Dein persönlicher KI-Karriere-Agent
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.
Anforderungen
- 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%
Aufgaben
- 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
Berufserfahrung
- 10 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Französisch – fließend
- Englisch – fließend
Noch nicht perfekt?
- EMD SeronoVollzeitmit HomeofficeSeniorEysins
- 8933 DuPont Specialty Products Operations Sarl
EH&S Leader(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenMeyrin - 8933 DuPont Specialty Products Operations Sarl
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Vollzeitmit HomeofficeBerufserfahrenMeyrin - Philips
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Vollzeitmit HomeofficeSeniorGland
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.
Anforderungen
- 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%
Aufgaben
- 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
Berufserfahrung
- 10 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Französisch – fließend
- Englisch – fließend
Über das Unternehmen
SUSONITY
Branche
Healthcare
Beschreibung
Das Unternehmen entwickelt Medikamente, intelligente Geräte und innovative Technologien in Therapiegebieten wie der Onkologie, Neurologie und Fruchtbarkeit.
Noch nicht perfekt?
- EMD Serono
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Vollzeitmit HomeofficeBerufserfahrenMeyrin - 8933 DuPont Specialty Products Operations Sarl
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Vollzeitmit HomeofficeBerufserfahrenMeyrin - Philips
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