Senior Clinical Trial Ops Lead — Basel (Contract)

CTC Resourcing Solutions; Basel; Vor Ort; CHF 90.000 - 120.000; Vollzeit

Zusammenfassung

CTC Resourcing Solutions is recruiting a Senior Clinical Trial Assistant for a 24-month contract based in Basel, Switzerland. The role leads local medical activities, aligns with regional medical strategy, and collaborates with cross-functional teams to drive patient and business impact.

You will support Clinical Operations, manage consultancy agreements, oversee eTMF documentation, and coordinate meetings and vendor interactions while ensuring compliance with ICH-GCP and Swiss regulations.

Qualifikationen

• Swiss working/residency permit required.
• Bachelor’s degree required; Master’s preferred.
• 2 years of experience in clinical research or clinical operations.
• 2 years supporting global clinical trials within pharma/CRO.
• 1 year experience with eTMF, document filing and inspection readiness.
• ICH-GCP guidelines; fluent in English.

Aufgaben

• Provide senior operational and administrative support to Clinical Operations Managers and teams.
• Manage consultancy agreements, including POs and invoicing.
• Coordinate and maintain clinical trial insurance activities and renewals.
• Act as liaison between Clinical Operations, Finance, Legal, and external vendors.
• Plan and document international/regional study meetings and events (virtual and onsite).
• Support Value Transfer reconciliation and transparency reporting.
• Maintain eTMF documentation and conduct quality checks for inspection readiness.
• Perform other duties as assigned.

Kenntnisse

Fluent English

Cross-functional collaboration

Administrative support

Ausbildung

Bachelor's degree

Master's degree preferred

Tools

eTMF

Adobe Sign

PO management

Jobbeschreibung

CTC Resourcing Solutions is recruiting a Senior Clinical Trial Assistant for a 24-month contract based in Basel, Switzerland. The role leads local medical activities, aligns with regional medical strategy, and collaborates with cross-functional teams to drive patient and business impact.

You will support Clinical Operations, manage consultancy agreements, oversee eTMF documentation, and coordinate meetings and vendor interactions while ensuring compliance with ICH-GCP and Swiss regulations.