Revolution Medicines · 14 hours ago
Associate Director, EX US Clinical Site Contracts
Redwood City, California, United States
Contract
Onsite
Lead/Staff, Director/Executive
$186K/yr - $233K/yr
10+ years expRevolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies for RAS-addicted cancers. They are seeking a motivated Associate Director of Global Site Contracts responsible for managing EX US contracts and budget escalations while collaborating with stakeholders to support timely contract execution and site activation strategies.
Health CareLife ScienceMedical
Responsibilities
Understanding of the overall clinical development paradigm, especially around clinical study operations and have global or regional experience
Assume the management and oversight of direct reports, as well as any other duties that are deemed a need of the business
Effectively work with the legal and finance teams as well as external partners to ensure clinical agreements comply with the business’s best practices and relevant country regulations
Ensure all deliverables of the site contracts group are aligned with defined study timelines provided by the clinical operations team
Ensure team’s work complies with established practices, policies and processes, and any regulatory or other requirements
Provide clear guidance on all clinical contracting issues throughout the contracting process
Responsible for overseeing and ensuring a smooth execution and oversight of the entire lifecycle of site contracts
Deep understanding of the end-to-end clinical development paradigm, with expertise in clinical study operations and experience operating in global and/or regional environments
Assist in development and implementation of contract management policies and procedures
Develop, implement, manage and ensure completion of site contracts develop and cultivate excellent internal cross-departmental and external service provider relationships to enable advancement of clinical development programs
Assist in escalations to achieve final scopes of work, budgets, and payment schedules, with input from cross-functional stakeholders, for service providers
Evaluate and monitor contract performance to ensure compliance and mitigate risks
Liaise with legal counsel to address complex contract matters
Extensive experience in site and CRO management, to ensure contracts are executed on a timely basis
Assist in the development, improvement and implementation of processes and tools related to outsourcing and governance activities
With the support of RevMed’s legal counsel, manage the contract negotiation process
Support and manage general and departmental ad hoc projects as required
Participate in corporate strategic initiatives
Monitor shifts in industry trends and technologies
Network with vendors and sites to stay on top of best practices for efficient trial execution by stage of development
Ensure FMV prices are obtained, savings objectives are met and ensure the best interests of RevMed are safeguarded
Promote effective communication and transparency in our CRO/service provider interactions
Initiate, author or otherwise contribute to standard operating procedure (SOP) development, implementation and training
Qualification
Required
BA/BS in Medical or Life Sciences or equivalent, with 10+ years of clinical contracts and budget experience in the pharmaceutical or biotechnology industry
Must have Global Phase 1–3 clinical site agreement and budget negotiation experience
Strong Oncology experience required
Must demonstrate clear understanding of EX US contracting and budgeting process
Must have in-depth knowledge of country-specific contract terms, regulatory requirements, and use, where applicable, of regional clinical site agreement templates
Excellent organizational and time management skills along with strong attention to detail. With proven ability to handle multiple tasks efficiently and effectively
Excellent computer skills including advanced knowledge in MS Excel, Word, PowerPoint and Outlook
Must be a self-starter who works with minimal supervision
Works effectively in a solution cross-functional environment
Excellent communication skills, (verbal and written), and critical thinking skills
High sense of accountability/urgency
Analytical skills with a data driven approach to planning, executing, and problem solving
Extensive experience in global clinical trial operations
Ability to travel to the corporate office quarterly
Preferred
Grant Plan or Grant Manager experience
J.D. a plus
Smartsheet experience
Leadership and management skills
Benefits
Competitive cash compensation
Robust equity awards
Strong benefits
Significant learning and development opportunities
Company
Revolution Medicines
Revolution Medicines is an innovative and dynamic organization of expert biologists, chemists, pharmacologists, clinical scientists.
501-1000 employees
H1B Sponsorship
Revolution Medicines has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (13)
2024 (18)
2023 (15)
2022 (8)
2021 (1)
2020 (2)
Funding
Current Stage
Public CompanyTotal Funding
$2.25BKey Investors
Royalty PharmaBoxer CapitalNextech Invest
2025-06-24Post Ipo Debt· $250M
2024-12-02Post Ipo Equity· $750M
2023-03-02Post Ipo Equity· $323.6M
Leadership Team
Luan Wilfong
Chief Human Resources Officer
Steve Kelsey
President
Recent News
Pharmaceutical Technology
2026-01-13
Company data provided by crunchbase