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Clinical Research Associate II

Clinical Research Associate II

LocationAmsterdam, Netherlands
Business SectorBiotechnology
Contact email
Job ref23592
Published3 months ago
Clinical Research Associate II

Are you an experienced CRA, or just starting out in the field? If so, we are looking for you! If you are currently working as a CRA and are open to a new challenge, this is the role for you.

Our partner, a dynamic CRO based in the Amsterdam area, is seeking an experienced, Dutch-speaking CRA. This organization is a leading provider of healthcare information and clinical research.

At this company, career progression is more of a rule than an exception. In fact, junior management positions are almost never filled externally, as these roles are reserved for CRAs who grow within the company.

Responsibilities:
  • Manage investigator sites and monitoring activities for assigned clinical studies successfully.
  • Be involved in the entire trial life cycle, from start-up to close-out.
  • Gain exposure to a wide range of therapeutic areas.
  • Enjoy a high degree of flexibility in scheduling your hours, with the option to work fully from home.

Profile:
  • Willingness to travel.
  • At least one year of experience in monitoring clinical studies at a CRO or pharmaceutical company.
  • Strong knowledge of clinical research process, including working knowledge of all functional areas of clinical trials and medical terminology.
  • Experience in monitoring and/or coordinating clinical trials required.
  • Excellent written and verbal communication skills to express complex ideas to study personnel at research and clinical institutions.
  • Able to form productive professional relationships both internally within own function, cross-functionally and externally with health care professionals.
  • Able to handle several priorities within multiple, complex trials.
  • Able to reason independently and recommend specific solutions in clinical settings.
  • Able to work independently, prioritize, and work within a matrix team environment.
  • Knowledge of current GCP/ICH guidelines applicable to the conduct of clinical research.
  • Fluent in Dutch and English at a professional level.

Interested?
Contact Khanyi Mabena for more information by calling +31 2020 44502 or emailing k.mabena@panda-int.com.