GlaxoSmithKline
Director Third Party Excellence
GlaxoSmithKline, Collegeville, Pennsylvania, United States, 19426
Position Summary
The Director, Third Party Excellence is responsible for ensuring successful delivery of GSK’s clinical studies by establishing and sustaining strong governance and strategic relationships with third‑party providers. This role drives compliance with contractual and regulatory requirements, oversees portfolio‑level performance against expectations, proactively identifies and mitigates risks and issues, and seeks opportunities to improve third‑party performance. The TP Director leads a multidisciplinary, cross‑functional oversight team in a matrix environment, partnering closely with functional and business stakeholders.
Responsibilities
Governance of key third parties delivering services across multiple functions.
Relationship management as primary contact within Global Clinical Operations and affiliated clinical development functions.
Cross‑therapeutic area full‑service provider oversight collaborating with the Research Unit Third Party Management Directors.
Drive efficient governance forums focusing on performance mitigation.
Translate information into key insights, identify risks and opportunities, and drive strategies and actions.
Senior escalation point, facilitate discussions with internal and external stakeholders to accelerate resolution.
Conduct internal and external operational cross‑portfolio reviews, partnership updates, feedback, and risk assessment.
Accountable for full portfolio of services delivered by assigned third parties, ensuring timely execution and adherence to MSA, SLA, and QAg.
Establish TP partnership KPIs, review KPIs, KQIs, and KFIs with third parties, analyze trends and propose strategies.
Ensure documentation for oversight, governance, risk management, issue resolution, and strategic discussions for audit readiness.
Robust oversight of third parties at the cross service level.
May contribute to functional and cross‑functional initiatives and improvement projects.
Basic Qualifications
Bachelor’s degree or equivalent in a relevant field.
Prior management and oversight of cross‑functional FSO or FSP providers delivering a range of services including clinical operations.
Experience in late‑phase Global Clinical Trial Management or Study Management gained in a pharmaceutical company or CRO.
Proven experience in third‑party management, vendor management, procurement or contracting.
Experience working in a regulated environment within pharmaceuticals, biotech, or healthcare.
Strong stakeholder management and influencing skills across functions and senior levels.
Demonstrable track record of leading matrix teams and delivering operational improvements.
Good analytical skills and experience using data to drive decisions and monitor supplier performance.
Preferred Qualifications
Master’s or professional qualification in a relevant field.
Experience implementing third‑party governance in large, matrixed organizations.
Familiarity with contract management systems, vendor risk platforms or procurement tools.
Knowledge of global regulatory frameworks and standards relevant to clinical research or manufacturing.
Experience working with CROs, clinical vendors, or multi‑country supplier networks.
Proven ability to lead change, simplify processes and deliver measurable cost or risk reductions.
Closing Date Applications closing Tuesday 13th January 2026.
Salary and Benefits The annual base salary in Poland for new hires in this position ranges from PLN 441,750 to PLN 736,250 gross.
Other benefits may include private healthcare, additional paid days off, life insurance, private pension plan and fully paid parental leave.
Equal Opportunity 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.
Additional Information Apply now to join us and help build safer, more effective partnerships that accelerate progress for patients.
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Responsibilities
Governance of key third parties delivering services across multiple functions.
Relationship management as primary contact within Global Clinical Operations and affiliated clinical development functions.
Cross‑therapeutic area full‑service provider oversight collaborating with the Research Unit Third Party Management Directors.
Drive efficient governance forums focusing on performance mitigation.
Translate information into key insights, identify risks and opportunities, and drive strategies and actions.
Senior escalation point, facilitate discussions with internal and external stakeholders to accelerate resolution.
Conduct internal and external operational cross‑portfolio reviews, partnership updates, feedback, and risk assessment.
Accountable for full portfolio of services delivered by assigned third parties, ensuring timely execution and adherence to MSA, SLA, and QAg.
Establish TP partnership KPIs, review KPIs, KQIs, and KFIs with third parties, analyze trends and propose strategies.
Ensure documentation for oversight, governance, risk management, issue resolution, and strategic discussions for audit readiness.
Robust oversight of third parties at the cross service level.
May contribute to functional and cross‑functional initiatives and improvement projects.
Basic Qualifications
Bachelor’s degree or equivalent in a relevant field.
Prior management and oversight of cross‑functional FSO or FSP providers delivering a range of services including clinical operations.
Experience in late‑phase Global Clinical Trial Management or Study Management gained in a pharmaceutical company or CRO.
Proven experience in third‑party management, vendor management, procurement or contracting.
Experience working in a regulated environment within pharmaceuticals, biotech, or healthcare.
Strong stakeholder management and influencing skills across functions and senior levels.
Demonstrable track record of leading matrix teams and delivering operational improvements.
Good analytical skills and experience using data to drive decisions and monitor supplier performance.
Preferred Qualifications
Master’s or professional qualification in a relevant field.
Experience implementing third‑party governance in large, matrixed organizations.
Familiarity with contract management systems, vendor risk platforms or procurement tools.
Knowledge of global regulatory frameworks and standards relevant to clinical research or manufacturing.
Experience working with CROs, clinical vendors, or multi‑country supplier networks.
Proven ability to lead change, simplify processes and deliver measurable cost or risk reductions.
Closing Date Applications closing Tuesday 13th January 2026.
Salary and Benefits The annual base salary in Poland for new hires in this position ranges from PLN 441,750 to PLN 736,250 gross.
Other benefits may include private healthcare, additional paid days off, life insurance, private pension plan and fully paid parental leave.
Equal Opportunity 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.
Additional Information Apply now to join us and help build safer, more effective partnerships that accelerate progress for patients.
#J-18808-Ljbffr