Clinical Research Jobs at IQVIA Germany
Looking to take the next step in Clinical Research Jobs with a global leader? IQVIA Biotech is hiring a Clinical Research Associate (CRA 2) in Germany, offering a home-based role with exceptional career development. This opportunity is ideal for professionals and job opportunities for life science students seeking long-term growth, exposure to diverse therapeutic areas, and a stable career in clinical research.
About IQVIA
IQVIA is a global leader in clinical research, data analytics, and technology solutions for the life sciences industry. Operating in over 100 countries, IQVIA supports innovation in healthcare by accelerating the development and commercialization of life-saving therapies. Through its strong commitment to professional development, IQVIA remains a top destination for Clinical Research Jobs worldwide.
Job Details:
- Job Title: Clinical Research Associate II (CRA 2) – IQVIA Biotech (m/w/d)
- Location: Home-based, Germany (Frankfurt/Main reference)
- Employment Type: Full-time, Permanent
- Job ID: R1519188
About the Role
IQVIA Biotech is seeking a Clinical Research Associate II (CRA 2) to join its growing team in Germany. This is a home-based role, offering the stability and global reach of a leading Contract Research Organization (CRO) combined with direct exposure to innovative biotech clients. This position is ideal for CRAs looking to deepen their monitoring expertise, expand into diverse therapeutic areas, and benefit from structured career development, mentoring, and world-class training.
Key Responsibilities in Clinical Research Job
- Perform site selection, initiation, monitoring, and close-out visits
- Support the development and execution of subject recruitment plans
- Evaluate site practices for quality and compliance with:
- Good Clinical Practice (GCP)
- International Council for Harmonisation (ICH) guidelines
- Track and manage study progress, including:
- Regulatory submissions
- Patient recruitment
- Case Report Form (CRF) completion
- Data query resolution
- Collaborate closely with:
- Investigative site staff
- Client representatives
- Internal cross-functional teams
- Participate in remote monitoring, study start-up activities, or therapeutic-area specialization, depending on the client model
- Mentor junior team members and act as a subject matter expert when required
Qualification Required:
- University degree in Life Sciences or another scientific discipline, or completed a healthcare apprenticeship
- 2–4 years of on-site monitoring experience, or equivalent combination of education and experience
- Strong knowledge of:
- GCP
- ICH guidelines
- Clinical research regulatory requirements
- Excellent written and verbal communication skills
- High attention to detail and ability to work in a fast-paced environment
- Fluent German (minimum C1 level) and good command of English
- Willingness to travel 40–60%
- Valid Class B driver’s license
What IQVIA Offers in Clinical Research Jobs
- Permanent employment contract
- Home office with flexible working hours
- Company car and accident insurance
- Access to extensive training, mentoring, and career development resources
- Exposure to a wide range of biotech, pharmaceutical, and medical device studies
Application Process
Please submit:
- CV (in English)
- Motivation letter
- Education certificates
- Job reference letters (Arbeitszeugnisse)
Why IQVIA Biotech?Â
At IQVIA Biotech, your career growth is intentional. Whether your goal is therapeutic specialization, leadership, or broader clinical development exposure, IQVIA provides the resources and support to help you get there.
