Clinical Trial Scientist

Vor 2 Tagen


Basel, Basel-Stadt, Schweiz Actalent Vollzeit

I am representing our client in the Basel area, who is looking for a Clinical Trial Scientist to join their dynamic team. This role involves collaborating closely with the Clinical Project Scientist on trial-related activities, developing a deep understanding of the science and medicine related to the trial, and contributing to various cross-functional and clinical development initiatives. The ideal candidate will have a strong background in life or health sciences, significant experience in clinical development, and a proven ability to work independently in a fast-paced environment.

Job Responsibilities

  • Collaborates closely with the Clinical Project Scientist on relevant trial-related activities
  • Develops a sound understanding of the science and medicine related to an indication and trial and performs literature searches as needed to keep knowledge up to date
  • Main deliverables include the clinical trial protocol and related documents such as the ICF, trial committee charters, trial guidelines/instructions, PD code list, participant narratives, and the CSR
  • Provides input into and reviews cross-functional trial documents such as the SAP, external service provider requirements and specifications, monitoring guidelines, data review manual
  • Performs data review and medical monitoring during the conduct of the trial
  • Coordinates/manages the study committees
  • Provides scientific input into responses for IRBs/ECs, HAs, sites and monitors

Candidate Requirements

  • PhD, Pharm D, MSc or equivalent university degree in life or health sciences
  • At least 4 years of working experience preferably in clinical development in a contract research organization (CRO) or pharmaceutical company. Monitoring experience is an advantage
  • Experience in the planning, set-up, conduct, closing, and reporting of phase II and III clinical studies from a scientific and operational perspective
  • Previous authoring/co-authoring of clinical trial protocols, ICFs, scientific trial-related documents (e.g., trial committee charters) is an advantage
  • Previous experience in the Therapeutic area of Cardiovascular, Renal and/or Central Nervous System Diseases is an advantage
  • Fluent in written and spoken English
Seniority level

Mid-Senior level

Employment type

Full-time

Job function

Science

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