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Clinical Operational Manager (COM)(m/w/x)
Managing clinical operations for cancer and infectious disease therapies, coordinating cross-functional teams and overseeing CRO/vendor performance. 5+ years in pharma matrix organizations, with 3+ years in clinical trials, required. Equal-pay certified workplace, inclusive culture.
Requirements
- Bachelor's or Master's Degree in Science or Healthcare
- Minimum 5 years in pharmaceutical industry in matrix organization(s)
- At least 3 years specifically in clinical trials
- Experience managing complex cross-border studies
- Experience dealing with external vendors is a serious asset
- Excellent communication skills
- Strong leadership skills
- Influencing skills
- Drive
- Proactivity
- Self-starter
- Flexibility
- Project management skills
- Analytical skills
- Fluent in English
- French or other European languages are a plus
Tasks
- Coordinate and lead cross-functional teams
- Organize and track critical actions
- Oversee CRO/vendor performance
- Manage delegated operational activities and plans
- Ensure trial deliverables meet timelines, budget, and quality standards
- Manage trial documentation in the TMF
- Collect and track trial status
- Monitor enrolment and timelines
- Update internal and external boards
- Coordinate with Clinical Trial Supply Managers
- Ensure IMP reaches regions and countries effectively
- Contribute to risk and issue identification
- Develop mitigation and corrective plans
- Ensure compliance with GCP
- Maintain inspection readiness
Work Experience
- 5 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Fluent
- French – Basic
- Basque – Basic
Benefits
Other Benefits
- Equal-Pay certified workplace
Informal Culture
- Inclusive and respectful workplace
Purpose-Driven Work
- Culture that values people, purpose, and performance
Startup Environment
- Opportunity to grow, share, and shape the future of healthcare
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Clinical Operational Manager (COM)(m/w/x)
Managing clinical operations for cancer and infectious disease therapies, coordinating cross-functional teams and overseeing CRO/vendor performance. 5+ years in pharma matrix organizations, with 3+ years in clinical trials, required. Equal-pay certified workplace, inclusive culture.
Requirements
- Bachelor's or Master's Degree in Science or Healthcare
- Minimum 5 years in pharmaceutical industry in matrix organization(s)
- At least 3 years specifically in clinical trials
- Experience managing complex cross-border studies
- Experience dealing with external vendors is a serious asset
- Excellent communication skills
- Strong leadership skills
- Influencing skills
- Drive
- Proactivity
- Self-starter
- Flexibility
- Project management skills
- Analytical skills
- Fluent in English
- French or other European languages are a plus
Tasks
- Coordinate and lead cross-functional teams
- Organize and track critical actions
- Oversee CRO/vendor performance
- Manage delegated operational activities and plans
- Ensure trial deliverables meet timelines, budget, and quality standards
- Manage trial documentation in the TMF
- Collect and track trial status
- Monitor enrolment and timelines
- Update internal and external boards
- Coordinate with Clinical Trial Supply Managers
- Ensure IMP reaches regions and countries effectively
- Contribute to risk and issue identification
- Develop mitigation and corrective plans
- Ensure compliance with GCP
- Maintain inspection readiness
Work Experience
- 5 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Fluent
- French – Basic
- Basque – Basic
Benefits
Other Benefits
- Equal-Pay certified workplace
Informal Culture
- Inclusive and respectful workplace
Purpose-Driven Work
- Culture that values people, purpose, and performance
Startup Environment
- Opportunity to grow, share, and shape the future of healthcare
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Debiopharm
Industry
Pharmaceuticals
Description
Debiopharm is a privately-owned Swiss biopharmaceutical company committed to research in oncology and infectious diseases to improve patient outcomes and quality of life.
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