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Clinical / Medical Scientist

headcount | recruitment driven by science

On-site Contract 4d ago

About the role

About

We are supporting a pharma company in Basel that is looking for a Clinical / Medical Scientist to join their team on a 12 month contract. This role will focus on supporting clinical trial execution, medical monitoring, and cross-functional collaboration across ongoing clinical programs.

This position is ideal for someone with strong clinical development experience who enjoys working in a collaborative, outsourced CRO model and can contribute both scientifically and operationally.

Responsibilities

  • Draft key clinical trial and program-level documents in collaboration with Clinical Operations, Biostatistics, Medical Writing and CRO partners
  • Support clinical aspects of study startup, execution and close-out in close collaboration with Clinical Operations, Data Management and CROs
  • Contribute to medical monitoring of efficacy and safety data from clinical trials
  • Act as a point of contact for investigational sites to ensure smooth study conduct
  • Support the development and execution of the Data Review Plan
  • Contribute to the analysis and drafting of clinical trial reports and scientific publications
  • Support planning, conduct and follow-up of external clinical development and study-related meetings
  • Maintain clinical aspects of the Trial Master File
  • Provide operational support to the Clinical Development team including meeting coordination, inspection readiness and general organization

Requirements

  • Bachelor’s or advanced degree in a scientific discipline, or Medical Degree
  • 5+ years of experience in the pharmaceutical industry, including at least 3 years within Clinical Development teams
  • Experience managing clinical trials within multidisciplinary teams
  • Experience working in fully outsourced CRO models
  • Strong medical and scientific expertise relevant to clinical programs
  • Thorough knowledge of Good Clinical Practice, clinical trial design, statistics, regulatory processes and clinical development
  • Excellent scientific writing skills
  • Strong understanding of statistical analysis methods with the ability to interpret and communicate data clearly
  • In-depth knowledge of drug development processes

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