Not specified; details provided based on primary p...
Not specified (assumed to be hybrid based on current industry trends).
7 years clinical r&d experience
2 years project management experience
Ich-gcp compliance knowledge
Roche is seeking a Global Studies Leader to oversee the operational components of clinical studies from Phase Ib-IV, ensuring alignment with strategy, timelines, and budget. The ideal candidate should have extensive experience in clinical research, strong project management skills, and the ability to collaborate effectively with cross-functional teams and external partners
Job Summary
The Global Studies Leader is accountable for delivering operational components of clinical studies from Phase Ib-IV in line with strategy, timelines, and budget.
This role requires leading cross-functional Study Management Teams to oversee the delivery of a clinical protocol from synopsis through study close while ensuring ICH-GCP compliance.
Roche fosters a culture of personal expression and open dialogue where employees are valued and respected for their unique qualities.
Matching Summary
Match Score: 85
Roche is seeking a Global Studies Leader to oversee the operational components of clinical studies from Phase Ib-IV, ensuring alignment with strategy, timelines, and budget. The ideal candidate should have extensive experience in clinical research, strong project management skills, and the ability to collaborate effectively with cross-functional teams and external partners.
Salary
Not specified; details provided based on primary posting location later in hiring process
Skills & Requirements
Must-have
7 years clinical R&D experience
2 years project management experience
ICH-GCP compliance knowledge
Cross-functional team leadership
CRO partnership management
Study budget oversight
Nice-to-have
Strategic critical thinking abilities
Innovation in clinical operations
Patient-centric approach mindset
Health equity research commitment
Strong conflict management skills
Key Requirements
University degree in medical or biological sciences
Minimum 7 years relevant clinical experience in pharmaceutical industry
Minimum 2 years project management experience
Extensive knowledge of clinical research regulatory requirements