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 OfficeSenior
Nejo AI Summary
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
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 OfficeSenior
Nejo AI Summary
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
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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