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.
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 4 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
* Previous experience in the Therapeutic area of Cardiovascular, Renal and/or Central Nervous System Diseases is an advantage
* Good knowledge of drug development and clinical trial process
* Good knowledge of regulatory requirements/ICH guidelines
* Demonstrated ability to work independently in a fast-paced environment, to prioritize multiple competing tasks, to proactively address issues and demands
* 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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