Clinical Trial Physician

Location Basel-Landschaft
Discipline: Clinical Development
Job type: Contract
Salary: £CHF 86.44 – CHF 90.67
Contact name: Harry Henson

Contact email: harry.henson@rbwconsulting.com
Contact phone: +44 (0)1293 364 092
Job ref: 2025-VIA-CTP
Published: 1 day ago
Duration: 12 months
Expiry date: 02 May 2025 10:59
Startdate: ASAP

RBW Consulting are partnered with one of Switzerland's leading ​Pharmaceutical companies in their search for a Clinical Trial Physician to join them on a contract basis.

​

Start date - ASAP

Duration - 12 months at 1 FTE

Rate - CHF 86.44 – CHF 90.67 per hour

​

Summary
All tasks below should be performed in compliance with Good Clinical Practices and client SOP’s. The CTP is a member of the Clinical Trial Team (CTT). The tasks and activities of the CTP are carried out in close collaboration with the Clinical Trial Scientist (CTS) for the trial related activities and with the Clinical Project Physician (CPP) and Clinical Project Scientist (CPS) for the project related activities.

Key Responsibilities

  • Develop a sound understanding of the science and medicine relating to a therapeutic area.

  • Develop a sound understanding of the complexity of global clinical development with a particular attention to methodological and ethical aspects of development, in the assigned therapeutic area.

  • Contribute to writing of the clinical trial Protocol including amendments and related documents such as the Informed Consent Form (ICF), committee(s) charter(s), subject narratives and the Clinical Study Report (CSR).

  • Deliver medical training to the Clinical Trial Team (CTT) members and/or staff.

  • Deliver medical oversight of the study (including safety, medical review of data during the trial, quality and performance of the trial).

  • Interpret Clinical Trial data.

  • Interact with external Experts, Steering Committees (SC), Independent Data Monitoring Committees (IDMC), other study or project committees.

  • Answer to trial-related EC/IRB and HA questions

Qualifications & experience

  • MD.

  • At least 4 year experience in clinical research in a Pharmaceutical or Biotech company or equivalent in Academia.

  • Clinical research or Clinical experience in the indication relevant to the Clinical Project is preferred.

  • Good knowledge of drug development and clinical trial process based on previous experience.

  • Good knowledge of regulatory requirements/ICH guidelines.

  • Good organizational skills, able to work as part of a team and independently.

  • Good communication skills.

  • Detailed oriented.

  • Fluent in English (written and oral).

​

Please apply here and Harry Henson will be in touch to discuss your application further.