Global Studies Leader (GSL)
Roche is seeking a Global Studies Leader (GSL) to join the Product Development Global Clinical Operations (PDG) team in Welwyn, UK. As a GSL, you’ll play a pivotal role in delivering one or more clinical studies (Phases Ib-IV), helping bring transformative medicines to patients worldwide. This high-impact leadership role involves directing cross-functional study teams, ensuring timelines, budgets, and quality standards are met. You'll be responsible for study planning, risk management, vendor oversight, and inspection readiness while fostering a high-performing, collaborative team culture. You’ll work closely with internal stakeholders and CRO partners to align clinical trials with Roche’s ambitious Pharma 2030 goals. If you’re a strategic thinker with deep clinical research expertise and a passion for improving patient outcomes, this is your opportunity to shape the future of global healthcare through operational excellence and innovation in clinical development.
International/domestic travel may be required)
Requirements
1. University degree in medical, biological sciences, or related clinical research field
2. Significant clinical R&D experience within the pharmaceutical industry
3. Proven track record in leading global clinical trials
4. In-depth knowledge of regulatory and clinical study management processes
5. Strong leadership, interpersonal, and communication skills
6. Strategic mindset with excellent critical thinking and problem-solving abilities
7. Experience with budget oversight and vendor management
8. People leadership experience is preferred
9. Willingness to travel domestically and internationally as needed
Benefits
1. Opportunity to lead impactful global studies in a mission-driven organization
2. Collaborate with top scientific and clinical experts worldwide
3. Inclusive and respectful culture that embraces diversity
4. Career development and learning opportunities
5. Competitive compensation and benefits package
6. Flexible working arrangements reviewed case-by-case
7. Join a team contributing to the advancement of transformative medicines
Responsibilities
1. Lead and manage global cross-functional clinical study teams
2. Oversee clinical trial delivery from planning through closeout
3. Ensure compliance with timelines, budget, and quality standards
4. Collaborate with CROs to implement quality risk strategies and study plans
5. Maintain inspection-readiness and act as primary contact for audits
6. Manage and monitor external service provider performance and contracts
7. Drive process improvement and contribute to clinical operations innovation
8. Foster a culture of feedback, growth, and high performance among team members
9. Influence and collaborate across internal and external stakeholders globally
The application process will continue on the employer's website.
Location
Welwyn, Hertfordshire, United Kingdom
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