Clinical Research Associate

vor 1 Woche

Frankfurt am Main, Hessen, Deutschland IQVIA Vollzeit
Job Title: Experienced Clinical Research Associate

IQVIA is seeking an experienced Clinical Research Associate to join our Clinical Site Management department in Germany. As a key member of our team, you will be responsible for conducting monitoring visits on complex clinical trials for various pharmaceutical companies, ensuring adherence to good clinical practices and study protocols.

Key Responsibilities:
  • Perform site selection, initiation, monitoring, and close-out visits.
  • Support the development of a subject recruitment plan.
  • Evaluate the quality and integrity of site practices in accordance with regulatory requirements.
  • Manage progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolution.
  • Collaborate with experts on study sites and client representatives.
Requirements:
  • University degree in life science or other scientific discipline or apprenticeship in healthcare.
  • 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.
  • Strong written and verbal communication skills, attention to detail, and ability to work in a fast-paced environment.
  • Good command of German and English.
  • Flexibility to business travel up to 60% of working time.
  • Driver's license class B.
What We Offer:
  • Resources that promote career growth.
  • Leaders that support flexible work schedules.
  • Programs to help build therapeutic knowledge.
  • Dynamic work environments that expose you to new experiences.
  • Home-office, company car/car allowance, accident insurance, pension, and more.

We invite you to join IQVIA and take advantage of our comprehensive benefits package and opportunities for career growth and development.

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