Clinical Trial Scientist

Location Basel
Discipline: Clinical Development
Job type: Contract
Salary: £CHF 65.25 – CHF 77.96
Contact name: Harry Henson

Contact email: harry.henson@rbwconsulting.com
Contact phone: +44 (0)1293 364 092
Job ref: 2025-VIA-CTS
Published: 23 days ago
Duration: 12 months
Expiry date: 02 May 2025 10:59
Startdate: ASAP

​RBW Consulting are partnered with one of Switzerland's leading Pharma organisations in their search for a Clinical Trial Scientist to work on a contract basis.

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Start date - ASAP

Duration - 12 months at 1 FTE

Rate - CHF 65.25 –  CHF 77.96

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Summary

All tasks are performed in compliance with GCP and client SOPs. Depending on level of experience, the CTS may contribute to the following trial-level activities in collaboration with a more experienced trial scientist or may drive and accomplish some or all of the activities independently (Sr. CTS).

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Responsibilities

  • Member of the Clinical Trial Physician Team (CTP)

  • Collaborates closely with the Clinical Trial Physician (CTP) on relevant trial related activities

  • Develops a sound understanding of the science and medicine related to an indication and trial

  • Performs literature searches as needed to keep knowledge up to date.

  • Deliverables include the clinical trial protocol and related documents such as the ICF, study committee charters, study guidelines/instructions, PD code list, subject narratives, and the CSR.

  • Provides input into and reviews cross-functional trial documents such as the SAP, ESP requirements and specifications, monitoring guidelines, data review manual.

  • Performs data review and medical monitoring during the conduct of the trial.

  • Provides scientific input into responses for IRBs/ECs and HAs.

  • Participates in discussions with external experts.

  • Trains the relevant functions and roles on the scientific aspects of the trial.

  • Contributes to cross-functional and clinical development initiatives and processes as needed.

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Qualifications

  • PhD, Pharm D, MSc or equivalent university degree in life or health sciences.

  • At least 2-5 years of working experience preferably in clinical development in a contract research organization (CRO) or pharmaceutical company.

  • Previous experience in either the planning, set-up, conduct, closing, and reporting of phase II and III, experience in set-up and conduct, closing as an asset.

  • Clinical studies from a scientific perspective is an asset.

  • Fluent in English (written and oral).

  • Good understanding of the drug development process, trial-related regulatory requirements/ICH GCP guideline.

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