Director Site Contracts & Budgets (remote)

BioNTech SECambridge, MA
50dRemote

About The Position

The Director, Clinical Trial Contracts and Budgets, is responsible for building and leading a high-performing team that manages the full lifecycle of clinical trial contract and budget escalations across our global portfolio. This role provides strategic direction, oversight, and management of the Clinical Trial Contracts and Budgets function, ensuring operational excellence and compliance with all relevant regulations. The Director will optimize processes, serve as the primary escalation point for contract and budget issues, and drive the development and lifecycle management of Master Clinical Trial Agreements (CTAs) and rate cards. This position collaborates closely with internal stakeholders including; Legal, Data Privacy, Global Regulatory Affairs, and external CRO partners to ensure timely, high-quality execution of clinical trial agreements and budget management, supporting BioNTech's mission to deliver transformative therapies.

Requirements

  • Bachelor's degree in life sciences, finance, business, or related field required; advanced degree (JD, MBA, MSc, or similar) preferred.
  • Minimum 12 years of experience in clinical research, with at least 5 years in clinical trial contract and budget negotiation/management in the US pharmaceutical, biotech, or CRO environment.
  • Minimum 5 years of direct line management experience, including responsibility for hiring, performance management, and team development.
  • Demonstrated success in people development, including coaching, mentoring, and building high-performing teams.
  • In-depth knowledge of US clinical trial regulations, contract law, and industry standards (FDA, ICH-GCP, Sunshine Act, etc.).
  • Proven ability to develop and implement standardized processes and drive operational excellence.
  • Strong financial and contract acumen.
  • Excellent communication, analytical, and critical thinking skills.
  • Proficiency with contract management and clinical trial management systems.
  • Demonstrated self-starter and team player with strong interpersonal skills.
  • Willingness to travel as required (less than 15%).

Nice To Haves

  • Experience with digital tools, automation, or process optimization in contract/budget management is a plus.

Responsibilities

  • Provide strategic leadership for the Clinical Trial Contracts and Budgets function, including resource planning, team development, and performance management.
  • Directly manage, coach, and develop team members, fostering a high-performance culture and supporting professional growth and talent retention.
  • Act as the subject matter expert and primary escalation point for all clinical trial contract and budget issues, ensuring timely and effective resolution of complex negotiations with CRO partners and clinical trial sites.
  • Lead the development, implementation, and lifecycle management of Master CTAs and rate cards, ensuring alignment with company standards, US regulations, and industry best practices.
  • Continuously improve and standardize processes, templates, and fallback language for contracts and budgets in collaboration with internal and external cross-functional stakeholders and strategic partners.
  • Drive operational excellence by identifying and implementing process improvements and automation opportunities to increase efficiency and reduce cycle times.
  • Monitor and analyze contract and budget performance metrics at the portfolio, trial, and site levels; proactively address risks and inefficiencies.
  • Ensure compliance with US and international regulations (e.g., FDA, ICH-GCP), company policies, and industry best practices.
  • Partner with internal and external stakeholders to develop and maintain strong working relationships, ensuring alignment and transparency throughout the contract and budget lifecycle.
  • Provide strategic input in translating protocol elements into efficient and feasible contract and budget development and traceable invoiceables.
  • Support internal and external audits, inspections, and due diligence activities as the subject matter expert for clinical trial contracts and budgets.
  • Develop and deliver training and guidance to team members and stakeholders on contract and budget processes, systems, and compliance requirements.

Benefits

  • Medical, Dental and Vision Insurance
  • Life, AD&D, Critical Illness Insurance
  • Pre-tax HSA & FSA, DCRA Spending Accounts
  • Employee Assistance & Concierge Program (EAP) available 24/7
  • Parental and Childbirth Leave & Family Planning Assistance
  • Sitterstream: Virtual Tutoring & Childcare Membership
  • Paid Time Off: Vacation, Sick, Bereavement, Holidays (including Floating) & Year-End U.S. Shutdown.
  • 401(K) Plan with Company Match
  • Tuition Reimbursement & Student Loan Assistance Programs
  • Wellbeing Incentive Platforms & Incentives
  • Professional Development Programs
  • Commuting Allowance and subsidized parking
  • Discounted Home, Auto & Pet Insurance

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What This Job Offers

Job Type

Full-time

Career Level

Director

Industry

Chemical Manufacturing

Number of Employees

1,001-5,000 employees

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