Senior Clinical Trial Scientist — Protocols & Monitoring

CTC Resourcing Solutions AG; Basel; Vor Ort; CHF 120.000 - 180.000; Vollzeit

Zusammenfassung

CTC Resourcing Solutions AG is recruiting a Senior Clinical Trial Scientist for a 12-month contract based in the Basel area. You will develop expertise in the science behind the indication and lead delivery of trial protocols and related documents.

You will provide input to cross-functional trial documents, monitor data during the study, and manage study committees while collaborating with external experts as needed.

Qualifikationen

• Relevant Swiss work permit/residency required.
• PhD, PharmD, MSc or equivalent in life/health sciences.
• 5+ years in clinical development within CRO or pharma.
• Experience planning/setting up/monitoring phase II–IV trials.
• Authoring of study protocols, ICFs, or related documents.

Aufgaben

• Develop deep understanding of the science behind the indication and trial.
• Deliverables include the clinical trial protocol and related documents.
• Review cross-functional trial documents (SAP, ESP specs, monitoring guidelines).
• Perform data review and medical monitoring during trial conduct.
• Manage study committees and oversight structures.

Kenntnisse

Cross-functional collaboration

Scientific writing

Regulatory knowledge

English communication

Clinical trial monitoring

Ausbildung

PhD/PharmD/MSc in life or health sciences

Jobbeschreibung

CTC Resourcing Solutions AG is recruiting a Senior Clinical Trial Scientist for a 12-month contract based in the Basel area. You will develop expertise in the science behind the indication and lead delivery of trial protocols and related documents.

You will provide input to cross-functional trial documents, monitor data during the study, and manage study committees while collaborating with external experts as needed.