About Aura Biosciences
Aura Biosciences is a clinical-stage biotechnology company developing bel-sar, a potentially transformative, first-in-class therapy for patients living with ocular cancers. Bel-sar represents an entirely novel approach to treating ocular cancers via its dual mechanisms of action of acute tumor necrosis and secondary anti-tumor immune activation. The Phase 3 registration study of Bel-sar in early choroidal melanoma, the largest patient segment of uveal melanoma, is fully enrolled, and earlier stage studies in metastases to the choroid and cancers of the ocular surface are ongoing. Aura's mission is to improve outcomes for patients living with ocular cancers by delivering a therapy that not only arrests tumor growth but also preserves vision and quality of life.
For more information, visit aurabiosciences.com. Follow us on X, @AuraBiosciences, and visit us on LinkedIn.
Position Summary
Aura Biosciences is the world's preeminent ocular oncology company. We are leveraging a novel targeted oncology platform to develop a potential new standard of care with a focus on ocular oncology.
We are looking to expand our Clinical Development Operations (CDO) team with this newly created position of Senior Manager, Trial Master File (TMF). The Senior Manager, Trial Master File (TMF) is responsible for the strategic oversight, governance, and quality of Aura Biosciences Trial Master Files across the company's clinical trial portfolio. This role ensures that TMFs — whether managed in-house or by CRO partners — are complete, inspection-ready, and maintained in compliance with ICH-GCP, applicable regulatory requirements, and internal SOPs throughout the trial lifecycle. The Senior Manager acts as the subject matter expert (SME) for TMF processes, systems, and standards, partnering closely with Clinical Operations, Regulatory Affairs, Quality Assurance, and external vendors.
Key Responsibilities
TMF Strategy & Governance
- Establish and maintain TMF governance standards, including the Reference Model, filing structure, and metadata conventions.
- Develop and maintain TMF-related SOPs, work instructions, and plans (e.g., TMF Management Plan) in alignment with ICH-GCP E6(R2/R3) and applicable regulations.
- Serve as the primary point of accountability for TMF inspection readiness across all active and archived studies.
Study-Level Oversight
- Provide TMF oversight for assigned studies, ensuring timely, accurate, and complete filing of essential documents.
- Conduct or oversee periodic TMF completeness and quality reviews; track and drive resolution of misfiled, missing, or duplicate documents.
- Partner with Clinical Trial Managers/CRAs to ensure real-time filing practices are followed by site- and study-level teams.
- Lead TMF reconciliation activities at key milestones (e.g., database lock, study closeout, filing of final study report).
Vendor & CRO Management
- Manage relationships with CRO and eTMF vendor partners; oversee TMF-related deliverables in outsourcing agreements and vendor oversight plans.
- Review and approve CRO TMF plans, transfer plans, and TMF health metrics/KPIs.
- Lead TMF reconciliation and document transfer activities when transitioning studies between vendors or bringing studies in-house.
Systems & Technology
- Serve as business owner or SME for the eTMF system (Veeva Vault), including configuration, user access, and system enhancements.
- Partner with IT/Digital Quality on system validation, upgrades, and integrations (e.g., CTMS-eTMF integration).
- Develop and deliver eTMF user training for internal staff and site-facing teams.
Inspection Readiness & Quality
- Ensure TMFs are audit- and inspection-ready at all times; support regulatory inspections (FDA, EMA, MHRA, etc.) and internal/external audits by preparing TMF documentation and responding to findings.
- Monitor and report TMF health metrics (completeness, timeliness, quality) to clinical operations leadership and study teams.
- Support CAPA development and implementation for TMF-related audit/inspection findings.
Leadership & Collaboration
- Line-manage and/or mentor TMF Specialists/Coordinators, if applicable, including performance management and development planning.
- Collaborate cross-functionally with Clinical Operations, Regulatory, Biostatistics, Data Management, Pharmacovigilance, and Quality Assurance to ensure alignment on document and records management practices.
- Represent TMF function in study team meetings, vendor governance meetings, and process improvement initiatives.
Qualifications
Education
- Bachelor's degree in life sciences, healthcare, business, or related field required; advanced degree a plus.
Experience
- 7+ years of clinical research experience, with a minimum of 4–5 years focused specifically on Trial Master File management, clinical document/records management, or clinical operations.
- Demonstrated experience with eTMF systems (e.g., Veeva Vault, Montrium, Phlexglobal, Ennov) required.
- Prior experience overseeing CRO-managed TMFs and vendor governance strongly preferred.
- Experience supporting regulatory inspections (FDA, EMA, or other health authorities) preferred.
- Prior people management or mentorship experience a plus.
Knowledge & Skills
- Strong working knowledge of ICH-GCP E6(R2/R3), DIA TMF Reference Model, and applicable global regulatory requirements (FDA, EMA, ICH).
- Deep understanding of pharmaceutical and device clinical trial lifecycles and the essential documents required at each stage
- Excellent organizational, analytical, and problem-solving skills with strong attention to detail.
- Strong written and verbal communication skills; able to present TMF metrics and risks to senior leadership.
- Ability to manage multiple studies/priorities simultaneously in a fast-paced environment.
- Proficiency with Microsoft Office (Excel, PowerPoint) and clinical systems (CTMS, eTMF, EDC awareness).
Working Conditions
- Remote/hybrid or onsite
- Occasional travel (~20%) for CRO/vendor meetings, audits, or inspections.
Salary & Benefit Information
Salary Range: $150,000/yr - $185,000/yr
(Placement within the listed range depends on many factors including, but not limited to: geographic location, degree, years of experience, and internal company equity)
Health insurance with FULL premium coverage
401K with company match
Employee Stock Purchase Program (ESPP)
Competitive paid time off (PTO)
Company-paid short & long-term disability insurance and life insurance
Skills Required
- Bachelor's degree in life sciences, healthcare, business, or a related field
- At least 7 years of clinical research experience
- At least 4 to 5 years focused on Trial Master File management, clinical document or records management, or clinical operations
- Demonstrated experience with eTMF systems such as Veeva Vault, Montrium, Phlexglobal, or Ennov
- Working knowledge of ICH-GCP E6(R2/R3), the DIA TMF Reference Model, and applicable global regulatory requirements
- Understanding of pharmaceutical and device clinical trial lifecycles and essential documents
- Strong organizational, analytical, problem-solving, communication, and attention-to-detail skills
- Ability to manage multiple studies and priorities in a fast-paced environment
- Proficiency with Microsoft Office, including Excel and PowerPoint, and awareness of CTMS, eTMF, and EDC systems
- Advanced degree in a relevant field
- Experience overseeing CRO-managed TMFs and vendor governance
- Experience supporting FDA, EMA, or other health-authority regulatory inspections
- Prior people management or mentorship experience
What We Do
Aura Biosciences is a clinical-stage biotechnology company focused on developing precision therapies for solid tumors that aim to preserve organ function. Our lead candidate, bel-sar (AU-011), is currently in late-stage development for early choroidal melanoma and in early-stage development in other ocular oncology indications and bladder cancer. Aura Biosciences is headquartered in Boston, MA. Our mission is to grow as an innovative global oncology company that positively transforms the lives of patients.
