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: | 1 day 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.
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!
Latest jobs
- Clinical Trial Scientist
-
Job location: Basel Job salary: £CHF 65.25 – CHF 77.96
RBW Consulting are partnered with one of Switz...
- Clinical Trial Physician
-
Job location: Basel-Landschaft Job salary: £CHF 86.44 – CHF 90.67
RBW Consulting are partnered with one of Switze...
- Associate QA Manager
-
Job location: Stoke-on-Trent Job salary: £Competitive
Associate QA ManagerAre you an experienced Sen...