Senior Clinical Trial Scientist (7106)

CTC Resourcing Solutions; Basel; Vor Ort; CHF 150.000 - 190.000; Vollzeit

Zusammenfassung

CTC Resourcing Solutions is recruiting on behalf of a client for a Senior Clinical Trial Scientist on a 12-month contract based in the Basel area. The role demands in-depth scientific and medical understanding of indications and trials, with core deliverables including protocols and related documents.

The candidate will provide input into cross-functional trial documents, perform data review and medical monitoring, and contribute to regulatory responses and external expert discussions while

Qualifikationen

• Swiss work permit or citizenship required.
• PhD or equivalent in life/health sciences.
• Minimum 5 years in clinical development in CRO or pharmaceutical.
• Experience with Phase II–IV trials and monitoring.
• Experience authoring clinical study protocols, ICFs and related documents.
• Ability to coordinate cross-functional activities.
• Knowledge of drug development and regulatory requirements/ICH guidelines.
• Fluent in written and spoken English.

Aufgaben

• Develop understanding of science and medicine related to an indication and trial.
• Deliverables include the clinical trial protocol and related documents.
• Provide input into and review cross-functional trial documents (SAP, ESP requirements, specifications, monitoring guidelines, data review manual).
• Perform data review and medical monitoring during the conduct of the trial.
• Provide scientific input into responses for IRBs/ECs and HAs.
• Participate in discussions with external experts.
• Train relevant functions and roles on the scientific aspects of the trial.
• Contribute to cross-functional and clinical development initiatives and processes as needed.

Kenntnisse

Swiss permit / citizenship

5+ years experience

Phase II–IV trials

Study protocols & ICFs

Cross-functional teamwork

Drug development knowledge

Regulatory knowledge / ICH

Independent / fast-paced work

English fluency

Ausbildung

Life/Health sciences degree (PhD/PharmD/MSc)

Jobbeschreibung

CTC is a specialized search and recruitment partner for the Life Sciences industry, serving clients and candidates since 1997. We enable careers by connecting talented professionals with meaningful opportunities, and we support our clients in engaging, retaining, and developing the right talent when needed.

For one of our clients, we are currently recruiting for a:

Senior Clinical Trial Scientist

on a 12-month contract based in Basel area.

Main Responsibilities:

• Develop a sound understanding of the science and medicine related to an indication and trial.
• Main deliverables include the clinical trial protocol and related documents.
• Provide input into and review cross-functional trial documents such as the SAP, ESP requirements and specifications, monitoring guidelines, data review manual.
• Perform data review and medical monitoring during the conduct of the trial.
• Provide scientific input into responses for IRBs/ECs and HAs.
• Participate in discussions with external experts.
• Train the relevant functions and roles on the scientific aspects of the trial.
• Contribute 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 5 years of working experience, preferably in clinical development in a contract research organization (CRO) or pharmaceutical company.
• Good experience in planning, setting up, conducting, closing, and reporting phase II- IV clinical trials and monitoring studies from a scientific perspective.
• Previous authoring/co-authoring of clinical study protocols, ICFs, scientific study-related documents (e.g., study committee charters).
• Experience working in a cross-functional environment and able to coordinate cross-functional activities.
• 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.

Would you like to learn more about CTC and the opportunity outlined? Please, get in contact with us: you may either use the 'apply now' button, or write an email to us.