Clinical Research Associate

vor 2 Wochen


Frankfurt am Main, Hessen, Deutschland IQVIA Vollzeit

About the Role


IQVIA is seeking an experienced Clinical Research Associate to join our team in Germany. As a CRA, you will be responsible for conducting site selection, initiation, monitoring, and close-out visits.



Job Description:

The ideal candidate will have a university degree in life science or other scientific discipline, and minimum one year of on-site monitoring experience.



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.
  • Minimum of one year of on-site monitoring 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.


About You:

  • You have excellent analytical and problem-solving skills.
  • You are able to communicate complex information clearly and concisely.
  • You have a strong understanding of clinical trials and their management.


What We Offer:

  • A competitive salary of €70,000 per annum.
  • A comprehensive benefits package including home-office, company car/car allowance, accident insurance, pension, and more.


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