Moderna
Sr. Clinical Trial Manager, Oncology
Cambridge, Massachusetts, USA · Senior · Contract
No sponsorship$131k-$209kDetected 28 days ago
GCPProject ManagementForecastingVendor ManagementClinical TrialsClinical ResearchFDA RegulatoryResearchCommunicationCollaborationOrganizational Skills
About the role
- 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. external vendors and CROs.
- Director, Clinical Operations, Oncology.
Responsibilities
- This role may work collaboratively on one trial or across several trials to support clinical operations activities.
- Initiate and manage study-level timelines, including communication to internal and external team members on deliverables
- Draft and/or oversee the drafting of site materials including training, manuals and support documentation
- Manage trial feasibility process and oversee site feasibility/capability assessments in collaboration with the CRO and cross-functional team
- Complete and maintain internal clinical trial metrics, dashboards and other internal updates
- 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
Nice to have
- Lead the Clinical Trial Team, and support other development teams as a Clinical Operations representative as required
- Communicate study-status, cost and issues to ensure timely decision-making by senior management
- Work closely with other supporting clinical operations team members, if applicable, to execute clinical studies
- Review clinical data to ensure timely entry and readiness for data review meetings
- 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
Skills
- Participate in testing of clinical trial systems/databases (i.e. UAT)
Compensation
- The salary range for this role is $130,800.00 - $209,400.00.
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
- Location-specific perks and extras
Visa & Work Authorization
- Perform and document study level Sponsor Oversight of outsourced clinical activities
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This listing is sourced directly from Moderna's careers page and normalized into a canonical job model.