EMD Serono
Sr. Director, Compound Operational Lead(m/w/x)
Full-timeWith HomeofficeSenior
Eysins
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SUSUSONITY
Director, CDPC Cluster Head Central Europe & MEA(m/w/x)
Eysins
Full-timeWith Home OfficeManagement
Nejo AI Summary
Strategic leadership for clinical studies in Healthcare, Life Science, and Electronics. 10+ years clinical research experience required. Oversight of 260+ care facilities, 4-day work week.
Requirements
- 10+ years professional experience in Clinical Research
- At least 5 years people and resource management
- Experience in Clinical Trial Management and managing Clinical Monitoring/Site Management
- Medical or Life Sciences degree or equivalent
- Strategic thinking beyond own function
- Outstanding leadership skills
- Ability to work independently on complex tasks
- Excellent risk assessment, problem-solving, decision-making abilities
- Superior organizational ability
- Adaptability to change
- Strong interpersonal skills with high cultural awareness
- Self-motivated and proactive
- Ability to work effectively in a matrix organization
- Willingness to travel domestically and internationally/regionally up to 30%
Tasks
- Provide strategic leadership for clinical studies
- Ensure operational oversight in assigned region
- Build strong relationships with investigators and sites
- Engage with internal stakeholders
- Deliver studies on time and within budget
- Maintain highest quality standards
- Serve as interface between company and external partners
- Align global and local priorities
- Enhance CDPC performance through strategic recommendations
- Manage direct reports including CSLs, CRMs, CRAs, and SSUM
- Provide strategic direction to site-facing teams
- Support site-level activities
- Resolve operational challenges
- Oversee Full Service Provider team members
- Manage budget for clinical studies
- Maintain site relationships and performance
- Oversee local and regional studies
- Manage company-sponsored clinical studies
- Supervise Investigator-Sponsored Studies
- Coordinate Collaborative Research studies
- Administer Early Access Programs
Work Experience
- 10 years
Education
- Bachelor's degree
Languages
- French – Business Fluent
- English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of SUSONITY 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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SUSUSONITY
Director, CDPC Cluster Head Central Europe & MEA(m/w/x)
Eysins
Full-timeWith Home OfficeManagement
Nejo AI Summary
Strategic leadership for clinical studies in Healthcare, Life Science, and Electronics. 10+ years clinical research experience required. Oversight of 260+ care facilities, 4-day work week.
Requirements
- 10+ years professional experience in Clinical Research
- At least 5 years people and resource management
- Experience in Clinical Trial Management and managing Clinical Monitoring/Site Management
- Medical or Life Sciences degree or equivalent
- Strategic thinking beyond own function
- Outstanding leadership skills
- Ability to work independently on complex tasks
- Excellent risk assessment, problem-solving, decision-making abilities
- Superior organizational ability
- Adaptability to change
- Strong interpersonal skills with high cultural awareness
- Self-motivated and proactive
- Ability to work effectively in a matrix organization
- Willingness to travel domestically and internationally/regionally up to 30%
Tasks
- Provide strategic leadership for clinical studies
- Ensure operational oversight in assigned region
- Build strong relationships with investigators and sites
- Engage with internal stakeholders
- Deliver studies on time and within budget
- Maintain highest quality standards
- Serve as interface between company and external partners
- Align global and local priorities
- Enhance CDPC performance through strategic recommendations
- Manage direct reports including CSLs, CRMs, CRAs, and SSUM
- Provide strategic direction to site-facing teams
- Support site-level activities
- Resolve operational challenges
- Oversee Full Service Provider team members
- Manage budget for clinical studies
- Maintain site relationships and performance
- Oversee local and regional studies
- Manage company-sponsored clinical studies
- Supervise Investigator-Sponsored Studies
- Coordinate Collaborative Research studies
- Administer Early Access Programs
Work Experience
- 10 years
Education
- Bachelor's degree
Languages
- French – Business Fluent
- English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of SUSONITY 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
SUSONITY
Industry
Healthcare
Description
Das Unternehmen entwickelt Medikamente, intelligente Geräte und innovative Technologien in Therapiegebieten wie der Onkologie, Neurologie und Fruchtbarkeit.
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