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MCRA is the leading global full-service medical device, diagnostics, and biologics CRO and consulting advisory firm. MCRA delivers to its client’s industry experience, integrating its seven business value creators: regulatory, clinical research, reimbursement, healthcare compliance, quality assurance, due diligence and distribution logistics to provide a dynamic, market-leading effort from innovation conception to commercialization. MCRA’s integrated application of these key value-creating initiatives provides unparalleled value for its clients. MCRA has offices in Washington, DC, Hartford, CT, New York, NY, London, England, Winterthur, Switzerland, Eschborn, Germany and Tokyo, Japan and serves nearly 1,000 clients globally. Its core focus areas of therapeutic experience include orthopedics, spine, biologics, cardiovascular, diagnostic imaging, wound care, artificial intelligence, dental, anesthesia, general surgery, digital health, neurology, robotics, oncology, general and plastic surgery, urology, and in vitro diagnostic (IVD) devices and medical device cybersecurity. MCRA places particular emphasis on its expertise working with companies in all stages of development and throughout the technology life cycle by ushering technologies from the conceptual pre-clinical stage to market approval.


Manufacturing & Electronics

MCRA

Leading Global Full-Service Medical Device, Diagnostics & Biologics CRO & Integrated Consulting Advisory Firm.

Science & Healthcare

You should be a Bioengineering, Chemical Engineering, Materials Science, Chemistry, or MPH student, an incoming Junior/Senior, with skills in scientific reading, writing, and materials science.

You will assist in creating a database predicting chemical leaching from medical devices, analyzing data on materials, and identifying toxic compounds to support biocompatibility strategies.

Research & Development

Healthcare

Washington

<div><div>MCRA, an IQVIA business, is a leading medical device advisory firm and clinical research organization (CRO). MCRA's value contribution rests within its industry experience at integrating five business value creators&mdash;regulatory, clinical research, reimbursement, healthcare compliance, and quality assurance&mdash;to provide a dynamic, market-leading effort from concept to commercialization. MCRA's integrated application of these key value-creating functions provides unparalleled expertise for its clients. MCRA has offices in Washington, DC, Manchester, CT, New York, NY, and a global presence in Japan and Europe and serves more than 1500 clients globally. Its core focus areas of therapeutic experience include orthopedics, spine, cardiovascular, neurology, digital health, diagnostic imaging, wound care, dental, general healthcare, robotics, and in vitro diagnostic (IVD) devices.</div><div></div><div><b><br>
Intern Duties</b></div><div>
Interns will work closely with MCRA experts and mentors to gain critical hands-on knowledge in Regulatory Affairs, Biocompatibility, and Toxicology.<br>
</div><div></div><br>
<div>The goal of this project would be to create a comprehensive database that predicts potential chemical leaching from medical devices based on material composition. The project will require the intern to collect and analyze data from chemical characterization studies conducted on a wide range of devices made from various materials. Specifically, the project will aim to identify toxicologically relevant compounds that may leach from commonly used medical device manufacturing materials. This database will be used in developing biocompatibility strategies for current and future clients.</div><div>
</div>
<h3 class="jobSectionHeader"><b>Skills and Qualifications:
</b></h3><ul><li>Currently pursuing Bioengineer; Chemical Engineer; Materials Science; Chemistry; Master of Public Health.</li><li>
Incoming Junior or Senior.</li><li>
Experience with reading scientific papers; experience with scientific writing; materials science knowledge.</li></ul><h3 class="jobSectionHeader"><b>
Internship Program Details:</b></h3><ul><li>
Duration: 8 Weeks (June 2, 2025 &ndash; July 25, 2025).</li><li>
Hours: 25 hours per week, 5 hours per day (approx. 9:00am-3:00pm daily &ndash; specific schedules may vary).</li><li>
Location: DC-Based hybrid schedule</li><li>
A laptop and other required equipment will be provided.</li></ul><div><b>
NOTE: </b>This job description is not intended to be all-inclusive. Employee may perform other related duties as to meet the ongoing needs of the organization.
</div><div><b>
</b></div><div><b>MCRA, an IQVIA business, is an equal opportunity/Affirmative Action employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, political affiliation, sexual orientation, gender identity, marital status, disability, protected veteran status, genetic information, age, or other legally protected characteristics.</b></div></div>

MCRA, an IQVIA business, is a leading medical device advisory firm and clinical research organization (CRO). MCRA's value contribution rests within its industry experience at integrating five business value creators—regulatory, clinical research, reimbursement, healthcare compliance, and quality assurance—to provide a dynamic, market-leading effort from concept to commercialization. MCRA's integrated application of these key value-creating functions provides unparalleled expertise for its clients. MCRA has offices in Washington, DC, Manchester, CT, New York, NY, and a global presence in Japan and Europe and serves more than 1500 clients globally. Its core focus areas of therapeutic experience include orthopedics, spine, cardiovascular, neurology, digital health, diagnostic imaging, wound care, dental, general healthcare, robotics, and in vitro diagnostic (IVD) devices.
Intern Duties
Interns will work closely with MCRA experts and mentors to gain critical hands-on knowledge in Regulatory Affairs, Biocompatibility, and Toxicology.

The goal of this project would be to create a comprehensive database that predicts potential chemical leaching from medical devices based on material composition. The project will require the intern to collect and analyze data from chemical characterization studies conducted on a wide range of devices made from various materials. Specifically, the project will aim to identify toxicologically relevant compounds that may leach from commonly used medical device manufacturing materials. This database will be used in developing biocompatibility strategies for current and future clients.

Skills and Qualifications:
Currently pursuing Bioengineer; Chemical Engineer; Materials Science; Chemistry; Master of Public Health.
Incoming Junior or Senior.
Experience with reading scientific papers; experience with scientific writing; materials science knowledge.
Internship Program Details:
Duration: 8 Weeks (June 2, 2025 – July 25, 2025).
Hours: 25 hours per week, 5 hours per day (approx. 9:00am-3:00pm daily – specific schedules may vary).
Location: DC-Based hybrid schedule
A laptop and other required equipment will be provided.
NOTE: This job description is not intended to be all-inclusive. Employee may perform other related duties as to meet the ongoing needs of the organization.

MCRA, an IQVIA business, is an equal opportunity/Affirmative Action employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, political affiliation, sexual orientation, gender identity, marital status, disability, protected veteran status, genetic information, age, or other legally protected characteristics.

Intern, Regulatory Affairs (Biocompatibility) - MCRA

Intern, Regulatory Affairs (Biocompatibility)

You should be pursuing Biomedical Engineering or Data Science, be an incoming Junior or Senior, and have knowledge of OneNote, good organizational skills, and an interest in knowledge management.

You will collaborate with experts, gain hands-on regulatory knowledge in neurology, conduct research, and develop a resource for project execution and knowledge management across therapies.

<div><div>MCRA, an IQVIA business, is a leading medical device advisory firm and clinical research organization (CRO). MCRA's value contribution rests within its industry experience at integrating five business value creators&mdash;regulatory, clinical research, reimbursement, healthcare compliance, and quality assurance&mdash;to provide a dynamic, market-leading effort from concept to commercialization. MCRA's integrated application of these key value-creating functions provides unparalleled expertise for its clients. MCRA has offices in Washington, DC, Manchester, CT, New York, NY, and a global presence in Japan and Europe and serves more than 1500 clients globally. Its core focus areas of therapeutic experience include orthopedics, spine, cardiovascular, neurology, digital health, diagnostic imaging, wound care, dental, general healthcare, robotics, and in vitro diagnostic (IVD) devices.</div><div></div><div><b><br>
Intern Duties</b></div><div>
Interns will work closely with MCRA experts and mentors to gain critical hands-on knowledge in Regulatory Affairs, Neurology.<br>
</div><div></div><br>
<div>Interns will work closely with MCRA experts and mentors to gain critical hands-on knowledge in Regulatory Affairs &ndash; Neuro. Interns will research a specific topic and complete a meaningful project presentation. Potential projects topics include:</div><ul><li> Assist with developing a unified resource for project execution and knowledge management that can be used across therapies within regulatory and across future service areas.</li></ul><div>
</div>
<h3 class="jobSectionHeader"><b>Skills and Qualifications:
</b></h3><ul><li>Currently pursuing Biomedical engineering or Data science.
</li><li>Incoming Junior or Senior.</li><li>
Knowledge of OneNote, interest in knowledge management, and good organizational skills.</li></ul><h3 class="jobSectionHeader"><b>
Internship Program Details:</b></h3><ul><li>
Duration: 8 Weeks (June 2, 2025 &ndash; July 25, 2025).</li><li>
Hours: 25 hours per week, 5 hours per day (approx. 9:00am-3:00pm daily &ndash; specific schedules may vary).</li><li>
Location: DC-Based hybrid schedule</li><li>
A laptop and other required equipment will be provided.</li></ul><div><b>
NOTE: </b>This job description is not intended to be all-inclusive. Employee may perform other related duties as to meet the ongoing needs of the organization.
</div><div><b>
</b></div><div><b>MCRA, an IQVIA business, is an equal opportunity/Affirmative Action employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, political affiliation, sexual orientation, gender identity, marital status, disability, protected veteran status, genetic information, age, or other legally protected characteristics.</b></div></div>

MCRA, an IQVIA business, is a leading medical device advisory firm and clinical research organization (CRO). MCRA's value contribution rests within its industry experience at integrating five business value creators—regulatory, clinical research, reimbursement, healthcare compliance, and quality assurance—to provide a dynamic, market-leading effort from concept to commercialization. MCRA's integrated application of these key value-creating functions provides unparalleled expertise for its clients. MCRA has offices in Washington, DC, Manchester, CT, New York, NY, and a global presence in Japan and Europe and serves more than 1500 clients globally. Its core focus areas of therapeutic experience include orthopedics, spine, cardiovascular, neurology, digital health, diagnostic imaging, wound care, dental, general healthcare, robotics, and in vitro diagnostic (IVD) devices.
Intern Duties
Interns will work closely with MCRA experts and mentors to gain critical hands-on knowledge in Regulatory Affairs, Neurology.

Interns will work closely with MCRA experts and mentors to gain critical hands-on knowledge in Regulatory Affairs – Neuro. Interns will research a specific topic and complete a meaningful project presentation. Potential projects topics include: Assist with developing a unified resource for project execution and knowledge management that can be used across therapies within regulatory and across future service areas.

Skills and Qualifications:
Currently pursuing Biomedical engineering or Data science.
Incoming Junior or Senior.
Knowledge of OneNote, interest in knowledge management, and good organizational skills.
Internship Program Details:
Duration: 8 Weeks (June 2, 2025 – July 25, 2025).
Hours: 25 hours per week, 5 hours per day (approx. 9:00am-3:00pm daily – specific schedules may vary).
Location: DC-Based hybrid schedule
A laptop and other required equipment will be provided.
NOTE: This job description is not intended to be all-inclusive. Employee may perform other related duties as to meet the ongoing needs of the organization.

MCRA, an IQVIA business, is an equal opportunity/Affirmative Action employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, political affiliation, sexual orientation, gender identity, marital status, disability, protected veteran status, genetic information, age, or other legally protected characteristics.

Intern, Regulatory Affairs (Neurology) - MCRA

Intern, Regulatory Affairs (Neurology)

You should be a Junior or Senior in Biological Sciences or Engineering, with skills in PowerPoint, Excel, strong writing, analytics, and be comfortable giving presentations.

You will assist in task analysis and risk assessment for medical devices, develop use scenarios, and create templates based on IEC 62366 and FDA guidelines for usability studies.

<div><div>MCRA, an IQVIA business, is a leading medical device advisory firm and clinical research organization (CRO). MCRA's value contribution rests within its industry experience at integrating five business value creators&mdash;regulatory, clinical research, reimbursement, healthcare compliance, and quality assurance&mdash;to provide a dynamic, market-leading effort from concept to commercialization. MCRA's integrated application of these key value-creating functions provides unparalleled expertise for its clients. MCRA has offices in Washington, DC, Manchester, CT, New York, NY, and a global presence in Japan and Europe and serves more than 1500 clients globally. Its core focus areas of therapeutic experience include orthopedics, spine, cardiovascular, neurology, digital health, diagnostic imaging, wound care, dental, general healthcare, robotics, and in vitro diagnostic (IVD) devices.</div><div></div><div><b><br>
Intern Duties</b></div><div>
Interns will work closely with MCRA experts and mentors to gain critical hands-on knowledge in Regulatory Affairs, Digital Health.<br>
</div><div></div><br>
<div>Usability study design usually starts with a task analysis which breaks down the workflow of using a device into individual tasks and assess the potential use errors pertaining to each task along with the resulted harms from said use errors. The process of task analysis should not be streamlined for devices with a dynamic or flexible workflow, such as software devices with various modalities and functions. A streamlined task analysis and use scenarios do not appreciate the possibility of a dynamic workflow where user is able to go back and forth in interfaces and prioritize certain modality over others in actual use scenarios. The use-related risks from the flexibility of the interface would be easily left out in the risk analysis.</div><div></div><div><br>
In this project, we will experiment various ways of task analysis and use-related risk analysis to find the best presentation of use scenarios for medical devices with a flexible workflow. The project will base on a case analysis of an SaMD (software as medical device), followed by an analysis of the applicability of the results to other types of devices.<br>
</div><div></div><br>
<div>The intern can expect to learn to do task analysis and use related risk analysis according to IEC 62366 and FDA 2016 guidance on usability engineering, and get hand on experience in developing use scenarios for a usability study. The deliverable of the project will be templates for presenting the task analysis, use-related risk analysis, and use scenario for devices with complicated workflows.</div><div>
</div>
<h3 class="jobSectionHeader"><b>Skills and Qualifications:
</b></h3><ul><li>Currently pursuing any of the Biological Sciences or Engineering disciplines.
</li><li>Incoming Junior, or Senior</li><li>
Proficiency in PowerPoint and Excel, strong writing and analytical skills, comfortable with giving presentations.</li></ul><h3 class="jobSectionHeader"><b>
Internship Program Details:</b></h3><ul><li>
Duration: 8 Weeks (June 2, 2025 &ndash; July 25, 2025).</li><li>
Hours: 25 hours per week, 5 hours per day (approx. 9:00am-3:00pm daily &ndash; specific schedules may vary).</li><li>
Location: DC-Based hybrid schedule</li><li>
A laptop and other required equipment will be provided.</li></ul><div><b>
NOTE: </b>This job description is not intended to be all-inclusive. Employee may perform other related duties as to meet the ongoing needs of the organization.
</div><div><b>
</b></div><div><b>MCRA, an IQVIA business, is an equal opportunity/Affirmative Action employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, political affiliation, sexual orientation, gender identity, marital status, disability, protected veteran status, genetic information, age, or other legally protected characteristics.</b></div></div>

MCRA, an IQVIA business, is a leading medical device advisory firm and clinical research organization (CRO). MCRA's value contribution rests within its industry experience at integrating five business value creators—regulatory, clinical research, reimbursement, healthcare compliance, and quality assurance—to provide a dynamic, market-leading effort from concept to commercialization. MCRA's integrated application of these key value-creating functions provides unparalleled expertise for its clients. MCRA has offices in Washington, DC, Manchester, CT, New York, NY, and a global presence in Japan and Europe and serves more than 1500 clients globally. Its core focus areas of therapeutic experience include orthopedics, spine, cardiovascular, neurology, digital health, diagnostic imaging, wound care, dental, general healthcare, robotics, and in vitro diagnostic (IVD) devices.
Intern Duties
Interns will work closely with MCRA experts and mentors to gain critical hands-on knowledge in Regulatory Affairs, Digital Health.

Usability study design usually starts with a task analysis which breaks down the workflow of using a device into individual tasks and assess the potential use errors pertaining to each task along with the resulted harms from said use errors. The process of task analysis should not be streamlined for devices with a dynamic or flexible workflow, such as software devices with various modalities and functions. A streamlined task analysis and use scenarios do not appreciate the possibility of a dynamic workflow where user is able to go back and forth in interfaces and prioritize certain modality over others in actual use scenarios. The use-related risks from the flexibility of the interface would be easily left out in the risk analysis.
In this project, we will experiment various ways of task analysis and use-related risk analysis to find the best presentation of use scenarios for medical devices with a flexible workflow. The project will base on a case analysis of an SaMD (software as medical device), followed by an analysis of the applicability of the results to other types of devices.

The intern can expect to learn to do task analysis and use related risk analysis according to IEC 62366 and FDA 2016 guidance on usability engineering, and get hand on experience in developing use scenarios for a usability study. The deliverable of the project will be templates for presenting the task analysis, use-related risk analysis, and use scenario for devices with complicated workflows.

Skills and Qualifications:
Currently pursuing any of the Biological Sciences or Engineering disciplines.
Incoming Junior, or Senior
Proficiency in PowerPoint and Excel, strong writing and analytical skills, comfortable with giving presentations.
Internship Program Details:
Duration: 8 Weeks (June 2, 2025 – July 25, 2025).
Hours: 25 hours per week, 5 hours per day (approx. 9:00am-3:00pm daily – specific schedules may vary).
Location: DC-Based hybrid schedule
A laptop and other required equipment will be provided.
NOTE: This job description is not intended to be all-inclusive. Employee may perform other related duties as to meet the ongoing needs of the organization.

MCRA, an IQVIA business, is an equal opportunity/Affirmative Action employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, political affiliation, sexual orientation, gender identity, marital status, disability, protected veteran status, genetic information, age, or other legally protected characteristics.

Intern, Regulatory Affairs (Digital Health) - MCRA

Intern, Regulatory Affairs (Digital Health)

You must be a current undergrad pursuing a Business Administration or related degree, and be an incoming Junior or Senior.

You will learn MedTech issues, enhance decision-making and project management skills, and update clinical study statistics while expanding into regulatory affairs.

Business, Operations & Strategy

<div><div>MCRA, an IQVIA business, is a leading medical device advisory firm and clinical research organization (CRO). MCRA's value contribution rests within its industry experience at integrating five business value creators&mdash;regulatory, clinical research, reimbursement, healthcare compliance, and quality assurance&mdash;to provide a dynamic, market-leading effort from concept to commercialization. MCRA's integrated application of these key value-creating functions provides unparalleled expertise for its clients. MCRA has offices in Washington, DC, Manchester, CT, New York, NY, and a global presence in Japan and Europe and serves more than 1500 clients globally. Its core focus areas of therapeutic experience include orthopedics, spine, cardiovascular, neurology, digital health, diagnostic imaging, wound care, dental, general healthcare, robotics, and in vitro diagnostic (IVD) devices.</div><div></div><div><br>
Interns will work closely with MCRA experts and mentors to gain critical hands-on knowledge in Business Development. Interns will research a specific topic and complete a meaningful project presentation.<br>
</div><div></div><br>
<div>During the internship you will learn to demonstrate an in-depth understanding of critical issues and topics in the MedTech and Medical Device world. You will develop decision-making, and project management skills while leveraging strong problem-solving, organizational, communication, and analytical skills. The intern will be responsible for updating all of our clinical study statistics and track record and expanding into regulatory affairs as well.</div><br>
<div></div>
<h3 class="jobSectionHeader"><b>
Qualifications</b></h3><ul><li>
Current undergrad student (pursuing a degree in Business Administration or industry related is preferred)</li><li>
Incoming Junior or Senior</li></ul><h3 class="jobSectionHeader"><b>
Summer Internship Program Details
</b></h3><ul><li>Duration: 8 Weeks (June 2, 2025 &ndash; July 25, 2025).</li><li>
Hours: 25 hours per week, 5 hours per day (approx. 9:00am-3:00pm daily &ndash; specific schedules may vary).</li><li>
Location: DC-Based hybrid schedule
</li><li>A laptop and other required equipment will be provided.</li></ul><div><b>
NOTE: </b>This job description is not intended to be all-inclusive. Employee may perform other related duties as to meet the ongoing needs of the organization.
</div><div><b>
</b></div><div><b>MCRA, an IQVIA business, is an equal opportunity/Affirmative Action employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, political affiliation, sexual orientation, gender identity, marital status, disability, protected veteran status, genetic information, age, or other legally protected characteristics.</b></div></div>

MCRA, an IQVIA business, is a leading medical device advisory firm and clinical research organization (CRO). MCRA's value contribution rests within its industry experience at integrating five business value creators—regulatory, clinical research, reimbursement, healthcare compliance, and quality assurance—to provide a dynamic, market-leading effort from concept to commercialization. MCRA's integrated application of these key value-creating functions provides unparalleled expertise for its clients. MCRA has offices in Washington, DC, Manchester, CT, New York, NY, and a global presence in Japan and Europe and serves more than 1500 clients globally. Its core focus areas of therapeutic experience include orthopedics, spine, cardiovascular, neurology, digital health, diagnostic imaging, wound care, dental, general healthcare, robotics, and in vitro diagnostic (IVD) devices.
Interns will work closely with MCRA experts and mentors to gain critical hands-on knowledge in Business Development. Interns will research a specific topic and complete a meaningful project presentation.

During the internship you will learn to demonstrate an in-depth understanding of critical issues and topics in the MedTech and Medical Device world. You will develop decision-making, and project management skills while leveraging strong problem-solving, organizational, communication, and analytical skills. The intern will be responsible for updating all of our clinical study statistics and track record and expanding into regulatory affairs as well.


Qualifications
Current undergrad student (pursuing a degree in Business Administration or industry related is preferred)
Incoming Junior or Senior
Summer Internship Program Details
Duration: 8 Weeks (June 2, 2025 – July 25, 2025).
Hours: 25 hours per week, 5 hours per day (approx. 9:00am-3:00pm daily – specific schedules may vary).
Location: DC-Based hybrid schedule
A laptop and other required equipment will be provided.
NOTE: This job description is not intended to be all-inclusive. Employee may perform other related duties as to meet the ongoing needs of the organization.

MCRA, an IQVIA business, is an equal opportunity/Affirmative Action employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, political affiliation, sexual orientation, gender identity, marital status, disability, protected veteran status, genetic information, age, or other legally protected characteristics.

Intern, Business Development - MCRA

Intern, Business Development

You must be pursuing a bachelor's in biomedical, social sciences, bioengineering, or clinical research, be a junior or senior, and be proficient in Microsoft applications with strong research skills.

You will develop strategies for site identification, ensure compliance, track enrollment, manage meeting agendas, and assist with various study operations tasks.

<div><div>MCRA, an IQVIA business, is a leading medical device advisory firm and clinical research organization (CRO). MCRA's value contribution rests within its industry experience at integrating five business value creators&mdash;regulatory, clinical research, reimbursement, healthcare compliance, and quality assurance&mdash;to provide a dynamic, market-leading effort from concept to commercialization. MCRA's integrated application of these key value-creating functions provides unparalleled expertise for its clients. MCRA has offices in Washington, DC, Manchester, CT, New York, NY, and a global presence in Japan and Europe and serves more than 1500 clients globally. Its core focus areas of therapeutic experience include orthopedics, spine, cardiovascular, neurology, digital health, diagnostic imaging, wound care, dental, general healthcare, robotics, and in vitro diagnostic (IVD) devices.</div><div></div><div><br>
Interns will work closely with MCRA experts and mentors to gain critical hands-on knowledge in Clinical Affairs. Interns will research a specific topic and complete a meaningful project presentation. Potential projects topics include:</div><ul><li> Developing innovative strategies for site identification, risk mitigation, and subject recruitment/retention.</li><li> Assuring compliance with SOPs and local regulations, and CFR, ICH, and GCP guidelines</li><li> Enrollment tracking, maintenance, and mitigation</li><li> Developing weekly meetings agendas and summary minutes</li><li> Assist with other tasks within study operations.</li></ul>
<h3 class="jobSectionHeader"><b>Skills and Qualifications:</b></h3><ul><li>
Currently pursuing a bachelor&rsquo;s degree in biomedical, Social Sciences, Bioengineering, or Clinical Research.</li><li>
Incoming Junior or Senior.
</li><li>Proficient in all Microsoft applications</li><li>
Strong research skills, self-motivated, and strong attention to detail.</li></ul><h3 class="jobSectionHeader"><b>
Internship Program Details:</b></h3><ul><li>
Duration: 8 Weeks (June 2, 2025 &ndash; July 25, 2025).</li><li>
Hours: 25 hours per week, 5 hours per day (approx. 9:00am-3:00pm daily &ndash; specific schedules may vary).</li><li>
Location: DC-Based hybrid schedule
</li><li>A laptop and other required equipment will be provided.</li></ul><div><b>
NOTE: </b>This job description is not intended to be all-inclusive. Employee may perform other related duties as to meet the ongoing needs of the organization.
</div><div><b>
</b></div><div><b>MCRA, an IQVIA business, is an equal opportunity/Affirmative Action employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, political affiliation, sexual orientation, gender identity, marital status, disability, protected veteran status, genetic information, age, or other legally protected characteristics.</b></div></div>

MCRA, an IQVIA business, is a leading medical device advisory firm and clinical research organization (CRO). MCRA's value contribution rests within its industry experience at integrating five business value creators—regulatory, clinical research, reimbursement, healthcare compliance, and quality assurance—to provide a dynamic, market-leading effort from concept to commercialization. MCRA's integrated application of these key value-creating functions provides unparalleled expertise for its clients. MCRA has offices in Washington, DC, Manchester, CT, New York, NY, and a global presence in Japan and Europe and serves more than 1500 clients globally. Its core focus areas of therapeutic experience include orthopedics, spine, cardiovascular, neurology, digital health, diagnostic imaging, wound care, dental, general healthcare, robotics, and in vitro diagnostic (IVD) devices.
Interns will work closely with MCRA experts and mentors to gain critical hands-on knowledge in Clinical Affairs. Interns will research a specific topic and complete a meaningful project presentation. Potential projects topics include: Developing innovative strategies for site identification, risk mitigation, and subject recruitment/retention. Assuring compliance with SOPs and local regulations, and CFR, ICH, and GCP guidelines Enrollment tracking, maintenance, and mitigation Developing weekly meetings agendas and summary minutes Assist with other tasks within study operations.
Skills and Qualifications:
Currently pursuing a bachelor’s degree in biomedical, Social Sciences, Bioengineering, or Clinical Research.
Incoming Junior or Senior.
Proficient in all Microsoft applications
Strong research skills, self-motivated, and strong attention to detail.
Internship Program Details:
Duration: 8 Weeks (June 2, 2025 – July 25, 2025).
Hours: 25 hours per week, 5 hours per day (approx. 9:00am-3:00pm daily – specific schedules may vary).
Location: DC-Based hybrid schedule
A laptop and other required equipment will be provided.
NOTE: This job description is not intended to be all-inclusive. Employee may perform other related duties as to meet the ongoing needs of the organization.

MCRA, an IQVIA business, is an equal opportunity/Affirmative Action employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, political affiliation, sexual orientation, gender identity, marital status, disability, protected veteran status, genetic information, age, or other legally protected characteristics.

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