Associate Director, Trial Operations & Budget

AdvanCell; Boston (MA); On-site; USD 150,000 - 190,000; Full time

Job summary

AdvanCell seeks an Associate Director, Trial Operations & Budget to lead oversight, planning and execution of clinical trial activities with a focus on financial stewardship. You will collaborate with CROs, vendors and clinical sites to manage budgets, contracts, invoicing and TMF quality in line with SOPs, protocols and ICH/GCP.

Reporting to the VP of Clinical Development and Operations, you will drive vendor management, change control and performance metrics across global studies, ensuring

Qualifications

• Bachelor’s degree in life sciences; MSc or higher preferred.
• Strong knowledge of ICH-GCP guidelines and regulatory requirements.
• Experience budgeting, forecasting, and financial reconciliation in clinical operations.
• Exposure to TMF processes and inspection readiness.

Responsibilities

• Develop, manage, and track site and study budgets with CROs and internal Finance.
• Review, reconcile, and approve vendor and CRO invoices against contracts and milestones.
• Support contracting processes including review of scopes of work and amendments.
• Manage change orders, timelines, and budget alignment.
• Generate and maintain purchase orders per study budgets.
• Support vendor onboarding and performance management to meet KPIs.
• Oversee CROs to ensure studies meet timelines and quality standards.
• Ensure TMF quality and completeness for inspections.

Skills

Budget management

Forecasting

Financial reconciliation

Vendor management

ICH-GCP knowledge

Cross-timezone collaboration

Attention to detail

Education

Bachelor's in Life Sciences

MSc or higher preferred

Tools

CTMS

eTMF

Job description

The Associate Director, Trial Operations & Budget is responsible for supporting the oversight, planning, and execution of clinical trial activities, with a strong emphasis on financial management and operational excellence. This role ensures that clinical operations deliverables related to CROs, vendors, and clinical sites management and oversight, including budgeting, contracting, invoicing, and Trial Master File (TMF) quality and completeness verification—are conducted in alignment with corporate financial and clinical operations SOPs, study protocols, ICH/GCP guidelines, regulatory requirements, and established budget and timelines. Reporting to the VP, Clinical Development and Operations, this position plays a critical role in vendor management, financial stewardship, and the delivery of high-quality, efficient clinical trials.

Key Responsibilities and Duties

Responsibilities will include, but not limited to:

• Develop, manage, and track site and study budgets in collaboration with CROs and internal Finance partners.
• Review, reconcile, and approve vendor and CRO invoices against contracts, milestones, and deliverables.
• Support clinical operations contracting processes, including review of scopes of work, vendor agreements, and amendments.
• Manage and review change orders, ensuring alignment with scope, timelines, and budget.
• Generate andmaintainpurchase orders (POs)in accordance withcompany processes and study budgets.
• Support vendor selection, onboarding, and ongoing performance management to ensure adherence to KPIs and contractual commitments.
• Support oversight of CROs to ensure clinical trials are executed according to timelines, quality standards, and contractual obligations.
• Conduct and/or oversee quality control of the Trial Master File (TMF) to maintain accuracy and continuous inspection readiness. Monitor TMF completion metrics to ensure timely and comprehensive document completeness.
• Collaborate closely with cross-functional teams including Finance, Legal, CMC, Pre-clinical to ensure seamless execution of clinical programs.
• Proactively identify risks in study execution and financial management, and implement mitigation strategies.
• Support onboarding procedure and training on internal processes for new team members.

Other Responsibilities

• Adhere to the Company’s quality management system processes and policies.
• Comply with applicable regulatory requirements, policies, and procedures related to financial reporting transparency, Good Clinical Practice (GCP), and Good Documentation Practice (GDP).
• Other tasks as requested by the VP Clinical Development and Operations.

Essential Skills, Qualifications, Industry and Educational Requirements

• Strong knowledge of clinical trial conduct, ICH-GCP guidelines, regulatory requirements, and the Sunshine Act.
• Meticulous attention to detail to ensure accuracy in documentation and financial tracking.
• Demonstrated ability to manage budgets, forecasting, and financial reconciliation.
• Flexibility to collaborate across different time zones
• Experience with TMF processes andinspectionreadiness standards.
• Ability to worktotimelines and perform effectively in high-pressure environments.
• Strong organizational, analytical, and problem-solving skills.

Desirable Skills, Qualifications, Industry and Educational Requirements

• Proventrack recordin clinical operations delivery within a sponsor or CRO environment.
• Demonstratedexpertisein vendor management, CRO oversight, and contract management.
• Experience with budgeting tools, CTMS, and eTMF systems.
• Strong communicationand collaboration skills across cross-functional teams.
• Minimum 6–10 years’ experience in clinical operations (depending on level).
• Bachelor’s degree in life sciences required; advanced degree (MSc or higher) preferred.