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Decision details from the source listing
Bachelor's degree in Life Sciences or related discipline
authorization to work in Poland
fixed
Standard (Mon-Fri)
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What this posting tells you
Senior Global Study Lead position providing end-to-end leadership for complex global clinical studies with remote work possible in Poland. Requires extensive experience in clinical operations, team leadership, regulatory compliance, study budgeting, and CRO management. Work schedule is standard Monday to Friday, office environment noted. Bachelor’s degree in Life Sciences or related field required. No salary range specified.
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Poland
Europe/Warsaw
senior · full_time
- Compensation is not listed
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Explore the remote job marketGlobal Study Lead - FSP EMEA at REGON 011115826 PPD Poland Sp. Z o.o
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
The Opportunity
We are seeking an experienced Global Study Lead (GSL) to provide strategic and operational leadership for complex global clinical studies.
This is a senior study leadership position with end-to-end accountability for clinical study delivery, from study initiation through to study close-out and archiving. You will define the operational strategy, lead cross-functional study teams, and ensure studies are delivered to the required timelines, quality, budget and regulatory standards.
As a key member of the Study Leadership Team, you will represent Clinical Operations and work closely with Clinical, Statistics and other cross-functional partners to drive decisions, manage risk and ensure successful study delivery.
Key Responsibilities
- Lead the operational strategy and end-to-end delivery of one or more global clinical studies.
- Own study timelines, budget, quality, risks and key operational deliverables.
- Provide strategic leadership to global, cross-functional study teams and drive timely decision-making.
- Represent Clinical Operations within the Study Leadership Team and act as the senior escalation point for operational issues.
- Translate clinical development and asset strategy into clear study-level operational plans.
- Lead proactive study risk identification, mitigation and issue resolution.
- Ensure robust feasibility, study planning and operational execution.
- Provide strategic operational input into protocols, informed consent forms and other key study documents.
- Oversee CROs and other external vendors, including vendor selection, performance management and escalation where deliverables are at risk.
- Ensure studies remain compliant with ICH-GCP, applicable regulations, SOPs and inspection-readiness requirements.
- Lead study financial planning, forecasting and budget management.
- Communicate study progress, risks, decisions and recommendations effectively to senior stakeholders and governance forums.
- Champion innovative approaches to clinical trial delivery, including decentralised trial approaches, technology, automation and AI-enabled ways of working.
- Contribute to continuous improvement initiatives across Clinical Operations.
About You
You will be an accomplished clinical operations professional with significant experience leading complex global clinical studies within the pharmaceutical or biotechnology industry.
You will bring
- A Bachelor's degree in Life Sciences or a related discipline.
- Extensive experience in global clinical study delivery, ideally across multiple phases, indications and geographic regions.
- Proven experience holding end-to-end accountability for complex global clinical trials.
- Strong experience leading global cross-functional teams within a matrix environment.
- Demonstrated ownership of study timelines, budgets, risks, quality and operational strategy.
- Significant experience overseeing CROs and third-party vendors, including performance management and issue resolution.
- In-depth knowledge of ICH-GCP, global regulatory requirements and clinical development processes.
- Strong project and financial management capabilities.
- The ability to influence senior stakeholders and drive decisions in complex, fast-paced environments.
- Excellent leadership, communication, negotiation and conflict-management skills.
- Experience proactively identifying and resolving risks that could impact clinical programmes.
Highly Desirable
Experience in one or more of the following would be particularly valuable:
- Phase II and/or Phase III global clinical trials.
- Adaptive or other innovative trial designs.
- Decentralised clinical trials (DCTs).
- Platform, umbrella or basket studies.
- Technology-enabled clinical trial delivery, automation or AI/ML.
- Working with investigators, external experts and regulatory authorities.
- Broad therapeutic-area experience, combined with deep expertise in one or more indications.
What Success Looks Like
The successful Global Study Lead will be able to set the vision for study delivery, translate strategy into execution and bring diverse stakeholders together around clear priorities. You will be comfortable making complex decisions autonomously, challenging constructively, escalating when required and empowering teams to deliver in demanding global clinical-development environments.
Working remotely at REGON 011115826 PPD Poland Sp. Z o.o
REGON 011115826 PPD Poland Sp. Z o.o is hiring for 2 active remote roles, with remote-friendly openings, application links, and job details refreshed from the public remote job inventory.
Remote hiring signal is inferred from active confirmed-remote job listings.