Senior Clinical Scientist

May 27, 2024

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Senior Clinical Scientist

Contracting

Ref: BH-1995-1

Senior Clinical Scientist

Job details

Contracting

Ref: BH-1995-1

Website headcount

Senior Clinical Scientist 

Location: Basel (hybrid).
Start: ASAP
Duration: 6 months
Workload: 100%

Our client, a Swiss Pharmaceutical company specializing in innovative medicines for rare diseases, is in the process of launching their first commercial product. They are seeking a Clinical Scientist to provide scientific and medical expertise to various products across various stages of clinical development to facilitate regulatory submissions.

Your tasks:

  • Develop a thorough understanding of scientific and medical aspects to prepare key documents (e.g., Investigator Brochures, regulatory submission documents, presentations).
  • Write, review, amend, and facilitate cross-functional processes for protocol preparation.
  • Provide insights, review cross-functional trial materials, and oversee data review and medical oversight.
  • Oversee study planning adequacy and direct clinical program implementation.
  • Manage project budgets, prioritize timelines, and ensure adequate staffing.
  • Participate in ongoing data review processes and present at investigator meetings.
  • Engage in ad hoc discussions, contribute to document standardization and procedural refinement.
  • Participate in corporate committees and assist in special projects as needed.
  • Contribute to cross-functional and clinical development initiatives and processes as required.

Your profile:

  • PhD, Pharm D, MSc, or equivalent degree in life or health sciences.
  • Minimum of 2 years’ experience in medical or technical writing. 
  • Immunology experience is highly valuable.
  • Clinical monitoring experience is preferred.
  • Strong medical/scientific and clinical research knowledge.
  • Familiarity with clinical trial design, basic statistics, pharmacodynamics, and pharmacokinetics.
  • Proficient in data interpretation.
  • Experience in protocol development, study report preparation, Investigator Brochure preparation, and regulatory submissions.
  • Comprehensive understanding of the drug development process.
  • Knowledge of GCP and ICH Guidelines.

Please apply directly online with your CV.

**Please only apply if you are eligible to work in Switzerland and the EU**

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