Clinical Trial Scientist

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.

Start date - ASAP

Duration - 12 months at 1 FTE

Rate - CHF 65.25 - CHF 77.96

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).

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.

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.

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