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Frankfurt am Main, Hessen, Deutschland IQVIA VollzeitJoin IQVIA asTraineeClinical Research Associate/ Associate CRA(m/w/d) in the sponsor dedicated teamand work inhome-office in East or South Germany.In ourClinical Functional Service Partnershipmodels, we work in a close partnership with key customers to deliver a comprehensive clinical trial management. Within this team, you will focus on different projects...
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Frankfurt am Main, Hessen, Deutschland IQVIA VollzeitJoin IQVIA as aClinical Research Associate 2/ CRA 2or asSenior Clinical Research Associate1/SrCRA 1(m/w/d) and workhome-based throughout Germanyin oursingle 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...
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Trainee Clinical Research Associate
vor 2 Wochen
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Clinical Research Associate
vor 3 Wochen
When you join IQVIA as a sponsor-dedicated Clinical Research Associate / CRA (m/w/d) home-based throughout Germany, you’ll 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.
Your responsibilities will include:
- Performing site selection, initiation, monitoring and close-out visits
- 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)
Qualifications:
- University Degree in life science or other scientific discipline or apprenticeship in the health care field
- Minimum of one year of on-site monitoring 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 pace environment
- Fluency in German on at least C1 level and a good command of English
- Flexibility to travel up to 40-60% of working time
- Driver’s license class B
What you can expect:
- 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
We invite you to join IQVIA.
LI-KA1
CRASDAJD
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at
