- Accountable for the strategic leadership and delivery of clinical study/studies to time, quality, and budget, company standards and scientific requirements, driving decision‑making at pace and strategically leading study team to achieve overall study deliverables.
- Effectively build and lead empowered, high‑performing global matrix teams.
- Provide Oncology therapeutic area expertise to support operations.
- Translate strategic concepts, stakeholder feedback and requirements into cohesive actions for the study team.
- Ensure compliance with ICH/GCP guidelines, all applicable laws and regulations.
- Ensure appropriate stakeholder communication, including study status, expectations, risks and issues and influence / manage stakeholders at senior director and/or VP level.
- Ensure robustness in upfront feasibility and planning.
- Accountable for the study budget as well as preparation of materials for governance and/or financial review cycles.
- Oversee quality efforts to ensure protocol compliance and continual inspection readiness for assigned studies.
- Lead assessment, selection, oversight and issue management for FSO vendors.
- Optimize utilization of digital and tech tools such as AIML to find efficiencies and more effective ways of working.
- Bachelor's degree in life sciences, health science, nursing, pharmacy, or related field.
- Extensive clinical development experience (5+ years) and proven experience in driving operational study delivery to time, cost, and quality within the pharmaceutical industry or CRO environment.
- Significant experience leading complex, global Oncology studies.
- Proven experience working with investigators, external experts, and oversight of Contract Research Organizations and third‑party vendors.
- Strong knowledge of ICH Good Clinical Practice and global regulatory requirements.
- Proven project and budget management skills with evidence of delivering to timelines and quality targets.
- Proven depth and breadth of experience in clinical delivery, across indications, assets, phases, regions, etc.
- Preferred Qualification
- Postgraduate degree in a life science, clinical research, or project management field.
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Site Name: Mississauga Milverton Drive, Bangalore, Belgium-Wavre, Italy - Siena, UK - Hertfordshire - Stevenage, USA - Pennsylvania - Upper Providence, Warsaw Rzymowskiego 53 · Posted Date: Feb · Position Summary · As Global Study Lead (GSL) you will lead the operational deliver ...
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Site Name: · Mississauga Milverton Drive, Bangalore, Belgium-Wavre, Italy - Siena, UK - Hertfordshire - Stevenage, USA - Pennsylvania - Upper Providence, Warsaw Rzymowskiego 53 · Posted Date: · Feb · *Position Summary · As Global Study Lead (GSL) you will lead the operational de ...
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Nazwa biura: Mississauga Milverton Drive, Bangalore, Belgium-Wavre, Italy - Siena, UK - Hertfordshire - Stevenage, USA - Pennsylvania - Upper Providence, Warsaw Rzymowskiego 53 · Posted Date: Feb · Position Summary · As Global Study Lead (GSL) you will lead the operational deliv ...
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This role within GCSD plays a pivotal part in driving the clinical operations of assigned studies. · Please see below for key responsibilitiesGSM will be the Working Group (WG) Lead for Clinical Operations with accountability for operational delivery. · GSM is accountable for hol ...
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This role within GCSD plays a pivotal part in driving the clinical operations of assigned studies. · As a Global Study Manager (GSM), you'll take ownership of crafting robust delivery plans that aim for top-tier performance—ensuring timelines, quality standards, and ambitious tar ...
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Global Study Lead - Siena - GlaxoSmithKline
Descrizione
Posted Date: Feb
Position Summary
As Global Study Lead (GSL) you will lead the operational delivery of complex global clinical studies from study initiation through archiving. You will work with cross‑functional and external partners to set clear study plans, manage risk, and deliver against time, quality and budget goals. We value strategic leaders who are pragmatic, collaborative, and focused on patient‑centered outcomes. This role offers strong opportunities for growth, visible impact on clinical development, and the chance to contribute to GSK's mission of uniting science, technology and talent to get ahead of disease together.
Key Responsibilities
Why This Role?
This is a hybrid role based in GSK HUB locations with an expectation to be in the office 2–3 days per week.
Basic Qualifications
Compensation & Benefits
The annual base salary in Poland for new hires in this position ranges from PLN 339,750 to PLN 566,250 gross, depending on skills, experience, education level and market rate for the role. The position may also be eligible for a bonus (if applicable) and/or awards for exceptional performance.
Other statutory benefits will be maintained in accordance with Polish law. Other benefits may also be offered, including private healthcare, additional paid days off, life insurance, private pension plan and fully paid parental leave & care of family member leave.
About GSK
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.
Inclusion
As an employer committed to Inclusion, we encourage you to reach out if you need any adjustments during the recruitment process.
Please contact our Recruitment Team at IN.recruitment- to discuss your needs.
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