RTSM Project Manager (Clinical Trials)
Remote | Contract | $80–95/hour W2
About the Role
We are seeking an experienced RTSM Project Manager to support global clinical trials by leading the design, configuration, validation, and implementation of studies within a Randomization and Trial Supply Management (RTSM/IRT) platform. This role partners with Clinical Operations, Clinical Supply, Data Management, Biostatistics, and other cross-functional teams to ensure study requirements are accurately translated into validated RTSM solutions.
Responsibilities
- Lead end-to-end RTSM study design and implementation.
- Translate clinical protocols into RTSM system configurations.
- Configure randomization and clinical trial supply strategies.
- Coordinate User Acceptance Testing (UAT) and study validation.
- Support protocol amendments and study updates.
- Develop user guides and system documentation.
- Ensure study readiness prior to production go-live.
- Collaborate with cross-functional clinical teams throughout the study lifecycle.
Qualifications
- Bachelor's degree in Life Sciences, Computer Science, or related field.
- 3+ years of hands-on RTSM/IRT experience.
- Experience configuring and managing clinical trial studies.
- Knowledge of randomization methodologies and clinical supply management.
- Experience supporting GxP regulated systems.
- Strong documentation and stakeholder management skills.
- Experience with RAMOS preferred; experience with other enterprise RTSM/IRT platforms is acceptable.