The Life Science Career Network
CTC are specialised industry experts who can help companies source the best talent and provide reliable HR and consulting services, support varied candidates in finding promising career opportunities and offer the latest in skill development training programmes.
Our client, an innovative Swiss bio-pharmaceutical company focused on discovering, developing, and commercializing small molecules to address unmet medical needs, is seeking a Clinical Trial Scientist for a 12-month contract in the Basel area, with potential for extension .
Main Responsibilities:
Collaborates closely with the Clinical Project Scientist or Clinical Trial Physician on relevant trial-related activities
Develops a sound understanding of the science and medicine related to an indication and trial and performs literature searches as needed to keep knowledge up to date
Main deliverables include the clinical trial protocol and related documents such as the ICF, trial committee charters, trial guidelines/instructions, PD code list, participant narratives, and the CSR
Provides input into and reviews cross-functional trial documents such as the SAP, external service provider requirements and specifications, monitoring guidelines, data review manual
Performs data review and medical monitoring during the conduct of the trial
Coordinates/manages the study committees
Provides scientific input into responses for IRBs/ECs, HAs, sites and monitors
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 and Experience:
Relevant Swiss working/residency permit and/or Swiss/EU-Citizenship required.
PhD, Pharm D, MSc or equivalent university degree in life or health sciences
At least 2 years of working experience preferably in clinical development in a contract research organization (CRO) or pharmaceutical company. Monitoring experience is an advantage
Experience in the planning, set-up, conduct, closing, and reporting of phase II and III clinical studies from a scientific and operational perspective
Previous authoring/co-authoring of clinical trial protocols, ICFs, scientific trial-related documents (e.g., trial committee charters) is an advantage
Good understanding of cross-functional clinical trial team roles, responsibilities, processes, and
deliverables.
Fluent in written and spoken English
If you'd like to learn more about CTC and the outlined opportunity, please contact us using the 'apply now' button or by emailing vanessa.gilardoni@ctcresourcing.com.
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