Job Title: Senior Clinical Operations Manager
Work Location: Allschwil
Country: Switzerland
Schedule: Full-time (100%)
Duration: 12 months Contractor
Rate: CHF 94.91
The Senior Clinical Operations Manager supervises all operational trial-related activities and the operations team assigned to the trial. The Senior Clinical Operations Manager is accountable for ensuring the delivery of global operational outputs in accordance with the trial timelines and quality standards.
Job Responsibilities
Provide operational input to the project planning, trial plans, and any activity affecting the operational performance and quality of the trial.
Report all operational aspects of the trial to the Clinical Trial Team (CTT) leader.
Lead the operational planning and trial-related activities in close collaboration with other functions. Supervise the external operations team assigned to the trial, provide clear instructions, and set priorities.
Supervise resolution of operational issues proactively and timely.
Supervise the selection and management of External Service Providers (ESPs) and Clinical Research Organizations (CROs), and develop trial-related operational documents.
Manage clinical trial supplies in collaboration with Technical Operations: forecasting, ordering, distribution, import/export licenses.
Oversee information on operational clinical trial activities for reporting to the CTT, including critical issues and key performance indicators.
Ensure adequate trial-specific training is provided to the assigned operations team and CRO/ESPs. Supervise the Study Master File (SMF) to ensure completeness and readiness for audit/inspection. Contribute by performing ongoing quality checks/reviews.
Participate actively in Investigator meeting preparations and presentations, and in Site Selection Visits (SSVs) and Site Initiation Visits (SIVs), as necessary.
Support business units/departments in internal audit preparations and during audits, and ensure follow-up and resolution of audit findings related to operational activities.
Candidate Requirements
Bachelor of Science degree or equivalent University degree in life sciences or healthcare.
7 years of experience managing operational aspects of complex Phase II and Phase III clinical trials and global teams.
Experience leading global cross-functional (matrix) and multicultural teams.
Ability to represent Clinical Operations in high-level Clinical Development meetings.
Extensive experience in selecting and managing External Service Providers (ESPs), including performance assessments and financial management.
Previous experience working with electronic data capture, electronic Trial Master File (eTMF), and Clinical Trial Management Systems (CTMS).
Excellent knowledge of ICH-GCP.
Advanced computer skills (e.g., Microsoft Office, Word, Excel, PowerPoint).
Excellent verbal and written communication skills in English; strong cultural knowledge of national diversities.
Position may require international travel.
Strong project management expertise (including risk management and contingency planning).
Self-motivated and able to work independently and effectively in a matrix/team environment.
Goal-oriented, able to prioritize and execute tasks effectively in a high-pressure environment.
Strong problem-solving skills.
Please apply here and Harry Henson will be in touch with further details!
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