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Director, CDPC Cluster Head Central Europe & MEA(m/w/x)
Strategic leadership for clinical studies in healthcare, life science, and electronics. 10+ years clinical research experience and 5+ years people management required. Oversight of operational aspects and investigator relationships.
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 in clinical research or equivalent
- Strategic thinking considering overall business objectives
- Outstanding leadership skills across teams and geographies
- Ability to work independently on complex tasks
- Excellent risk assessment, problem-solving, and decision-making abilities
- Superior organizational ability and time management
- Adaptability to change and ability to adjust work methods
- Strong interpersonal skills with high cultural awareness
- Self-motivated and proactive, willing to take responsibility
- 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
- Oversee operational aspects of clinical studies
- Build strong relationships with investigators and sites
- Engage with internal stakeholders
- Ensure studies meet timelines and budgets
- Maintain high quality standards in studies
- Serve as company liaison with 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 FSP team members indirectly
- Manage clinical study budgets
- Maintain site relationships and performance
- Supervise local and regional studies
- Oversee company-sponsored clinical studies
- Manage Investigator-Sponsored Studies
- Coordinate Collaborative Research studies
- Administer Early Access Programs
Work Experience
- 10 years
Education
- Bachelor's degree
Languages
- French – Fluent
- English – Fluent
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Director, CDPC Cluster Head Central Europe & MEA(m/w/x)
Strategic leadership for clinical studies in healthcare, life science, and electronics. 10+ years clinical research experience and 5+ years people management required. Oversight of operational aspects and investigator relationships.
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 in clinical research or equivalent
- Strategic thinking considering overall business objectives
- Outstanding leadership skills across teams and geographies
- Ability to work independently on complex tasks
- Excellent risk assessment, problem-solving, and decision-making abilities
- Superior organizational ability and time management
- Adaptability to change and ability to adjust work methods
- Strong interpersonal skills with high cultural awareness
- Self-motivated and proactive, willing to take responsibility
- 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
- Oversee operational aspects of clinical studies
- Build strong relationships with investigators and sites
- Engage with internal stakeholders
- Ensure studies meet timelines and budgets
- Maintain high quality standards in studies
- Serve as company liaison with 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 FSP team members indirectly
- Manage clinical study budgets
- Maintain site relationships and performance
- Supervise local and regional studies
- Oversee company-sponsored clinical studies
- Manage Investigator-Sponsored Studies
- Coordinate Collaborative Research studies
- Administer Early Access Programs
Work Experience
- 10 years
Education
- Bachelor's degree
Languages
- French – Fluent
- English – Fluent
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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