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Clinical Research Associate 2 or Senior Clinical Research Associate 1 (m/w/d), Single Sponsor
Zusammenfassung
A leading global clinical research organization is seeking a Clinical Research Associate 2 to monitor clinical trials throughout Germany. The role includes site selection, adherence to regulatory standards, and supporting subject recruitment. Ideal candidates should have a degree in life sciences, 2-4 years of monitoring experience, strong communication skills, and be fluent in German. This position also offers benefits like flexible work schedules and career growth resources.
Leistungen
Qualifikationen
- Minimum of two to four years of on-site monitoring experience or equivalent.
- Flexibility to travel up to 40-60% of working time.
- Driver’s license class B required.
Aufgaben
- Perform site selection, initiation, monitoring and close-out visits.
- Support development of subject recruitment plan.
- Evaluate quality of site practices per regulatory standards.
Kenntnisse
Ausbildung
Join IQVIA as a Clinical Research Associate 2 (CRA 2) or as Senior Clinical Research Associate 1 (SrCRA 1) (m/w/d) and work home-based throughout Germany in our single sponsor department.
You will enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our clients.
Whether you're just starting out or looking to deepen your expertise, this role promises to offer intentional career growth and professional development. With access to world-class training and mentoring, you’ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.
- Performing site selection, initiation, monitoring and close-out visits
- Supporting the development of a subject recruitment plan
- Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
- Collaborating with experts at study sites and with client representatives
- Depending on client model there might be remote-monitoring, involvement in study start-up processes, specialization on therapeutic area (pharmaceutical product or medical devices)
- Mentoring of less experienced team members, support as subject matter expert for specific topics or additional tasks might be included
- University Degree in life science or other scientific discipline or apprenticeship in the health care field
- Minimum of two to four years of on-site monitoring experience, or an equivalent combination of education, training and experience
- Knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Strong written and verbal communication skills, attention to detail and ability to work in a fast-paced environment
- Fluency in German at C1 level and a good command of English
- Flexibility to travel up to 40-60% of working time
- Driver’s license class B
- Resources that promote your career growth
- Leaders that support flexible work schedules
- Programs to help you build your therapeutic knowledge
- Dynamic work environments that expose you to new experiences
- Home-office, company car, accident insurance and more
Whatever your career goals, we are here to ensure you get there!
Please apply with your English CV and motivation letter.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
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