Clinical Operations Coordinator

CK Group; Basel; Vor Ort; Vollzeit

Zusammenfassung

A leading global pharmaceutical company is seeking a Clinical Operations Coordinator for a 12-month contract in Switzerland. The role involves overseeing clinical trials, preparing essential documents, and supporting trial procedures. Ideal candidates should have at least 2 years of clinical research experience and be able to manage multiple priorities efficiently.

Qualifikationen

• Minimum 2 years of clinical research experience is preferred.
• Ability to effectively handle multiple priorities in a fast-paced environment.

Aufgaben

• Assist the clinical operations team in managing clinical trials.
• Coordinate the preparation and review of trial-related documents.
• Ensure maintenance of key trial information in the Clinical Trial Management System (CTMS).

Kenntnisse

Clinical research

Project management

Quality assurance

Jobbeschreibung

Job Title : Clinical Operations Coordinator

Duration : 12 months initial contract

Salary : CHF61 phr

CK QLS are recruiting for Clinical Operations Coordinator, to join a growing global pharmaceutical company, on a permanent role in Switzerland.

Clinical Operations Coordinator Role :

• Assists the clinical operations team in the operational management and oversight of clinical trials, during set-up, conduct and until archiving, for an assigned trial.
• Coordinate the preparation and / or review of all operational trial-related documents (forms, guidelines).
• Coordinate the preparations and / or review of site related documents (Investigator Site Files- ISF).
• Coordinate the preparation and distribution of the clinical study documentation (site communication, newsletters, pocket brochures, appendix 16 for the Clinical Study Report -CSR).

Further Responsibilities will Include :

• Ensure completeness and maintenance of key trial information in the Clinical Trial Management System (CTMS).
• Ensure accurate maintenance and archiving of the electronic Master File (eTMF) within the required timelines and contribute by performing ongoing quality checks / review.
• Support the Clinical Trial Teams, including the Global Strategic Sourcing Group (Issuing of confidentiality agreements (CDAs), contracts execution and shipment, issuing of change orders, Resource Request management, coordination of the providers contracts, processing of invoices in the system).
• Minimum 2 years of clinical research experience is preferred.
• Ability to effectively handle multiple priorities in a fast-paced environment.

Apply :

Please could you send any correspondence in English. Please quote job reference in all correspondence. It is essential that applicants hold entitlement to work in Switzerland.