Debiopharm
Clinical Operational Manager (COM)(m/w/x)
Full-timeOn-siteSenior
Lausanne
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DEDebiopharm
Clinical Operational Specialist (COS)(m/w/x)
Lausanne
Full-timeFreelanceOn-siteExperienced
Nejo AI Summary
Managing clinical trial operations and deliverables for cancer and infectious disease therapies. 3 years of clinical research experience in pharma required. Equal-pay certified workplace, inclusive culture.
Requirements
- Bachelor's or Master's Degree in Science or Healthcare
- 3 years in pharmaceutical industry, preferably clinical research
- High organization and task prioritization
- Collaborative, flexible, proactive attitude
- Very good communication skills
- Fluent English
- French or other European languages are a plus
Tasks
- Manage Clinical Trial Team meetings
- Prepare meeting minutes
- Follow up on outstanding actions
- Ensure operational trial deliverables meet timelines, budget, and quality standards
- Collect and track trial status
- Monitor trial progress
- Update internal and external boards
- Collaborate with TMF Specialists
- Set up and maintain Trial Master File
- Ensure audit readiness
- Manage IRB/IEC submission plans
- Set up clinical trial insurance
- Oversee vendor systems setup and management
- Assist with CRO/vendor oversight
- Track CRO/vendor performance
- Reconcile invoices
- Generate purchasing orders
- Prepare materials for investigator meetings
- Prepare materials for advisory boards
- Prepare internal newsletters
Work Experience
- 3 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Fluent
- French – 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
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Debiopharm and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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DEDebiopharm
Clinical Operational Specialist (COS)(m/w/x)
Lausanne
Full-timeFreelanceOn-siteExperienced
Nejo AI Summary
Managing clinical trial operations and deliverables for cancer and infectious disease therapies. 3 years of clinical research experience in pharma required. Equal-pay certified workplace, inclusive culture.
Requirements
- Bachelor's or Master's Degree in Science or Healthcare
- 3 years in pharmaceutical industry, preferably clinical research
- High organization and task prioritization
- Collaborative, flexible, proactive attitude
- Very good communication skills
- Fluent English
- French or other European languages are a plus
Tasks
- Manage Clinical Trial Team meetings
- Prepare meeting minutes
- Follow up on outstanding actions
- Ensure operational trial deliverables meet timelines, budget, and quality standards
- Collect and track trial status
- Monitor trial progress
- Update internal and external boards
- Collaborate with TMF Specialists
- Set up and maintain Trial Master File
- Ensure audit readiness
- Manage IRB/IEC submission plans
- Set up clinical trial insurance
- Oversee vendor systems setup and management
- Assist with CRO/vendor oversight
- Track CRO/vendor performance
- Reconcile invoices
- Generate purchasing orders
- Prepare materials for investigator meetings
- Prepare materials for advisory boards
- Prepare internal newsletters
Work Experience
- 3 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Fluent
- French – 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
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Debiopharm and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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.
Not a perfect match?
- Debiopharm
Clinical Operational Manager (COM)(m/w/x)
Full-timeOn-siteSeniorLausanne - Debiopharm
Senior Trial Master File (TMF) Specialist(m/w/x)
Full-timeOn-siteSeniorLausanne - Debiopharm
Pharmaceutical Quality (pQM) Specialist(m/w/x)
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Regulatory Affairs Specialist(m/w/x)
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Associate Safety Physician(m/w/x)
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