Job Details

Clinical Project Scientist

4881
  • ₣Competitive
  • Basel , Switzerland
  • Contract
Clinical Project Scientist

Location: Switzerland
Start Date: ASAP
Market Leading Rate

One of the world's leading pharmaceutical companies is seeking an enthusiastic experienced Clinical Project Scientist to become an integral member within their Clinical Science team. Working in close collaboration with the clinical trial physician, in this role you will design and execute clinical plans and trials across multiple diseases and indications. With state-of-the-art facilities, a commitment to cutting-edge research, and a vibrant multicultural community, this company offers an inspiring and supportive place to advance your career.

What will you be doing?
  • You will collaborate closely with the Clinical Trial Physician on all relevant trial activities and in representing the trial/program at internal and external meetings.
  • Use your expertise to provide scientific input into trial level documents such as protocols and related documents, IBs, briefing books for health authority meetings, clinical overviews and summaries.
  • Host meetings with external clinical experts and contribute to scientific discussions.
  • Perform literature reviews and acquire medical and scientific knowledge relevant to the project requirements.
  • Provide scientific input to trial-related data review and medical monitoring activities.
  • Build and strengthen relationships with internal and external stakeholders.
  • Manage communication with the relevant Health Authorities.
  • Help drive excellence in the Clinical Science Team, offering innovative solutions to any challenges and issues that arise.
  • Matrix team management.

What do you bring to the table?
  • Extensive pharmaceutical industry clinical trial experience (10+ years).
  • Graduate degree in a life sciences subject (MSc/PhD preferred).
  • Demonstrable experience across all phases of clinical trials (preclinical through to phase III).
  • Advanced knowledge of several therapeutic areas (preference for rare/orphan diseases).
  • Expert of drug development, clinical trial processes, and regulatory requirements.
  • English (fluent), and German or French (desired).
Robyn O'Toole Recruitment Consultant

Apply for this role

© Warman O'Brien 2023
Site by Venn