Associate Director, Associate Clinical Operations Asset Lead

Questa posizione è in GSK

Il processo di selezione sarà interamente gestito GSK.

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Business Introduction 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. Find out more: (Our approach to R&D)(#)

Position Summary

You will support and lead operational delivery for complex oncology late clinical assets. You will work closely with EDT/MDT, Study Team and COAL to keep studies inspection ready and deliver high-quality, regulatory-grade data. We value clear decision making, collaborative leadership, and practical problem solving. This role offers strong growth, the chance to influence program strategy, and the opportunity to help GSK unite science, technology and talent to get ahead of disease together.

Key Responsibilities

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

• Lead and support the operational strategy and delivery for assigned late phase development streams, ensuring alignment with the clinical development plan.
• Coordinate cross-functional inputs from clinical, biostatistics, safety, clinical supplies and vendors to meet timelines and quality expectations.
• Represent DevOps at EDT/MDT.
• Contribute to protocol development, operational feasibility assessments and resourcing decisions, including insourcing versus outsourcing recommendations.
• Maintain inspection readiness and quality oversight, supporting risk management, mitigation plans and serious breach escalation when needed.
• Provide operational input for regulatory deliverables and governance forums, including scenario modelling and budget forecasting for clinical activities.
• Act as a point of contact for stakeholders and vendors to ensure consistent execution across studies and sub-projects.

Why You?

Basic Qualification

We are seeking professionals with the following required skills and qualifications to help us achieve our goals

• Bachelor’s degree in life sciences, health sciences or equivalent qualification.
• Experience in oncology clinical development.
• Experience in vendor management and oversight of Contract Research Organization (CRO) relationships.
• Experience working in roles requiring application of Good Clinical Practice (GCP) and clinical development processes
• Experience delivering global study oversight across multiple regions.

Preferred Qualification

If you have the following characteristics, it would be a plus

• Experience managing multiple stakeholders and communicating in written and verbal English in a professional setting.
• Experience in Phase II-III programs.
• Working on complex, multi-indication programs.
• Experience in clinical operations, clinical project or program management.
• Experience contributing to regulatory submission content or supporting regulatory interactions.
• Experience with budgeting and forecasting for clinical studies.
• Familiarity with clinical supplies, bio-sample management or diagnostic implementation.
• Experience working in matrix teams and mentoring junior colleagues.

Working model This role is hybrid. You will typically work 2 to 3 days per week onsite at a GSK office. #GSK-LI

Skills

Analytical Thinking, Clinical Data Interpretation, Clinical Data Review, Clinical Development, Clinical Trial Designs, Clinical Trials Monitoring, Cross-Departmental Collaboration, Digital Fluency, Drug Regulatory Affairs, Executive Presence, Hematology and Oncology, Learning Agility, Matrix Leadership, Scientific Presentations Polish Salary Range / Polski przedział wynagrodzenia: PLN 373,500 to PLN 622,500 Italian Salary Range / Fascia retributiva in Italia: EUR 66,000 to EUR 110,000 The annual gross base salary range for new hires in this position is listed above for each applicable location. These ranges take into