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Clinical Study Manager

vor 2 Wochen


Basel, Basel-Stadt, Schweiz Actalent Vollzeit

About the Job:

The ideal candidate will have solid knowledge and experience in clinical pharmacology science combined with hands-on expertise in quantitative-qualitative data analysis. You will be responsible for the overall planning, management, data evaluation, and reporting of clinical pharmacology studies as an individual contributor.

Your Responsibilities:

  • Clinical Studies: Plan, manage, and report on clinical pharmacology studies.
  • Capacity Extension: Identify solutions for clinical study support through internal groups and external relationships.
  • Data Visualization: Utilize advanced data visualization tools to facilitate data-driven decision-making.
  • Modeling: Understand and apply modeling techniques to support model-informed drug development (MIDD).
  • Regulatory Compliance: Ensure regulatory compliance by integrating regulatory requirements into clinical studies and project workflows.

What We Offer:

  • Competitive salary and benefits package.
  • Opportunities for professional growth and development.
  • Collaborative and dynamic work environment.