- 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.
- Might include supporting early phase / phase I clinical trials.
- University Degree in life science or other scientific discipline or apprenticeship in health care .
- Minimum of one year of on-site monitoring experience , alternatively 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 pace environment.
- Fluent language skills in German on at least C1 level and a good command of English .
- Flexibility to frequent business travel.
- 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 or car allowance, accident insurance and more.
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Clinical Research Associate or Senior CRA - Frankfurt, Deutschland - IQVIA
Beschreibung
We are looking for an experienced CRA or Senior CRA (m/w/d) for a sponsor dedicated role in cooperation with Boehringer Ingelheim , one of the largest and most established pharmaceutical companies in Germany (family owned since 1885), with focus on therapeutic areas such as Pulmonology, Oncology and Neurology.
When you join the IQVIA sponsor-dedicated cFSP team home-based throughout Germany , you'll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with our client. Whether you're just starting out or looking to deepen your expertise, this role promises to offer intentional career growth and professional development.
Your responsibilities will include:
Qualifications:
What you can expect:
Whatever your career goals, we are here to ensure you get there
We invite you to join IQVIA.
Please apply with your English CV, motivation letter and your certificates and reference letters.
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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
