Associate Director - Trial Operations & Budget

Salary Range: 170000 to 220000 (Currency: USD) (Pay period: per-year-salary)

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 and maintain purchase orders (POs) in accordance with company 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 and inspection readiness standards. 
Ability to work to timelines and perform effectively in high-pressure environments. 
Strong organizational, analytical, and problem-solving skills. 

Desirable Skills, Qualifications, Industry and Educational Requirements

Proven track record in clinical operations delivery within a sponsor or CRO environment. 
Demonstrated expertise in vendor management, CRO oversight, and contract management. 
Experience with budgeting tools, CTMS, and eTMF systems. 
Strong communication and 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.