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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.

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