Job description
Site Name: Warsaw, Bengaluru Luxor North Tower, Italy - Siena, Mississauga Milverton Drive, Poznan Grunwaldzka, UK - Hertfordshire - Stevenage
Posted Date: Jan 27 2026
As Study Manager You will lead and coordinate the delivery of clinical and evidence generation studies from planning through close-out. You will work with study teams, vendors, and country colleagues to keep studies on time, on budget, and compliant with standards. We value clear communication, practical problem solving, and a focus on quality. This role offers growth through exposure to global study delivery, the chance to shape ways of working, and meaningful impact aligned with our mission of uniting science, technology and talent to get ahead of disease together.
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
* Monitor study conduct and progress; identify, resolve and escalate risks/issues.
* Draft and review key clinical documents (Protocol, ICF) and study plans.
* Coordinate meetings and collaboration with internal teams and external partners (CROs, vendors).
* Support GSM in CRO oversight and delivery of delegated activities.
* Serve as primary vendor contact for study-specific deliverables.
* Provide country-level oversight: recruitment, data completeness, deviations, regulatory compliance.
* Manage study communications: meetings, newsletters, action logs and team rosters.
* Oversee clinical supply and investigational product delivery; identify risks and propose mitigations.
* Ensure eTMF inspection readiness; maintain completeness and quality of study documentation.
* Oversee budget tracking, change orders and expenses; ensure alignment with agreements and escalate issues.
* Actively contributes to Study Leadership and Central Study Teams; foster team dynamics and change adoption.
Why You?
Working arrangement
This role is hybrid. You will be expected to work regularly from our office and collaborate with international colleagues.
Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals
* At least 3+ years of relevant work experience in a pharmaceutical/scientific environment.
* Knowledge of clinical trials, drug development process.
* Strong knowledge of ICH-GCP, clinical study delivery process, including regulations, operational best practices, industry standards. Well familiar with key systems used in clinical trial delivery. Experience in using Trial Master File industry accepted standard.
* Project management skills (preferably with analytical/financial skills) and good leadership skills.
* Excellent verbal and written communication in English.
* Strong knowledge of, and skills in applying, applicable clinical trial regulatory requirements, i.e. GCP and ICH guidelines.
* Ability to manage multiple competing priorities with leadership guidance across various clinical studies with good planning, time management and prioritization skills.
* Logical/analytical thinking and an inclination to spot patterns and outliers. Quality mindset, critical sense, attention to details, effective training and mentoring skills.
* Knowledge of project finance and accounting principles in order to understand budget, invoices, cross-charges and expense reports.
* Excellent comprehension of Microsoft Office tools and CTM systems.
* Good stakeholder management and communication skills (oral and written), strong interpersonal skills.
* Results driven and efficient
* Ability to adjust to work in cross-functional squads in the agile model.
What we offer:
* Performance with Choice – flexibility in working mode (hybrid working model 2/3 days per week in the office), flexible working hours.
* Established job in an international, well-known pharmaceutical company.
* Opportunity to work in professional team playing crucial role in maintaining GSK portfolio on the markets.
* Opportunity to work within GSK standards and documentation applied globally.
* Wide range of benefits (Medical Plan, Life Insurance, Employee Retirement Program, Sport and recreation cards, Recreation allowance, annual bonus).
* Supportive & friendly working environment.
We’re looking for someone who thrives in a collaborative environment, is passionate about delivering results, and is eager to make a difference. If this sounds like you, we’d love to hear from you!
#LI-GSK
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The annual base salary in Poland for new hires in this position ranges from PLN 186,750 to PLN 311,250 gross, taking into account a number of factors including the candidate’s skills, experience, education level and the market rate for the role. Depending on the role and internal policies, the position may also be eligible for a bonus (if applicable and based on defined, non-discretionary criteria) and/or awards for exceptional performance (granted at the employer’s discretion). All statutory benefits will be maintained in accordance with Polish law. Other benefits may also be offered, which may include private healthcare, additional paid days off, life insurance, private pension plan and fully paid parental leave & care of family member leave.
More detailed information on the total reward package applicable to your role will be supplied during the 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. Please note salaries vary by country based on the market rate for the role.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 CAD91,000 to CAD141,000, 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.
As an Inclusive employer, we encourage you to reach out if you need any adjustments during the recruitment process. Please contact our Recruitment Team at pl.recruitment-adjustments@gsk.com to discuss your needs.
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.
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