Global Study Manager — Lead Clinical Trial Programs

KCR Placement

Madrid

Vor Ort

EUR 70.000 - 110.000

Vollzeit

14 Tage+

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

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Zusammenfassung

ICON Strategic Solutions is seeking a Global Study Manager to lead trial operations from sponsor projects. You will manage day-to-day clinical trial activities and support teams to deliver high-quality outcomes across our programmes.

The role requires driving clinical deliverables, strong collaboration with cross-functional teams, and building relationships with investigators. Willingness to travel ~25% is expected.

Qualifikationen

  • University degree in medicine, science, or equivalent combination of education & experience.
  • Demonstrated ability to drive the clinical deliverables of a study.
  • Subject matter expertise in the designated therapeutic area.
  • Prior monitoring experience is preferred.
  • Willingness to travel as required (approximately 25%)

Aufgaben

  • Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards.
  • Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.
  • Build and manage strong relationships with trial investigators and stakeholders.
  • Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines.
  • Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.

Kenntnisse

Clinical trial management
Team leadership
Budget management
Regulatory compliance
Vendor management
Stakeholder management
Monitoring experience

Ausbildung

University degree in medicine, science, or equivalent combination of education & experience

Jobbeschreibung

ICON Strategic Solutions is seeking a Global Study Manager to lead trial operations from sponsor projects. You will manage day-to-day clinical trial activities and support teams to deliver high-quality outcomes across our programmes.

The role requires driving clinical deliverables, strong collaboration with cross-functional teams, and building relationships with investigators. Willingness to travel ~25% is expected.

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