This full-time position offers in-depth training and flexible work—perfect for qualified candidates seeking entry into clinical research careers in Europe. Posted recently (Job ID: R1526021), with start dates on April 1 or 16, 2026.
About the Company
IQVIA is a leading global provider of advanced analytics, clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries.
With a presence in over 100 countries, IQVIA connects intelligent data and technology to accelerate the development and commercialization of innovative medical treatments, improving patient outcomes and population health worldwide.
Known for its sponsor-dedicated models, robust training programs, and commitment to integrity, diversity, and employee development, IQVIA empowers professionals to make a real impact in global clinical trials.
Job Details
- Company Name: IQVIA
- Experience: Trainee/Entry-level (focus on training; prior monitoring not required)
- Qualification: University degree in healthcare or scientific discipline OR vocational education in medical field; completed advanced training in clinical research (mandatory)
- Location: Home-Office throughout Germany (based in Frankfurt/Hesse area for reference)
- Work Type: Full-Time, Home-Based (with business travel up to 40-60%)
Job Description
IQVIA is offering this Trainee Clinical Research Associate role within a sponsor-dedicated Clinical Functional Service Partnership model.
You will work closely with one key pharma client on various clinical trial projects, gaining hands-on experience in site management and trial oversight while receiving structured mentoring and co-monitoring.
Trainee Clinical Research Associate / Associate CRA (m/w/d)
- Department: Clinical Site Management / Clinical Research
- Market: Global Life Sciences (sponsor-dedicated pharma client)
- Role: Trainee Clinical Research Associate
- Experience: Trainee level (advanced clinical research training required)
- Education/Qualification: University degree (healthcare/scientific) or medical vocational training; mandatory completed advanced clinical research training
Skills/Qualifications
- Fluent German (written and verbal) at C1 level or higher (mandatory)
- Good command of English (mandatory)
- Valid driver’s license class B
- Proficiency in Microsoft Word, Excel, and PowerPoint
- Strong organizational, problem-solving, and time management skills
- Ability to handle competing priorities and travel extensively (40-60%)
- Excellent interpersonal skills for building relationships with sites, teams, and clients
- Availability to start on April 1 or 16, 2026 (mandatory)
Key Responsibilities
- Perform site selection, initiation, monitoring, and close-out visits
- Maintain accurate and complete documentation for trial activities
- Support development of subject recruitment plans
- Establish communication lines and deliver protocol/study training to sites
- Evaluate site quality and integrity; escalate issues appropriately
- Track progress including regulatory submissions, recruitment, CRF completion, and query resolution
Benefits/Perks
- Permanent employment contract from day one
- Comprehensive on-the-job training, mentoring, and co-monitoring
- Flexible working schedule with full home-office setup across Germany
- Company car (or allowance), accident insurance, and additional benefits
- Opportunity for career progression in clinical research
- Supportive environment focused on innovation and patient impact
How to Apply
Apply online via the official IQVIA careers portal at https://jobs.iqvia.com. Search for Job ID R1526021 or “Trainee Clinical Research Associate Germany.” Submit your English CV, motivation letter, education certificates, and reference letters (Arbeitszeugnisse).
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the IQVIA Career page.
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For more clinical research, CRA, pharmacovigilance, and pharma opportunities across Europe and India, explore .
Why You Should Join
IQVIA provides an ideal launchpad for aspiring CRAs with its award-winning training, sponsor-dedicated stability, and focus on meaningful advancements in patient health.
Enjoy home-based flexibility in Germany, extensive travel for real-world experience, and long-term growth in a global leader committed to integrity, diversity, and professional development. This role builds strong foundations in clinical trial management within a dynamic, purpose-driven organization.
