CH - Scientist 2, Clinical Research / Clinical Scientist

☞ Randstad Switzerland

View: 121

Update day: 25-04-2024

Location: Basel Basel-Stadt BS

Category: R & D IT - Software

Industry: Staffing Recruiting

Position: Associate

Job type: Full-time

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Job content

Do you want to work in a big pharmaceutical company? Do you have experience with Clinical Trial? You should then read the following lines!Our client, based in Basel, is looking for a Clinical Scientist for a 7 months contract.The focus of this position is to plan, design, scientifically monitor and report clinical studies. The incumbent is responsible for the compliance of the assigned clinical study(ies) with department, company and regulatory standards and procedures.The incumbent will support the Pulmonary Hypertension TA.Your Responsabilities
  • Is responsible for delivering the clinical study protocol and contributes to the development of other clinical study documents, e.g. Informed Consent Form, Case Report Form, etc.
  • Plans, manages and monitors daily activities of clinical studies which require scientific input, e.g. contribution to answers to trial-related Health Authorities’ (HA) questions, answer to Ethic Committees /Institutional Review Boards questions, etc.
  • Performs medical monitoring/ reporting including evaluation of adverse events.
  • Reviews, evaluates and reports results of clinical studies.
  • Manages study-related committees, external medical experts etc.
  • Ensures that all activities are in compliance with department, company and regulatory standards and procedures.
  • As requested, contributes to the development and execution of clinical research programs for assigned company products, e.g. Clinical Development Plans, Clinical Overviews, HAs’ Briefing Books, HAs’ Annual Reports, Pediatric Investigational Plans, etc.
  • As requested, participates on cross functional teams, e.g. improvement of processes, etc.
Your Profile
  • PhD, PharmD, DVM, MSc (or equivalent) degree in Biological Sciences required.
  • At least 5 years experience in Clinical Development, and hands on experience on conducting clinical trials.
  • Knowledge of clinical development processes, clinical trial processes, and regulatory requirements/ ICH guidelines based on previous deliverables.
  • Prior experience of working in a matrix organization including interactions with all relevant functions involved in a clinical trial and program (e.g. Biostatistics, Data Management, Operations, Regulatory, Drug Safety, external service providers, etc.).
  • Good leadership skills.
  • Demonstrated analytical skills.
  • Excellent computer systems and software skills.
  • Excellent English, other languages advantageous.
Do not waste any minutes, apply now! We are looking forward to receiving your application.Please note that only candidates with a valid work permit or who are EU/EFTA citizens will be considered.
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Deadline: 09-06-2024

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