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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 prevent and treat disease with specialty medicines, vaccines and general medicines. We focus on the science of the immune system and advanced technologies, investing in four core 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 perform 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.

As a focused biopharma company, we discover, develop and deliver medicines and vaccines to create value for patients and shareholders. We are on track to make a positive impact on the health of 2.5 billion people by the end of the decade. In R&D, we combine the science of the immune system with advanced technologies to develop new medicines and vaccines that can help transform people’s lives. We focus on four areas – respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – where we have the strongest expertise and significant patient need remains. By developing differentiated medicines and vaccines across these areas, we can deliver patient benefit at scale and generate value for people, health systems, shareholders and society.

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Position Summary

This role within GCSD plays a pivotal part in driving the clinical operations of assigned studies, from Commit to Study Initiation (CSI) all the way through to study archiving. As a Global Study Manager (GSM), you'll take ownership of crafting robust, accelerated delivery plans that aim for top-tier performance—ensuring timelines, quality standards, and ambitious targets are consistently achieved.

Collaborating closely with the Global Study Lead (GSL), you'll contribute to the seamless end-to-end delivery of the clinical study. As the GSM, you will lead the Operational Working Group (for in-house studies) and actively participate as a key member of the Central Study Team (CST). This is a dynamic and impactful role designed for individuals driven to make a meaningful difference in clinical operations.

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

• GSM will be the Working Group (WG) Lead for Clinical Operations with accountability for the operational delivery of clinical study/studies to time, quality, and budget, company standards and scientific requirements, supporting decision-making at pace and leading study team to achieve overall study deliverables

• As Operational WG Lead, GSM is accountable for the following deliverables (to be adjusted accordingly for the STOM FSO model):

  Study Initiation Meeting

  Clinical Study Activity Plan

  Study Delivery Plan

  TMF Quality Strategy Document

  DCT Set Up

  Study Demographic and Diversity Plan

  Vendors Oversight Plan

  Results Dissemination Plan

  Investigator/CRA Meeting Set Up & associated training

  Expected Document List

  Recruitment Tracking

  Budget tracking eTMF filing and Vendor Set Up and Management

  Patient Engagement Activities

  CSDD KOM & template

  Safety Management plan

  Protocol Deviation Management Plan

  eTMF & vendor set-up

  Pharmacy Manual

• Supports assessment and selection of FSO vendors

• Accountable for holistic oversight of FSO vendors according to the FSO handbook

• Responsible for assessment and selection of other study vendors under GCSD responsibility in consultation with GSL

• Ensures compliance with ICH/GCP guidelines, all applicable laws and regulations, and GSK SOPs for assigned studies. understand study contribution to program/submission

• Balances risk/benefit to make decisions based on clear understanding of impact on the study and project

• Proactively and effectively identifies, oversees, and mitigates study risks

• Ensures appropriate stakeholder communication, including study status, expectations, risks and issues

• Accountable to operate within the study budget

• Effectively leads empowered matrix teams

• Implements innovative approaches to study delivery through external facing advances in technology and sciences and encourages others within matrix and line teams to seek innovative perspectives and develop solutions.

• Responsible for operational input into protocol and informed consent form development, and other key study documents.

• Leads and conducts investigator meetings and other study related meetings

• Leads quality efforts to ensure protocol compliance and continual inspection readiness for assigned studies

• Ensures data quality plans and end to end data cleaning is performed instream by the responsible line functions

• Ensures Clinical Study Report is delivered on time and supports GSK’s adherence to local regulatory guidance

• Oversees the activities of the countries participating in the study

• Provides support and coaching (where appropriate) to the SM

• Ambassadors in increasing utilization of AIML tools, driving automation of manual processes, finding efficiencies and more effective ways of working

• This role follows GSK’s Performance with Choice flexible‑working approach—balancing individual flexibility with team collaboration—and requires on‑site attendance 2–3 days per week to support core team activities and business needs. Candidates are required to live in proximity to a GSK hub.

Why You?
Basic Qualifications
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:

Education Requirements:

• Bachelor’s degree: life sciences or related discipline

• The role will require a good understanding of complex clinical development and regulatory processes.

Job Related Experience:

• In-depth experience in clinical research: study management, monitoring, data management

• Strong skills and experience in project management and tools

• Strong performer / executor of operational tasks with strong skills and experience in study delivery

• Experience of working across multiple types of study designs

• In depth knowledge of GCPs and ICH guidelines

• Excellent stakeholder management and communication skills (oral and written), outstanding interpersonal skills.

• Demonstrates leadership skills, promoting motivation and empowerment of others in order to accomplish individual, team and organizational objectives

• Strong understanding of the clinical study, drug development, sample management and other associated process and quality requirements, including ICH/GCP guidelines and SOPs

• Good project management skills (including scope, budget, timeline, and resource planning and management, and use of associated tools and support where available)

• Able to lead and work within teams and networks across functional and geographical boundaries; leads by example and promotes collaboration, effective communication and leadership in others

• Able to manage competing priorities, performance targets and project initiatives in a global environment

• Operational expertise in risk management and contingency planning

• Applies industry best practices to the design and execution of clinical studies to improve time and cost efficiency

• Demonstrates conceptual, analytical and critical thinking

• Effective at problem solving and conflict resolution

• Ability to manage change and uncertainty

• Ability to delegate tasks

• Demonstrates experience in multicultural settings (to reflect our external customers/clients [health authorities/patients] and diverse environments with respect to dynamics of human interaction (including working with remote teams)

• Demonstrates versatility and ability to adapt to working across multiple TAs

• Ability to think independently, analyze and solve problems systematically and creatively, and to take a risk-based approach.

#LI-Hybrid

In compliance with Ontario's provincial pay transparency legislation, this job posting includes a salary range to support equitable and informed hiring practices. The annual compensation for this role is CAD117,000 to CAD167,000 , determined based on experience, qualifications, and internal equity. GSK is dedicated to promoting transparency and fairness throughout our recruitment process.Salary ranges for other locations are shown because some markets have pay transparency laws that require salary information on job postings, and those locations are potential job sites for this role. If salary ranges are not displayed in the job posting for a specific location or country, the relevant compensation will be discussed during the recruitment process.

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. GSK is committed to accommodating persons with disabilities. If you need accommodation at any stage of the application process or want more information on our accommodation policies, please contact us at . Please do not send resumes to this e-mail and instead apply through the online application process of this posting.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK.