Clinical Project Scientist

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View: 158

Update day: 25-04-2024

Location: Allschwil Basel-Landschaft BL

Category: R & D IT - Software

Industry: Staffing Recruiting

Position: Associate

Job type: Full-time

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Job content

The Life Science Career Network

CTC are specialised industry experts who can help companies source the best talent and provide reliable HR and consulting services, support varied candidates in finding promising career opportunities and offer the latest in skill development training programmes.

Clinical Project Scientist

Our client, an innovative and dynamic bio-pharmaceutical company headquartered in Switzerland, covering multiple therapeutic areas, is looking a Clinical Project Scientist for permanent role based in Basel, Switzerland.

Responsibilities
  • Provide scientific input into relevant documents such as the Clinical Development Plans, Communication Plans, Investigators Brochures, clinical overviews and summaries, etc.;
  • Collaborate closely on relevant projects activities with the Clinical Project Physician and jointly represent the project during internal and external meetings;
  • Provide scientific input to medical monitoring activities on project level;
  • Gain an expert understanding of the scientific and medical elements of clinical trials, including understanding the competitive landscape, contributes as needed to trial-level activities and provide mentorship and training to junior colleagues;
  • Participate in meetings with health authorities as well as in life cycle activities and life cycle meetings.
Qualifications And Experience
  • Swiss working/residency permit and/or Swiss/EU-Citizenship required;
  • PhD, Pharm D, MSc or equivalent university degree in Neurology, Neuroscience, or disciplines related to Neuroscience, CNS or Insomnia;
  • At least 3 years of working experience as a Clinical Scientist, working on Phase II and III clinical studies within a CRO, biotech and/or pharma company;
  • Experience in independently writing clinical study protocols, ICFs, scientific trial-related documents e.g., study committee charters;
  • Solid experience in planning, set-up, conduct, closing, and reporting of phase II and III clinical studies from a scientific perspective;
  • Previous scientific contribution to cross-functional trial documents (e.g., SAP) guidelines, CRFs;
  • Solid experience with data review/medical monitoring;
  • Good understanding of the drug development process, trial-related regulatory requirements/ICH GCP guidelines.
Would you like to learn more about CTC and the opportunity outlined? Please, get in contact with us: you may either use the ’apply now’ button, or write an email to us, or reach out to us on the phone.
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Deadline: 09-06-2024

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