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SUSUSONITY

Director, CDPC Cluster Head Central Europe & MEA(m/w/x)

Eysins
Vollzeitmit HomeofficeSenior

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

  • Französischfließend
  • Englischfließend
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