Clinical Trial Physician (Cardiovascular)

  • Salary: 77.96 CHF p/h
  • REF Number: v-51651
  • Consultant: Karen Kangley
  • Contact: 01246 457733
  • Date Published: 25.03.2024
  • Closed Date: 08.04.2024
  • Industry: Pharmaceutical
  • Location: Switzerland, Switzerland
  • Functional Expertise: Clinical Operations/Development

CK Group are recruiting for a Clinical Trial Physician to join a Swiss high-potential biopharmaceutical company, specialized in the discovery, development and commercialization of innovative small molecules, with the aim of transforming the horizon of therapeutic options. The Clinical Trial Physician will play a key role in a large global phase 3 cardiovascular outcome study.

The position will be for a 12-month contract, located near at the clients office near Basel, the rate for this role will be 77.96 CHF per hour.

Job Responsibilities:

  • Provide medical leadership internally for the trial activities assigned, through a comprehensive understanding of the science, medicine, product environment and competitive landscape relating to a disease area.
  • Contribute to the core medical/scientific information required in all clinical documents of the respective trial (e.g. protocols, core informed consent forms, clinical study reports, safety related documents etc.).
  • Work with the Clinical Lead by contributing to global strategic development.
  • Writing protocol amendments and other study related documents such as the Informed Consent Form (ICF), committee(s) charter(s), subject narratives and the Clinical Study Report (CSR).
  • Performing literature reviews and write position papers as necessary.
  • Working alongside the Cardiovascular Medical Expert.

Candidate’s Requirements:

  • MD
  • At least 2 years’ experience in clinical research in a Pharmaceutical and/or Biotech company or equivalent in Academia preferably within cardiovascular therapeutic area.
  • Experience in patient education is a plus.
  • Good knowledge of drug development and clinical trial process based on previous experience.
  • Good knowledge of regulatory requirements/ICH guidelines.
  • Good organizational and communication skills, able to work as part of a team and independently.
  • Proven record of successfully engaging and interacting within a complex and challenging matrix organization as well as with all levels of seniority.
  • Results driven attitude and good sense of urgency.
  • Able to anticipate and proactively address issues and demands, solution oriented and hands-on.
  • Analytical thinking, data and detail oriented.
  • Shares knowledge and expertise openly.
  • Excellent written and spoken communication skills in English.
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Right to work in Switzerland is essential for this position. Please quote job reference T56780 in all correspondence.

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