Contract Clinical Operations Manager - Global Healthcare - Switzerland

RBW Consulting are proud to be working with a leading global healthcare organisation who are uniquely positioned to bridge the traditional divide between generics and brands, combining the best of both, to more holistically address healthcare needs globally.

We are seeking an experienced Clinical Operations Manager on a 12 months, 1 FTE contract to join this industry leader and work on their hybrid model of 3 days per week office based in Allschwil and 2 days per week at home based.

The hourly rate for this role is CHF 69.49.

The Clinical Operations Manager is driving the development of the operational trial related documents and procedures, as well as setting-up the ESPs and supervising the deliverables of all ESP related activities, from specifications to close-out.

For large Phase III or complicated trials, several Clinical Operations Managers might be assigned to a trial for the management of ESPs.

Manage the operational trial related activities in close collaboration with other functions, such as : site initiations, site closures, import / export licenses for materials and IMP, eTMF set-up and maintenance, contracts execution and invoices, submissions to Health Authorities, submissions to Ethics Committees / Institutional Review Boards (ECs / IRBs), timely completion of electronic Case Report Forms (eCRFs), Source Data verification (SDV) progress and query responses timelines

Manage the selection of ESPs in collaboration with other functions

Lead the development of ESP specifications, testing and implementation in collaboration with other functions, and ensure appropriate quality control of deliverables

Supervise the deliverables towards the Contract Research Organization (CRO) and ESPs selected for the trial, to ensure compliance with study protocol and in accordance with scope of work;

identify areas of concern and escalate to the Clinical Trial team (CTT)

Lead the development of trial-related operational documents

Consolidate information on operational clinical trial level activities for reporting to the CTT by the Senior Clinical Operations Manager (including critical issues and key performance indicators)

Resolve operational issues in a proactive and timely fashion

Act as the communication channel for the Clinical Research Associates (CRAs) to ensure data quality is maintained, in close collaboration with other CTT functions

Approve invoices (e.g. site payments) and ensure related payments in a timely manner

Contribute to the Study Master File (StMF) completeness and readiness for audit / inspection and by performing ongoing quality checks / review

Actively participate to Investigators meeting preparation and presentations and in Site Selection Visits and Site Initiation Visits, as necessary

Mentor team members as needed

Assume responsibility for other project or trial-related duties as assigned

Requirements

Bachelor of Science degree or equivalent University degree in life sciences or healthcare

4 years of experience in managing operational aspects of Phase II and Phase III trials and executing a wide range of clinical trial activities from study start up to clinical study report

Experience in working in global cross-functional (matrix) and multicultural teams

Experience in selecting and managing External Service Providers (ESP), including performance assessments and finance management

Previous experience working with electronic data capture, electronic Trial Master File (eTMF), and Clinical Trial Management Systems (CTMS)

Excellent knowledge of International Conference on Harmonization-Good Clinical Practice (ICH-GCP) guidelines Strong computer skills including proficiency in Microsoft (MS)-based applications (e.

g., Word, Excel, and PowerPoint)

Excellent verbal and written communication skills in English; strong cultural knowledge of national diversities

Position may require international travel

Please apply here and Harry Henson will be in touch to discuss your application further.