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Executive Director, Clinical Operations, Europe(m/w/x)
Description
In this role, you will lead the Clinical Operations team to design and execute clinical trials, ensuring efficient processes and compliance. Your day-to-day responsibilities will involve collaborating with various departments, managing resources, and driving patient recruitment to support the growing pipeline.
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Requirements
- •Thorough knowledge of biopharmaceutical drug development
- •Excellent understanding of pharmaceutical business operations
- •Deep understanding of CRO processes
- •Big-picture executive mindset
- •Well-rounded personality with strong executive presence
- •Strategic networking skills
- •MSc/PhD or MD with significant experience in Clinical Operations
- •Strong leadership skills in biopharmaceutical industry
- •Therapeutic area knowledge in oncology clinical development
- •Track record of managing clinical operations
- •Solid track record with CROs
- •Deep understanding of clinical development
- •Experience defining and executing global R&D strategies
- •Demonstrated leadership in clinical operations
- •Experience leading clinical trials and managing vendors
- •Excellent knowledge of FDA, EMA & ICH/GCP regulations
- •Ability to work in a team environment
- •Entrepreneurial experience with drive and bias for action
- •Comfortable leading through others
- •Experience in a collaborative, matrix-based organisation
- •Ability to influence externally
- •Ability to operate with high independence
- •Excellent networking and leadership skills
- •Passionate, curious, entrepreneurial self-starter
- •Strategic and analytical mindset
- •Unquestionable integrity and high ethical standards
Education
Work Experience
15 years
Tasks
- •Build a Clinical Operations organization for clinical trials
- •Contribute to clinical trial strategy and management
- •Manage operational and logistical tasks for clinical development
- •Coordinate internal and external resources for patient recruitment
- •Communicate with countries, CROs, and vendors about trial updates
- •Create and implement SOPs for clinical trials
- •Implement process improvements based on trial needs and feedback
- •Work with trial sites to expedite patient recruitment
- •Provide leadership and mentorship to the clinical operations team
- •Support team members in prioritizing work and solving trial issues
- •Provide regular updates and status reports to senior management
- •Monitor CRO performance according to functional metrics
- •Maintain a positive, results-oriented work environment
- •Ensure compliance with applicable regulations
- •Oversee regulatory processes and quality assurance for studies
Languages
English – Business Fluent
- Revolution MedicinesFull-timeOn-siteSeniorBasel
- BeOne Medicines I GmbH
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Executive Director, Clinical Operations, Europe(m/w/x)
The AI Job Search Engine
Description
In this role, you will lead the Clinical Operations team to design and execute clinical trials, ensuring efficient processes and compliance. Your day-to-day responsibilities will involve collaborating with various departments, managing resources, and driving patient recruitment to support the growing pipeline.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Thorough knowledge of biopharmaceutical drug development
- •Excellent understanding of pharmaceutical business operations
- •Deep understanding of CRO processes
- •Big-picture executive mindset
- •Well-rounded personality with strong executive presence
- •Strategic networking skills
- •MSc/PhD or MD with significant experience in Clinical Operations
- •Strong leadership skills in biopharmaceutical industry
- •Therapeutic area knowledge in oncology clinical development
- •Track record of managing clinical operations
- •Solid track record with CROs
- •Deep understanding of clinical development
- •Experience defining and executing global R&D strategies
- •Demonstrated leadership in clinical operations
- •Experience leading clinical trials and managing vendors
- •Excellent knowledge of FDA, EMA & ICH/GCP regulations
- •Ability to work in a team environment
- •Entrepreneurial experience with drive and bias for action
- •Comfortable leading through others
- •Experience in a collaborative, matrix-based organisation
- •Ability to influence externally
- •Ability to operate with high independence
- •Excellent networking and leadership skills
- •Passionate, curious, entrepreneurial self-starter
- •Strategic and analytical mindset
- •Unquestionable integrity and high ethical standards
Education
Work Experience
15 years
Tasks
- •Build a Clinical Operations organization for clinical trials
- •Contribute to clinical trial strategy and management
- •Manage operational and logistical tasks for clinical development
- •Coordinate internal and external resources for patient recruitment
- •Communicate with countries, CROs, and vendors about trial updates
- •Create and implement SOPs for clinical trials
- •Implement process improvements based on trial needs and feedback
- •Work with trial sites to expedite patient recruitment
- •Provide leadership and mentorship to the clinical operations team
- •Support team members in prioritizing work and solving trial issues
- •Provide regular updates and status reports to senior management
- •Monitor CRO performance according to functional metrics
- •Maintain a positive, results-oriented work environment
- •Ensure compliance with applicable regulations
- •Oversee regulatory processes and quality assurance for studies
Languages
English – Business Fluent
About the Company
Revolution Medicines
Industry
Pharmaceuticals
Description
The company is a clinical-stage precision oncology company focused on developing novel targeted therapies for RAS-addicted cancers.
- Revolution Medicines
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