Country Study Manager (Local Delivery Lead)

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Country Study Manager (Local Delivery Lead)

We are seeking a Local Delivery Lead (LDL) to provide leadership and manage the activities of operational planning and delivery of Phase I-IV clinical trials in a specific country or cluster of countries; across all therapy areas (Rx and Vx) to the required quality standards, GSK written standards, local regulations and ICH GCP.

Responsibilities

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

• Leadership & Team Management: Provides matrix leadership and comprehensive project management to the local study team. Coordinates cross-functional experts, vendor staff, and external clinical site personnel from study planning through execution. Responsible for fostering collaboration, evaluating team performance, and delivering feedback to line management when necessary.
• Operational Oversight & Communication: Acts as the primary operational link between central and local study teams, medical, and regulatory staff. Facilitates alignment on feasibility, site selection, and local requirements. Ensuring that study systems (e.g., TMF) are complete and accurate, and progress is effectively reported to stakeholders.
• Delivery & Quality Assurance: Oversees that critical study timelines, recruitment targets, patient recruitment cycle times, data integrity, and audit quality are forecasted, monitored, and achieved. Provides troubleshooting and problem resolution support, identifies risks, and escalates issues as needed to maintain productive, efficient study delivery.
• Compliance & Documentation: Ensures all regulatory requirements are met by preparing and coordinating submissions of Clinical Study Applications and local Informed Consent Forms to Regulatory Authorities (RA) and Ethics Committees (ECs). Maintains ongoing communication and assists with audits and inspections of local clinical operations and study sites.
• Budget, Contracts & Monitoring: Estimates, tracks, and delivers against local study budgets. Advises on contract development with sites, CROs, and vendors, participates in negotiations, reviews and approves monitoring visit reports, and verifies that monitoring activities are completed according to plan. Supports financial and contractual compliance throughout the study lifecycle.
• Continuous Learning: Acquires and maintains knowledge related to study compounds, protocols, disease area pathology, local treatment guidelines, and healthcare system requirements. Continuously develops skills in GCP, SOPs, monitoring, site and project management, and shares best practices.

Why you?

Basic Qualifications & Skills:

We are looking for professionals with these required skills to achieve our goals:

• Bachelor’s degree or equivalent in a science‑related field (e.g., life sciences, medicine, clinical research, pharmacy).
• Solid operational knowledge of clinical research with experience in all stages of study lifecycle (start-up, recruitment and close out) and understanding of R&D and drug/vaccine development process.
• Demonstrated strength in problem‑solving, negotiation, conflict resolution, and stakeholder management in a matrix environment.
• Excellent communication and leadership skills, with the ability to collaborate effectively.
• Excellent planning, organisational, and project‑management skills, with the ability to operate effectively in a dynamic, fast‑changing environment.
• Strong knowledge of GCP/ICH and country‑specific regulations.

Preferred Qualifications & Skills:

Please note the following skills are not necessary, just preferred, if you do not have them, please still apply:

• Experience in oncology and/or respiratory therapeutic areas.
• Ability to lead cross-functional teams and manage external partnerships.
• Master of Science, PhD or equivalent coupled with previous project management experience.

Closing Date for Applications – 8th March 2026

Please take a copy of the Job Description, as this will not be available post closure of the advert. 

When applying for this role, please use the ‘cover letter’ of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you have provided in your cover letter and CV will be used to assess your application.

At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together.

Working Model and Location: This role is based in the United Kingdom. The role follows a hybrid working model. You will attend the office for collaboration and key meetings. You will work remotely for focused tasks as agreed with your manager.

#LI-GSK

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive.

We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.

We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.

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