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Senior Clinical Data Manager(m/w/x)
Designing eCRFs and setting up EDC systems for oncology and infectious disease drug development. 10+ years in clinical data management required. Equal-Pay certified workplace, inclusive culture.
Requirements
- Scientific or technical university-level background
- Project Management certification is a plus
- At least 10 years in clinical data management
- Experience in matrix organization
- Solid experience in pharmaceutical industry
- Support for Phase 1 to 3 studies
- Project Management experience is an asset
- Strong experience with various EDC systems
- First experience or proficiency automating activities with AI
- Proven track record leading data management studies
- Proven track record leading data management teams
- Delivery of high-quality, regulatory-compliant databases
- Excellent organizational skills
- Excellent planning/coordination skills
- Proactivity
- Communication skills
- Tech savvy
- Savvy with Digital tools and AI
- Fluent in English
- Knowledge of French is a distinct asset
Tasks
- Lead and coordinate CDM activities
- Design eCRFs
- Set up EDC systems
- Conduct User Acceptance Testing (UAT)
- Release databases
- Review and generate data queries
- Ensure timely data capture
- Define and manage study timelines
- Prepare Data Management Plans (DMP)
- Review validation plans
- Ensure GCP, SOP, and regulatory compliance
- Oversee database lock, transfer, and archiving
- Collaborate with Clinical Trial Managers
- Work with other stakeholders in a matrix environment
Work Experience
- 10 years
Education
- Compulsory education
Languages
- English – Fluent
- French – Basic
Tools & Technologies
- EDC systems
- AI
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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Senior Clinical Data Manager(m/w/x)
Designing eCRFs and setting up EDC systems for oncology and infectious disease drug development. 10+ years in clinical data management required. Equal-Pay certified workplace, inclusive culture.
Requirements
- Scientific or technical university-level background
- Project Management certification is a plus
- At least 10 years in clinical data management
- Experience in matrix organization
- Solid experience in pharmaceutical industry
- Support for Phase 1 to 3 studies
- Project Management experience is an asset
- Strong experience with various EDC systems
- First experience or proficiency automating activities with AI
- Proven track record leading data management studies
- Proven track record leading data management teams
- Delivery of high-quality, regulatory-compliant databases
- Excellent organizational skills
- Excellent planning/coordination skills
- Proactivity
- Communication skills
- Tech savvy
- Savvy with Digital tools and AI
- Fluent in English
- Knowledge of French is a distinct asset
Tasks
- Lead and coordinate CDM activities
- Design eCRFs
- Set up EDC systems
- Conduct User Acceptance Testing (UAT)
- Release databases
- Review and generate data queries
- Ensure timely data capture
- Define and manage study timelines
- Prepare Data Management Plans (DMP)
- Review validation plans
- Ensure GCP, SOP, and regulatory compliance
- Oversee database lock, transfer, and archiving
- Collaborate with Clinical Trial Managers
- Work with other stakeholders in a matrix environment
Work Experience
- 10 years
Education
- Compulsory education
Languages
- English – Fluent
- French – Basic
Tools & Technologies
- EDC systems
- AI
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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