Senior Clinical Trial Scientist

☞ PharmiWeb.Jobs

View: 203

Update day: 20-03-2024

Location: Allschwil Basel-Landschaft BL

Category: R & D IT - Software

Industry: Research Biotechnology Pharmaceuticals

Position: Associate

Job type: Contract

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Job content

A current vacancy as a Senior Clinical Trial Scientist with a leading pharmaceutical company is available in Switzerland.

Our client is looking for candidates based in Switzerland / EU passport holder for an initial 12-month full time contract.

The successful candidate will be a core member of the clinical trial team.

Job Responsibilities
  • Collaborates closely with the Clinical Trial Physician on relevant trial-related activities
  • Develops a sound understanding of the science and medicine related to an indication and trial
  • Main deliverables include the clinical trial protocol and related documents such as the ICF, study committee charters, study guidelines/instructions, PD code list, subject narratives, and the CSR
  • Provides input into and reviews cross-functional trial documents such as the SAP, ESP 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 and HAs
  • Participates in discussions with external experts
  • Trains the relevant functions and roles on the scientific aspects of the trial
  • Contributes to cross-functional and clinical development initiatives and processes as needed
Key Experience And Requirements
  • PhD, Pharm D, MSc or equivalent university degree in life or health sciences
  • At least 5 years of working experience in clinical development, in a contract research organization (CRO) or pharmaceutical company
  • Experience in writing clinical study protocols
  • Experience/Knowledge in the filed of kidney diseases and/or autoimmune diseases is desirable
  • Previous experience in either the planning, set-up, conduct, closing, and reporting of phase II and III clinical studies from a scientific perspective
  • Results driven attitude and good sense of urgency
  • Able to anticipate and proactively address issues and demands
  • Effectively negotiates with key stakeholders to influence, convince, and gain their buy-in and agreement
  • Thinks globally and has an appreciation and understanding of the big picture (e.g., competitor activities, potential implications and consequences of own activities and decisions)
  • Able to travel occasionally as required to fulfil responsibilities and tasks
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Deadline: 04-05-2024

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