Head of RTSM (Randomization and Trial Supply Management)

Head of RTSM (Randomization and Trial Supply Management) GlaxoSmithKline United States, Pennsylvania, Collegeville 1250 South Collegeville Road (Show on map) May 09, 2026

Site Name:

USA

• Pennsylvania
• Upper Providence, UK
• Hertfordshire
• Stevenage

Posted Date:

May 8 2026 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 lead the RTSM (Randomization and Trial Supply Management) function in the United States. You will partner with clinical development, operations, quality and external vendors to design and deliver patient-focused randomization and clinical supply solutions. We value clear decision-making, pragmatic problem solving, and inclusive leadership. You will shape strategy, build capability, and drive consistent delivery for clinical studies. This role offers strong growth, real impact on patients, and the chance to work where science, technology and talent come together to get ahead of disease. Responsibilities This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

• Lead design and delivery of RTSM strategies across Phase I-IV clinical programs and investigator-sponsored studies.
• Direct cross-functional teams and vendors to ensure on-time randomization, kit assignment, and clinical supply availability to sites and patients.
• Own risk assessments and contingency plans for trial supply and randomization activities.
• Establish and improve RTSM processes, metrics, and governance to drive quality and efficiency.
• Partner with clinical operations, biostatistics, data management, and regulatory functions to align RTSM with study design and compliance needs.
• Hire, coach and develop a diverse team, and foster collaboration across internal and external partners.

Why You?

Basic Qualifications:

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

• Bachelor's degree in life sciences, pharmacy, engineering, IT, or related field, or equivalent experience.
• 8+ years of experience managing RTSM, IRT, or clinical supply systems in the pharmaceutical or biotech industry.
• Experience leading cross-functional teams and managing external vendor relationships.
• Experience with clinical trial operations, randomization methods, blinding and investigational product supply principles.
• Experience with system vendor selection, implementation, validation, and change control.

Preferred Qualifications:

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

• Advanced degree in a relevant discipline or equivalent senior leadership experience.
• Experience with eClinical ecosystems, integrations between RTSM and clinical systems, and data flows.
• Background in global trial support and managing multi-region supply and regulatory requirements.
• Proven track record of building and mentoring high-performing teams.
• Experience implementing process improvements, metrics and dashboards to measure RTSM performance.
• Knowledge of relevant regulations and GxP expectations for clinical supply and systems.
• Clear communication skills with experience presenting to senior stakeholders and managing escalations.

Work Model This role is hybrid. You will be expected to be on-site regularly and collaborate across sites and with global colleagues. #GSK-LI Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees. 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. If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at

• usrecruitment.

adjustments@gsk.com 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. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of

GSK. GSK

shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/