Kickstart or advance your clinical research career with Fortrea as a CRA I or II in Germany. This remote role offers hands-on monitoring experience across Oncology, Dermatology, and more. Ideal for early-career professionals seeking pharma jobs and pharmaceutical careers in a global CRO.
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About the Company
Fortrea is a leading global Contract Research Organization (CRO) dedicated to advancing clinical development and bringing life-changing treatments to patients faster. With over 30 years of expertise, Fortrea delivers comprehensive Phase I–IV clinical trial management, clinical pharmacology, and market access solutions to biopharma and MedTech companies worldwide.
Headquartered in the US with operations in approximately 100 countries, the company emphasizes innovation, regulatory compliance, operational excellence, and patient-focused approaches to raise CRO standards.
Job Details
- Company Name: Fortrea
- Experience: Entry-level to 1 year (including internships or up to 12 months onsite monitoring)
- Qualification: University or college degree in life sciences, nursing, pharmacy, or related field
- Location: Munich / Remote Germany
- Work Type: Remote / Full time
Job Description
Fortrea is hiring for upcoming opportunities for Clinical Research Associate I or II (CRA I / CRA II) positions based in Germany. This role provides an excellent entry or early-career step into clinical research, supporting the successful delivery of clinical trials across multiple therapeutic areas under experienced guidance.
Clinical Research Associate I or II
- Department: Clinical Monitoring / Operations
- Market: Global Clinical Development
- Role: Clinical Research Associate (CRA)
- Experience: 0–1 year in clinical research
- Education/Qualification: Life sciences, nursing, pharmacy degree or equivalent
Skills/Qualifications
- University/college degree in life sciences, nursing, pharmacy, or related discipline
- Basic understanding of ICH-GCP guidelines and clinical trial processes
- Entry-level to 1 year of relevant experience (internships or monitoring welcome)
- Fluency in German and English (written and spoken)
- Strong attention to detail and commitment to documentation standards
- Comfort with clinical systems/tools and willingness to travel for site visits
- Ability to work independently while collaborating effectively in a team
Key Responsibilities
- Support site management in compliance with SOPs, ICH-GCP, and protocols
- Assist with site initiation, routine monitoring, and close-out visits
- Perform source data verification (SDV) and support query resolution
- Maintain essential trial documentation in eTMF and sponsor systems
- Track investigational product (IP) accountability
- Collaborate with teams and escalate issues to ensure quality and timelines
Benefits/Perks
- Structured career development with mentoring and clear progression pathways
- Hands-on exposure to global trials across diverse therapeutic areas
- Formal training programs and continuous learning opportunities
- Flexible remote work model with competitive benefits
- Collaborative culture focused on quality, innovation, and well-being
- Global presence offering broad professional exposure
How to Apply
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Fortrea career page.
🔗 Click below to apply directly for this job
Interested candidates can apply directly through Fortrea’s official careers portal. Search for requisition ID 262254 on the Fortrea careers site. For more pharmaceutical careers and pharma jobs across India and globally, visit Pharma Recruiter.
Apply now to join a leading CRO and take the next step in your clinical research journey!
Why You Should Join
Fortrea fosters a supportive, innovative environment where early-career professionals thrive. You’ll gain valuable hands-on experience in a compliant, high-quality setting while benefiting from mentoring, global exposure, and long-term career stability in the dynamic pharmaceutical industry. Join a company recognized for raising CRO standards and driving meaningful impact in drug development.
FAQs
Q1: What experience is required for the CRA role at Fortrea?
A: This position suits candidates with 0–1 year of experience, including internships or up to 12 months of onsite monitoring.
Q2: Is German language proficiency mandatory?
A: Yes, fluency in both German and English (written and spoken) is required.
Q3: What is the work model for this position?
A: The role is primarily remote with travel required for site monitoring visits.
Q4: How can I grow my career as a CRA at Fortrea?
A: Benefit from structured training, mentoring, and exposure to multiple therapeutic areas with clear development pathways in a global CRO.
