Experienced Clinical Research Associate
Vor 7 Tagen
Join IQVIA as a CRA II / SrCRA (m/w/d) in our Clinical Site Management department home-based throughout Germany. You will focus on a comprehensive clinical trial management in a variety of indications and learn about the diverse scientific approach of the sponsors. Beside establishing strong relationships with the global study team and the involved investigators, you will conduct monitoring on complex clinical trials for different pharma companies and assure their adherence to good clinical practices and study protocols.With strategic site relationship managers supporting you throughout your role, this is a fantastic opportunity for you to embed yourself in the wider clinical operations team and work on ground-breaking new medicine development.Your responsibilities will include: 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 on study sites and client representatives.Qualifications: University Degree in life science or other scientific discipline or apprenticeship in health care.Minimum of two years of on-site monitoring experienceKnowledge 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.Good command of German and English.Flexibility to business travel up to 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/car allowance, accident insurance, pension and more.Whatever your career goals, we are here to ensure you get therePlease 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
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Senior Clinical Research Associate
vor 2 Wochen
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Experienced Clinical Trial Coordinator
Vor 6 Tagen
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Experienced Clinical Trial Coordinator
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Frankfurt, Deutschland IQVIA VollzeitJoin 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...
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vor 2 Wochen
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vor 2 Wochen
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vor 10 Stunden
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Vor 7 Tagen
Frankfurt am Main, Deutschland ICON Plc VollzeitCRA, germany, sponsor dedicated ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Clinical Research Associate II to join...
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vor 2 Wochen
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Experienced Clinical Trial Coordinator
Vor 5 Tagen
Frankfurt, Deutschland IQVIA VollzeitThe IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to work with the preparation and documentation of clinical research projects in different therapeutic areas. You will be involved in data...