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

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Fortrea

Mar 2

  • Job
    Full-time
    Junior, Mid & Senior Level
  • Research & Development
    Healthcare
  • Germany
    Remote

AI generated summary

  • 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.

Requirements

  • 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

Responsibilities

  • 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

FAQs

Do we support remote work?

Yes, this position offers a home-office work arrangement.

What kind of studies will I be working on as a Clinical Research Associate?

You will be involved in the management of complex clinical studies, specifically phases I - III, with a focus on innovative drugs, particularly in the oncology area.

What qualifications are required for this position?

A relevant university degree in fields such as biology, biochemistry, chemistry, health management, pharmacology, or (veterinary) medicine is required, along with independent monitoring experience in clinical studies.

Is there an onboarding process for new employees?

Yes, there is a comprehensive onboarding process supported by a personal mentor.

Are there opportunities for professional development within the company?

Yes, there are excellent training and development opportunities available within Fortrea, as well as support for your personal educational plans.

What languages do I need to be proficient in for this role?

Excellent communication skills in German are required, along with good proficiency in English, both written and spoken.

Does the position involve any travel?

Yes, the role may involve travel, and travel time is considered working time.

What benefits does Fortrea offer to its employees?

Fortrea offers competitive compensation, including a 13th salary and vacation pay, a pension plan, flexible working hours, and a healthy work-life balance.

Is Fortrea an equal opportunity employer?

Yes, Fortrea is an Equal Opportunity Employer committed to diversity and inclusion in the workforce.

Can I get assistance if I require accommodations due to a disability during the hiring process?

Yes, you can contact taaccommodationsrequest@fortrea.com for assistance with reasonable accommodations during the application and hiring process.

Science & Healthcare
Industry
10,001+
Employees
2023
Founded Year

Mission & Purpose

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.