2026 Co-Op, Clinical Risk, Compliance, and TMF/Systems

Contribute and support continuous improvement initiatives in the Clinical Risk, Compliance, TMF & Systems space (e.g., AI projects) that will focus on evaluating and streamlining GCP processes and tools.,Support oversight of data and records in the Veeva eTMF and other applicable electronic data systems.,Partner with Clinical Compliance Leads and study team members to investigate and document GCP quality events.,Participate in GCP quality event data reviews to ensure consistency in documentation, identification of trends, and opportunities for continuous process improvement.,Support TMF Systems & Operations initiatives by assisting with configuration reviews, user access tracking, and documentation updates within Veeva Vault eTMF to help ensure inspection readiness and data integrity.,Partner with TMF Leads and TMF Systems team members to analyze TMF metrics and reports (e.g., completeness trends, timeliness dashboards) and identify opportunities for process improvement.,Support reconciliation or oversight activities by performing structured reviews of TMF artifacts/sub-artifacts against defined criteria under supervision, helping strengthen inspection readiness practices.,Accept candid feedback and seek opportunities for self-improvement.,Engage in various departmental activities and attend relevant meetings as required.

Currently enrolled as a student working towards a bachelor’s degree in a science focused program (i.e., Biology, Chemistry, Pharmacy) or similar.,At least 3 years of study in one of the above scientific fields preferred.,Basic familiarity with pharmaceutical regulations (GCP) is a strong plus.,Must possess excellent organizational skills and ability to manage multiple priorities.,Basic familiarity with Microsoft Excel, Word, PowerPoint, etc. is a plus.,Excellent verbal and written communication skills and the ability to interact professionally with a diverse group, executives, managers, and subject matter experts.,Willingness to learn, be mentored, and improve.,Ability to work independently and in collaborative team environments.,Ability to work in a fast-paced demanding environment.,Ability to prioritize based on shifting demands.,Ability to multitask and know when to ask for help.,Willing and able to relocate to Cambridge, MA for the co-op.

Bachelor's Degree (currently pursuing)

Must be available to work full-time and on-site in Cambridge, MA for the entire duration of the program. Candidates must already hold work authorization in the US and be able to maintain that status without the need for future sponsorship. This position may involve access to technology or data subject to U.S. export control laws; therefore, only U.S. persons (citizens, permanent residents, asylees, or refugees) are eligible. Moderna is unable to sponsor non-U.S. persons for an export control license for this role.