Global Studies Leader (GSL) at F. Hoffmann-La Roche Ltd - Poland

, England, United Kingdom -

Full Time

Start Date

Immediate

Expiry Date

29 Dec, 25

Salary

0.0

Posted On

30 Sep, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Leadership, Clinical Research, Project Management, Regulatory Requirements, Team Collaboration, Communication, Strategic Thinking, Problem Solving, Budget Management, Risk Management, Process Improvement, Interpersonal Skills, Influence, Decision Making, Quality Standards, Audit Readiness

Industry

Biotechnology Research

Description

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position At Roche/Genentech Pharma Product Development Global Clinical Operations (PDG), we are determined to transform drug development and realize our Pharma Ambition to deliver 20 transformative medicines addressing diseases with the highest societal burden by 2029. At Roche, we're dedicated to transforming drug development and delivering life-changing medicines to patients worldwide. The Product Development Global Clinical Operations team is at the heart of this mission, and we are looking for a Global Studies Leader to drive the operational execution of one or more clinical trials. This is a critical leadership position where you'll have a direct impact on our ability to bring transformative medicines to patients with high unmet medical needs. As a Global Studies Leader, you will lead and drive the delivery of clinical studies from Phase Ib-IV, ensuring they align with our strategic goals, timelines, budget, and quality standards. This role requires a strong leader who can effectively collaborate and influence across a wide network of internal and external partners. The Opportunity: Lead a cross-functional study management team, guiding decision-making and ensuring the study progresses according to timelines, budget, and quality standards. Develop and maintain in collaboration with CRO partners a quality risk strategy and other essential study plans to drive clinical study execution and oversight. Oversee the study budget throughout its lifecycle, including re-forecasting and identifying and mitigating any financial risks. Manage external service providers and their contractual obligations, ensuring they deliver within agreed-upon timelines and budgets. Ensure the study is always inspection-ready, acting as the primary point of contact during audits or inspections. Lead with a growth mindset, providing regular feedback to study team members to support their professional development and foster a high-performing organization. Contribute to process improvements and innovation in clinical operations to exceed industry best practices. Who you are: You are a strategic, collaborative, and influential leader with a passion for clinical research. You have a proven track record of successfully leading clinical studies and inspiring cross-functional teams. You hold a university degree, preferably in medical or biological sciences, or a discipline related to clinical research. You have a strong, relevant clinical experience in R&D within the pharmaceutical industry, including project management experience. You have extensive knowledge of clinical research regulatory requirements and demonstrated abilities in clinical study management processes. You have strong team leadership skills and the ability to build and maintain effective working relationships with internal and external stakeholders. You possess excellent communication and interpersonal skills, along with strong strategic, critical thinking, and problem-solving abilities. Experience in a people leadership role is preferred, as this role may include people management responsibilities. Some international and/or domestic travel may be required. This role is based onsite at our Welwyn, United Kingdom office. We have multiple headcounts available for this role. We look forward to your application. #ClinOps Who we are A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. The statements herein are intended to describe the general nature and level of work being performed by employees, and are not to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of Roche Products Ltd. At Roche Products we believe diversity drives innovation and we are committed to building a diverse and flexible working environment. All qualified applicants will receive consideration for employment without regard to race, religion or belief, sex, gender reassignment, sexual orientation, marriage and civil partnership, pregnancy and maternity, disability or age. We recognise the importance of flexible working and will review all applicants’ requests with care. At Roche difference is valued and we are proud to be an equal opportunity employer where you are encouraged to bring your whole self to work.

Responsibilities

Lead and drive the delivery of clinical studies from Phase Ib-IV, ensuring alignment with strategic goals, timelines, budget, and quality standards. Oversee the study budget, manage external service providers, and ensure the study is inspection-ready.