RTSM Project Manager (Randomisation and Trial Supply Management)
About The Position
The Core-Tech RTSM team, part of GSK’s R&D Medicine Development and Supply division, manages key components for GSK’s clinical trial process using RTSM (IRT) to achieve R&D objectives. The RTSM Project Manager is responsible for the entire lifecycle of clinical studies within the RAMOS IRT system, including design, development, testing, validation, execution, and maintenance. This role also involves overseeing clinical studies managed by non-GSK IRT Vendors, ensuring data integrity, and driving continuous improvement across Clinical Supplies systems. The position requires acting as a key interface with internal and external stakeholders and suppliers, and may include direct line-management responsibilities.
Requirements
- Relevant Degree (e.g.; Science, Supply Chain, Technical, etc).
- Experience / Knowledge of clinical supplies/trials (including IRT knowledge/experience).
- Experience of managing projects.
- Understanding / knowledge of project governance and escalation processes including senior stakeholder communication and reporting.
Nice To Haves
- Business Data Mining
- Data Analysis
- Data Analysis Tools
- Data Mining
- Data Modeling
- Data Storytelling
- SQL Databases
- Statistical Analysis
- Structured Query Language (SQL)
Responsibilities
- Assess planned clinical trial studies for suitability for RAMOS IRT system, and independently configure and manage complex IRT study designs (including international or more complex / adaptive designs).
- Act as IRT group business point of contact for technical systems (Randomization and Container Code, Packaging, and Shipping Systems).
- Accountable for identifying, owning, and implementing process improvements and training needs & gaps.
- Proactively identify and communicate issues as well as proposing solutions.
- Raise Deviations/Customer Complaints and associated CAPAs.
- Draft, amend and determine gaps in SOPs.
- Lead interactions with RDIT for operational system issues and drive future IRT enhancements.
- Analyze data and drive/implement continuous improvements.
- Provide technical guidance/support to Clinical Development for their outsourced IRT studies.
- Develop supply strategy to eliminate stockouts, minimize waste and reduce shipments.
- Assist with Helpdesk during daytime hours and participate on Helpdesk Stand-by/On-Call rotations (nights, weekends, holidays).
Benefits
- Annual bonus
- Eligibility to participate in share-based long-term incentive program
- Health care and other insurance benefits (for employee and family)
- Retirement benefits
- Paid holidays
- Vacation
- Paid caregiver/parental and medical leave
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Mid Level
