Contract Clinical Operations Coordinator - Switzerland - 1 FTE

RBW Consulting are partnering with a leading Biopharmaceutical organisation in their search for a Contract Clinical Operations Coordinator in Switzerland.

This company discovers, develops, and commercializes medicines across a wide variety of therapeutic areas.

This role will be a 12 month, 1 FTE contract and you will be required in the office in Allschwil, Switzerland.

Job Responsibilities

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 (e.g., forms, guidelines)

Coordinate the preparations and / or review of site related documents (e.g., Investigator Site Files (ISF)

Coordinate the preparation and distribution of the clinical study documentation (e.g., site communication, newsletters, pocket brochures, appendix 16 for the Clinical Study Report (CSR)

Coordinate the delivery and inventory of study related non-clinical supplies (ordering, distribution, tracking, expiry dates management, resupplies

Coordinate site contracts finalization and execution

Coordinate Insurance certificates for the trial in collaboration with legal department

Ensure completeness and maintenance of key trial information in the Clinical Trial Management System (CTMS

File and upload documents in the different systems as needed

Ensure accurate maintenance and archiving of the electronic Master File (eTMF) within the required timelines and contribute by performing ongoing quality checks / review

Function as a Study Owner in the eTMF when require

Assist in reviewing and providing feedback of Standard Operations Procedures (SOPs), Working Instructions (WISs) and processes

Schedule and organize functional group meetings and / or events as needed

Support the Clinical Trial Teams, including the Global Strategic Sourcing Group as needed (e.g. 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

Candidates Requirements

Minimum 2 years of clinical research experience is preferred

Strong English written and verbal skills

Ability to work independently

Ability to effectively handle multiple priorities in a fast-paced environment

Ability to find effective solutions when faced with difficult situations and to implement team decisions

Strong computer skills, including proficiency in Microsoft (MS)-based applications (e.g., Word, Excel, and PowerPoint)

Apply here to find out more!