this will be the main working language; any other languages are a bonus.</li><li>
Good organizational skills, with the desire to learn how to manage multiple video projects, while producing quality video content.</li></ul>
Preferred Qualifications Include:<ul><li>
Interest in developing your understanding and skillset within Graphic Design, using industry standard packages such as Adobe Creative Cloud; Premiere, Illustrator, Photoshop, InDesign.</li><li>
Interest in exploring and learning how AI tools can aid video and image generation.</li></ul>
Work Environment:
<ul><li>Remote working but you may be required to travel on occasion.</li></ul>
#LI-REMOTE
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
Fortrea is proud to be an Equal Opportunity Employer: 
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement.
If, as a result of a disability, you require a reasonable accommodation to complete your job application, pre-employment testing, job interview or to otherwise participate in the hiring process, please contact: taaccommodationsrequest@fortrea.com. Please note that this e-mail address is only for job seekers requesting an accommodation. Please do not use this e-mail to check the status of your application.</div>

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in ~100 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
We are excited to offer a 1-year Internship within our Global Marketing team.
This internship offers a hands-on opportunity to develop skills in video production, editing, and animation while maintaining brand consistency. You'll work on a variety of content, including filmed videos, in-house productions, and branded visuals, using Adobe Premiere Pro and After Effects. Additionally, you'll gain experience in AI-driven tools like ChatGPT, Sora, and Midjourney to enhance video workflows.
Collaboration is key—you'll work with marketing and product teams to support video-driven campaigns and learn how to prioritize projects effectively. If you're passionate about video storytelling, animation, and creative media, this role will help you build real-world experience in a fast-paced, innovative environment.
Summary of Responsibilities:
Video Content Creation & Workflow
Gain hands-on experience in video production and editing while maintaining brand consistency. Learn how to refine layout standards to create a cohesive brand presence across all videos.
Video Editing & Asset Integration
Develop your editing skills by working on a variety of content, including filmed videos, in-house productions, and branded visuals. Learn how to adjust assets, charts, and graphics to align with brand guidelines and video formats.
Video Editing & Animation
Enhance your animation skills by creating engaging, dynamic elements that support storytelling. Gain experience in using animation to elevate video content while maintaining brand consistency.
Team Collaboration & Workflow Integration
Collaborate with the extended marketing team, helping to identify opportunities to support video-driven campaigns and strategies.
Work with the Product Manager, to learn how to prioritize video projects for development and editing.
Gain experience in scheduling and coordinating meetings with Product and Campaign Managers.
Qualifications (Minimum Required):
Currently pursuing a degree in Film Production, Media and Communication, Digital Media Production, Animation and Visual Effects, or Creative Media and Technology. Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
Experience with video editing and production using Adobe Premiere Pro and After Effects.
Good knowledge and passion to advance your skillset using video editing software, specifically Adobe Premiere and After Effects, including working with video layouts
Comfortable with tech, and looking to advance your knowledge and ability with:
Microsoft Excel, PowerPoint, Word, and Outlook
ChatGPT, Sora, Midjourney (AI prompts and use)
Marketing Tools
Animation skills are an additional bonus.
English as this will be the main working language; any other languages are a bonus.
Good organizational skills, with the desire to learn how to manage multiple video projects, while producing quality video content.
Preferred Qualifications Include:
Interest in developing your understanding and skillset within Graphic Design, using industry standard packages such as Adobe Creative Cloud; Premiere, Illustrator, Photoshop, InDesign.
Interest in exploring and learning how AI tools can aid video and image generation.
Work Environment:
Remote working but you may be required to travel on occasion.
#LI-REMOTE
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
Fortrea is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement.
If, as a result of a disability, you require a reasonable accommodation to complete your job application, pre-employment testing, job interview or to otherwise participate in the hiring process, please contact: taaccommodationsrequest@fortrea.com. Please note that this e-mail address is only for job seekers requesting an accommodation. Please do not use this e-mail to check the status of your application.

Video Production and Editing Intern - Fortrea

United Arab Emirates

Canada

United States

Portugal

Netherlands

Ireland

Philippines

Italy

Spain

India

France

South Africa

Australia

Switzerland

Video Production and Editing Intern

You must have a relevant STEM degree, be up-to-date with tech trends, learn quickly, focus on customer value, and effectively engage across departments.

You will enhance user experience, support application modernization, contribute to cloud initiatives, and ensure the sustainability of IT service operations.

Software Engineering

IT & Cybersecurity

Durham

<div>As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in ~100 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
Are you ready to launch your career in technology?
Our 12-week hybrid paid internship offers hands-on experience in our Global Technology Transformation Office, where you&rsquo;ll collaborate with IT Infrastructure &amp; Operations experts on impactful tech initiatives.
Gain exposure to emerging technologies such as cloud computing, AI, machine learning, cybersecurity, technical project management, and agile software development. Beyond technical skills, you&rsquo;ll benefit from career development workshops, executive mentorship, and team-building challenges to prepare for a successful future.
Internship Assignment Summary:
<ul><li>Modern workplace &ndash; user experience technology transformation</li><li>
Technical debt and application modernization transformation</li><li>
Cloud center of excellence formation</li><li>
IT Service operation center of excellence sustainability</li></ul>
Main Requirements:<ul><li>
Degree focused on Computer Science, Computer Engineering, Computer Information Systems, IT Security, Informatics, Information Science/Technology, Management Information Systems, Software Engineering, Security and Risk Analysis, or other relevant STEM majors with Software/IT experience</li><li>
Up to date with current industry standards, trending software, and information technology development tools</li><li>
Ability to learn quickly and successfully navigate in a fast-paced environment</li><li>
Proactively learns new tools and identifies opportunities for improvement and promotes their adoption</li><li>
Contributes to creative solutions and challenges the status quo</li><li>
Strong customer focus, ability to understand the value proposition for the customer, and commitment to deliver the best value proposition</li><li>
Able to engage positively across multiple departments to establish clarity, vision, and mutual trust to achieve business goals</li></ul>
Qualifications (Minimum Required):<ul><li>
Degree focused on Computer Science, Computer Engineering, Computer Information Systems, IT Security, Informatics, Information Science/Technology, Management Information Systems, Software Engineering, Security and Risk Analysis.</li><li>
Relevant STEM majors with Software/IT experience.</li></ul>
This program is designed for students in STEM + Healthcare disciplines, offering real-world assignments that are both challenging and valuable to our organization.
If you&rsquo;re eager to work on cutting-edge technology projects and make a difference in the industry, this is your opportunity!
#LI-MI1
#LI-Hybrid
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
Fortrea is proud to be an Equal Opportunity Employer: 
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement.
If, as a result of a disability, you require a reasonable accommodation to complete your job application, pre-employment testing, job interview or to otherwise participate in the hiring process, please contact: taaccommodationsrequest@fortrea.com. Please note that this e-mail address is only for job seekers requesting an accommodation. Please do not use this e-mail to check the status of your application.</div>

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in ~100 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
Are you ready to launch your career in technology?
Our 12-week hybrid paid internship offers hands-on experience in our Global Technology Transformation Office, where you’ll collaborate with IT Infrastructure & Operations experts on impactful tech initiatives.
Gain exposure to emerging technologies such as cloud computing, AI, machine learning, cybersecurity, technical project management, and agile software development. Beyond technical skills, you’ll benefit from career development workshops, executive mentorship, and team-building challenges to prepare for a successful future.
Internship Assignment Summary:
Modern workplace – user experience technology transformation
Technical debt and application modernization transformation
Cloud center of excellence formation
IT Service operation center of excellence sustainability
Main Requirements:
Degree focused on Computer Science, Computer Engineering, Computer Information Systems, IT Security, Informatics, Information Science/Technology, Management Information Systems, Software Engineering, Security and Risk Analysis, or other relevant STEM majors with Software/IT experience
Up to date with current industry standards, trending software, and information technology development tools
Ability to learn quickly and successfully navigate in a fast-paced environment
Proactively learns new tools and identifies opportunities for improvement and promotes their adoption
Contributes to creative solutions and challenges the status quo
Strong customer focus, ability to understand the value proposition for the customer, and commitment to deliver the best value proposition
Able to engage positively across multiple departments to establish clarity, vision, and mutual trust to achieve business goals
Qualifications (Minimum Required):
Degree focused on Computer Science, Computer Engineering, Computer Information Systems, IT Security, Informatics, Information Science/Technology, Management Information Systems, Software Engineering, Security and Risk Analysis.
Relevant STEM majors with Software/IT experience.
This program is designed for students in STEM + Healthcare disciplines, offering real-world assignments that are both challenging and valuable to our organization.
If you’re eager to work on cutting-edge technology projects and make a difference in the industry, this is your opportunity!
#LI-MI1
#LI-Hybrid
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
Fortrea is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement.
If, as a result of a disability, you require a reasonable accommodation to complete your job application, pre-employment testing, job interview or to otherwise participate in the hiring process, please contact: taaccommodationsrequest@fortrea.com. Please note that this e-mail address is only for job seekers requesting an accommodation. Please do not use this e-mail to check the status of your application.

IT Analyst - Internship Program - Hybrid Role / Durham US - Fortrea

IT Analyst - Internship Program - Hybrid Role / Durham US

You need 7+ years in data management/database programming, 5+ years in RAVE/Inform, strong problem-solving skills, protocol interpretation experience, and ability to mentor others.

You will design eCRFs, oversee project work, mentor staff, ensure quality control, manage specifications, consult on database development, and improve EDC processes while maintaining compliance.

<div>As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in ~100 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
Lead Technical Designer &ndash; Medidata RAVE and Inform EDC
Join our growing team and discover your extraordinary potential by working as a Lead Technical Designer within our division, working with some of our most important sponsors. The position offers a strong support network, flexible working solutions and the opportunity to progress your career. This is a permanent, full-time office or home-based role anywhere within Europe and South Africa in the listed countries.
In a client-facing and project management focused role, you will lead eCRF design within the scope of assigned projects. We are looking for an experienced RAVE database designer who has good specification writing experience. Experience with Inform/Veeva EDC beneficial.
What you can expect from us:<ul><li>
Office based or home based anywhere in Europe or South Africa (listed countries)</li><li>
Rewarding and meaningful work in an established, diverse, highly profitable and respected global company</li><li>
Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances etc.</li><li>
A genuine work life balance</li><li>
Flexibility in working hours</li><li>
A thorough onboarding with support from your personal mentor</li><li>
A permanent employment contract with Fortrea</li></ul>
Your responsibilities:<ul><li>
Development and implementation of solutions to global technical service issues and concerns regarding EDC tools like Medidata RAVE and Oracle Inform</li><li>
Responsible for designing the eCRF in leading EDC systems including Rave, Veeva, Inform or other EDC systems</li><li>
Responsible for the preparation and /or review draft and final eCRF, edit check specifications for assigned projects to ensure quality and consistency</li><li>
Follow attention to detail approach and participate in sponsor meetings and audits/inspections</li><li>
Assign tasks and responsibilities to team members, in a manner that: optimizes team capability; delivers timely and accurate results; and supports the needs of the business</li><li>
Assist Managers in data collection for productivity, Quality, timelines and resource planning</li><li>
Responsible for performing quality control procedures for specification development</li><li>
Conducts team meetings and provide guidance to Programmers and Data managers</li><li>
Responsible for maintaining study specifications for assigned projects</li><li>
Responsible for conducting Quality Control of study design for assigned projects</li><li>
Participate in the validation of EDC studies when requested</li><li>
Responsible for the creation and maintenance of library objects within the Global Libraries</li><li>
Responsible for ensuring compliance of standard objects usage throughout the business</li><li>
Perform all activities related to specification development for study build and design of databases according to Standard procedures</li><li>
Responsible for the review and approval of derivations and edit checks requested by the project teams</li><li>
Mentor the study team in CRF Design and specification development for leading EDC databases</li><li>
Oversees the project work of junior staff</li><li>
Mentor and aide in staff development, and achievement of competency standards</li><li>
Assist with the development of training programs to ensure staff, project and technical, achievement of position competencies</li><li>
Present training programs to the technical staff regarding study build, standards maintenance, and/or change control</li><li>
Notify project leadership of requests for out-of-scope work and advise management of changes in scope of projects to enable the timely development of change orders</li><li>
Responsible for meeting with the data manager on assigned projects to discuss technical 
strategies, contractual obligations and timelines. Escalate resource needs as appropriate</li><li>
Provide consultation in the area of database design and development with data managers</li><li>
Provide feedback to management on the development potential of staff to assist in staff 
development</li><li>
Maintain awareness of new developments in EDC vendor products which may be applied to 
improve the efficient use of these systems</li><li>
Implement processes as they are refined, or as new processes are developed and initiate and 
participate in the ongoing review of the processes to ensure they are continually improved</li></ul>
Your profile:<ul><li>
Good knowledge of drug development process and Clinical Data Management Programming</li><li>
Previous relevant work experience to include data management and database support: EDC systems programming or SAS programming</li><li>
You have previous experience of protocol interpretation skills &amp; building/programming databases in RAVE</li><li>
Candidates must be fluent in English language (both verbal and written)</li><li>
Medidata RAVE and protocol interpretation experience strongly preferred</li></ul><ul><li>
Technical expertise: Design Screens &amp; Program Edits in RAVE and Inform</li><li>
Good problem solving skills and a proactive approach</li><li>
Good oral and written communication skills</li><li>
Good knowledge of clinical trial process and data management, biometrics, and systems applications to support operations preferred</li><li>
Ability to work in a team environment</li><li>
Ability to work effectively under minimal supervision</li><li>
Ability to mentor and train the team members</li><li>
Good time management skills and the ability to work to tight deadlines whilst maintain the highest standards of quality work</li><li>
Candidates must be fluent in English language (both verbal and written).</li><li>
Minimum 7 years of relevant work experience to include data management and/or database programming and spec design activities, including 5 years in Medidata Rave, Oracle Inform, Veeva</li></ul> 
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
Fortrea is proud to be an Equal Opportunity Employer: 
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement.
If, as a result of a disability, you require a reasonable accommodation to complete your job application, pre-employment testing, job interview or to otherwise participate in the hiring process, please contact: taaccommodationsrequest@fortrea.com. Please note that this e-mail address is only for job seekers requesting an accommodation. Please do not use this e-mail to check the status of your application.</div>

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in ~100 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
Lead Technical Designer – Medidata RAVE and Inform EDC
Join our growing team and discover your extraordinary potential by working as a Lead Technical Designer within our division, working with some of our most important sponsors. The position offers a strong support network, flexible working solutions and the opportunity to progress your career. This is a permanent, full-time office or home-based role anywhere within Europe and South Africa in the listed countries.
In a client-facing and project management focused role, you will lead eCRF design within the scope of assigned projects. We are looking for an experienced RAVE database designer who has good specification writing experience. Experience with Inform/Veeva EDC beneficial.
What you can expect from us:
Office based or home based anywhere in Europe or South Africa (listed countries)
Rewarding and meaningful work in an established, diverse, highly profitable and respected global company
Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances etc.
A genuine work life balance
Flexibility in working hours
A thorough onboarding with support from your personal mentor
A permanent employment contract with Fortrea
Your responsibilities:
Development and implementation of solutions to global technical service issues and concerns regarding EDC tools like Medidata RAVE and Oracle Inform
Responsible for designing the eCRF in leading EDC systems including Rave, Veeva, Inform or other EDC systems
Responsible for the preparation and /or review draft and final eCRF, edit check specifications for assigned projects to ensure quality and consistency
Follow attention to detail approach and participate in sponsor meetings and audits/inspections
Assign tasks and responsibilities to team members, in a manner that: optimizes team capability; delivers timely and accurate results; and supports the needs of the business
Assist Managers in data collection for productivity, Quality, timelines and resource planning
Responsible for performing quality control procedures for specification development
Conducts team meetings and provide guidance to Programmers and Data managers
Responsible for maintaining study specifications for assigned projects
Responsible for conducting Quality Control of study design for assigned projects
Participate in the validation of EDC studies when requested
Responsible for the creation and maintenance of library objects within the Global Libraries
Responsible for ensuring compliance of standard objects usage throughout the business
Perform all activities related to specification development for study build and design of databases according to Standard procedures
Responsible for the review and approval of derivations and edit checks requested by the project teams
Mentor the study team in CRF Design and specification development for leading EDC databases
Oversees the project work of junior staff
Mentor and aide in staff development, and achievement of competency standards
Assist with the development of training programs to ensure staff, project and technical, achievement of position competencies
Present training programs to the technical staff regarding study build, standards maintenance, and/or change control
Notify project leadership of requests for out-of-scope work and advise management of changes in scope of projects to enable the timely development of change orders
Responsible for meeting with the data manager on assigned projects to discuss technical
strategies, contractual obligations and timelines. Escalate resource needs as appropriate
Provide consultation in the area of database design and development with data managers
Provide feedback to management on the development potential of staff to assist in staff
development
Maintain awareness of new developments in EDC vendor products which may be applied to
improve the efficient use of these systems
Implement processes as they are refined, or as new processes are developed and initiate and
participate in the ongoing review of the processes to ensure they are continually improved
Your profile:
Good knowledge of drug development process and Clinical Data Management Programming
Previous relevant work experience to include data management and database support: EDC systems programming or SAS programming
You have previous experience of protocol interpretation skills & building/programming databases in RAVE
Candidates must be fluent in English language (both verbal and written)
Medidata RAVE and protocol interpretation experience strongly preferred
Technical expertise: Design Screens & Program Edits in RAVE and Inform
Good problem solving skills and a proactive approach
Good oral and written communication skills
Good knowledge of clinical trial process and data management, biometrics, and systems applications to support operations preferred
Ability to work in a team environment
Ability to work effectively under minimal supervision
Ability to mentor and train the team members
Good time management skills and the ability to work to tight deadlines whilst maintain the highest standards of quality work
Candidates must be fluent in English language (both verbal and written).
Minimum 7 years of relevant work experience to include data management and/or database programming and spec design activities, including 5 years in Medidata Rave, Oracle Inform, Veeva
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
Fortrea is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement.
If, as a result of a disability, you require a reasonable accommodation to complete your job application, pre-employment testing, job interview or to otherwise participate in the hiring process, please contact: taaccommodationsrequest@fortrea.com. Please note that this e-mail address is only for job seekers requesting an accommodation. Please do not use this e-mail to check the status of your application.

Fortrea

Mission