Senior Clinical Trial Scientist - Basel - 12 month contract
Location | Basel-Landschaft |
Discipline: | Clinical Development |
Job type: | Contract |
Salary: | £CHF 65.25 - CHF 73.72 |
Contact name: | Harry Henson |
Contact email: | harry.henson@rbwconsulting.com |
Contact phone: | +44 (0)1293 364 092 |
Job ref: | 33328 |
Published: | 3 months ago |
Duration: | 12 months |
Expiry date: | 22 Aug 2024 11:59 |
Startdate: | ASAP |
RBW Consulting are proud to be partnered with one of the worlds leading Biotech's in their search for multiple Senior Clinical Trial Scientists to be based out of Basel for a 12 month contract starting ASAP!
Job Responsibilities
The Senior Clinical Trial Scientist is representing clinical science as core member of the Clinical Trial Team and contributes to the following trial-level activities:
Collaborates closely with the Clinical Trial Physician, Clinical Project Physician and/or Clinical Project Scientist 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
Candidate Requirements
PhD, Pharm D, MSc or equivalent university degree in life or health sciences
At least 5 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
Please apply here and Harry Henson will be in touch to discuss your application further.