Sr. Clinical Trial Manager, Oncology

The Role The Senior Clinical Trial Manager (Sr. CTM) provides clinical trial oversight to the assigned clinical trial(s), which may be complex or high priority, and ensures deliverables are met in terms of quality, compliance and timing. Strong vendor management is critical for this role. The position may report to the Sr. Director, Clinical Operations, Oncology. This role may work collaboratively on one trial or across several trials to support clinical operations activities. What You’ll Do Perform day‑to‑day management and oversight of assigned clinical trial(s) to ensure deliverables are met in all phases of trial. Lead the Clinical Trial Team, and support other development teams as a Clinical Operations representative as required. Perform and document study‑level sponsor oversight of outsourced clinical activities. Communicate study status, cost and issues to ensure timely decision‑making by senior management. Initiate and manage study‑level timelines, including communication to internal and external team members on deliverables. Work closely with other supporting clinical operations team members, if applicable, to execute clinical studies. Draft and/or oversee the drafting of site materials including training, manuals and support documentation. Review clinical data to ensure timely entry and readiness for data review meetings. Perform periodic review of clinical data, quality metrics and study deviations. Manage trial feasibility process and oversee site feasibility/capability assessments in collaboration with the CRO and cross‑functional team. Review and provide clinical operations input into relevant clinical documents such as the protocol, investigator brochure, regulatory documents, clinical study reports and other documents and plans as appropriate. Review clinical monitoring reports to ensure timely completion and identification of issues. Ensure trial samples are ready to be sent to vendors in order to meet trial deliverables. Complete and maintain internal clinical trial metrics, dashboards and other internal updates. Ensure trial is conducted in accordance with Moderna and ICH/GCP standards including multiple regions in global trials. Participate in testing of clinical trial systems/databases (i.e. UAT). Manage invoice and budget tracking for individual studies and provide input into budget forecasting activities. May support additional clinical trial(s) in various capacities (e.g., unblinded clinical trial manager, regional clinical trial manager, etc.). Participate in clinical operations workstreams related to departmental and operating model related initiatives. Develop and maintain strong, collaborative relationships with key stakeholders within and external to Moderna. Strive for continuous improvement and more efficient ways of working in clinical development. Act as a role model for Moderna’s values. Basic Qualifications 5-7 years of experience in a clinical research and industry environment, including a minimum of 2+ years of independent trial management preferred. Bachelor’s degree required; Advanced degree preferred. Robust oncology experience required. Desirable: immuno‑oncology, high complexity such as CAR‑T. Solid understanding of drug development. Good project management skills. Good understanding of FDA and ICH GCP guidelines to ensure the appropriate conduct of clinical studies. Excellent verbal and written communication skills. Good organizational skills and attention to detail. Pay & Benefits Best‑in‑class healthcare coverage, plus voluntary benefit programs to support your unique needs. A holistic approach to well‑being, with access to fitness, mindfulness, and mental health support. Family planning benefits, including fertility, adoption, and surrogacy support. Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year‑end shutdown. Savings and investment opportunities to help you plan for the future. Location‑specific perks and extras. Salary range: $130,800.00 – $209,400.00. Eligible for an annual discretionary bonus, other incentive compensation, or equity award subject to company plan eligibility criteria and individual performance. Equal Opportunities Moderna is committed to equal employment opportunity and non‑discrimination for all employees and qualified applicants without regard to a person’s race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Export Control Notice This position may involve access to technology or data that is subject to U.S. export control laws, including the Export Administration Regulations (EAR). As such, employment is contingent upon the applicant’s ability to access export‑controlled information in accordance with U.S. law. Due to the nature of the work and regulatory requirements, only individuals who qualify as U.S. persons (citizens, permanent residents, asylees, or refugees) are eligible for this position. For this role Moderna is unable to sponsor non‑U.S. persons to apply for an export control license. Reasonable Accommodation Notice Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations team at View email address on click.appcast.io. #J-18808-Ljbffr