Global Study Lead, Clinical Trials & Strategy

Roche Holding AG; Tucson (AZ); On-site; USD 90,000 - 186,000; Full time

Job summary

Roche Holding AG in Tucson, AZ, seeks a Global Study Lead to design, execute, monitor and close studies within time and budget, coordinating with internal teams and external CROs to ensure compliance and quality.

You will lead the study team, develop evidence generation scenarios with cross-functional partners, and oversee study documents and budgets. The role requires extensive clinical operations expertise and a track record in sponsored studies and publications.

Qualifications

• Bachelor's degree in Life Sciences or related field.
• 5+ years of experience managing the full lifecycle of sponsored studies.
• Experience publishing study results with the Publication Team.
• Knowledge of Clinical Operations in product development and Roche's market position.
• PHCS/Companion Diagnostic studies experience with Pharma partners or CROs.
• Analytical thinking and ability to assess risks and solve problems.

Responsibilities

• Lead global study team with accountability for quality, budget and timelines.
• Collaborate with Regulatory Affairs, R&D and cross-functional teams to plan evidence generation scenarios.
• Develop key study documents (Design Validation Plan, protocol, study forms).
• Oversee planning of companion diagnostics studies sponsored by Pharma partners.
• Accountable for study-level budgets and adherence to regulations and audits.
• Publish study results in collaboration with the Publication Team.

Skills

Project management

Cross-functional collaboration

Clinical operations

Budget planning

Regulatory compliance

Education

Bachelor's degree in Life Sciences or related field

Advanced degree in Life Sciences or related field

Job description

Roche Holding AG in Tucson, AZ, seeks a Global Study Lead to design, execute, monitor and close studies within time and budget, coordinating with internal teams and external CROs to ensure compliance and quality.

You will lead the study team, develop evidence generation scenarios with cross-functional partners, and oversee study documents and budgets. The role requires extensive clinical operations expertise and a track record in sponsored studies and publications.