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Senior Director, Clinical Business Operations

Olema Oncology
Full-time
Remote friendly (Boston, MA)
United States
$225,000 - $265,000 USD yearly
Clinical Research and Development

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Role Summary

Senior Director, Clinical Business Operations. Based in San Francisco or Cambridge, with approximately 10-15% travel. Leads the clinical outsourcing strategy and vendor management to support clinical trials, reporting to the SVP of Clinical Operations.

Responsibilities

  • Oversee communication with clinical vendors regarding contracts, scope of work, and budgets
  • Lead the Request for Proposal (RFP) and vendor bidding process for clinical trials, including writing of RFP, bid comparison analysis, manage bid defense meetings, and vendor scorecard development
  • Manage the identification of service providers for clinical studies in collaboration with the study management teams and clinical departments
  • Liaise with the legal and financial groups on the vendor contract and purchase order process for the Clinical Department and negotiate terms of contract as needed
  • Work with clinical department partners to build the Scope of Work (SOW) for the contract including negotiation of costs
  • Review all change notification forms (CNFs) and Change Orders (COs) with contract manager and finance to ensure that correct pricing is established
  • Liaise with the legal and financial groups on the vendor contract and purchase order process for the Clinical Department
  • Establish strong partnerships with the clinical vendors to understand contracting challenges and develop simplified and collaborative resolutions to these challenges
  • Drive the Fair Market Value (FMV) process through working with the study teams and vendors to analyze and negotiate the final work order and subsequent change orders
  • Establish and manage the vendor governance process with key clinical vendors. Document key decisions and action plans and ensure compliance with the decisions established in governance meetings
  • Work with study teams to establish KPI process and help establish standard clinical vendor KPIs to enhance vendor oversight and performance
  • Collaborate with legal and clinical operations teams to establish template clinical site contracts/clinical trial agreements (CTAs)
  • Interact with finance and clinical operations teams to build template site budget utilizing a FMV tool. In some studies, may help negotiate these budgets with clinical sites
  • Attend Study Execution Team (SET), monthly budget, and clinical meetings; may present as needed
  • Provide insight and feedback at Clinical Operations Leadership Team
  • Lead in clinical outsourcing process/tool development, improvement, and implementation

Qualifications

  • 15+ years of experience working in clinical research, biotech, and/or pharmaceutical company
  • Experience managing clinical outsourcing or procurement professionals
  • Expertise in building RFPs and leading the vendor selection process
  • Strong experience in vendor and site CTA contracting/budgeting, FMV assessment, Scientific Collaborator engagement to conduct clinical trials
  • Experience in providing thought leadership and consistent customer service
  • Expertise in the clinical contracting process, including CDAs, SOW, FMV assessment, contract negotiations and management, Work Orders, Change Orders, and Budget process
  • Demonstrated leadership skills in fast-paced and changing environments
  • BS or MS in a relevant discipline is required

Skills

  • Writing, critical analysis/evaluation, benchmarking, contracting, and negotiating
  • Strategic and integrative thinking to establish outsourcing norms across the Clinical Department
  • Knowledge of clinical development programs and regulatory environments
  • Cost estimation and FMV tooling proficiency
  • Strong interpersonal, negotiation, and relationship-building abilities

Education

  • BS or MS in a relevant discipline

Additional Requirements

  • Role based in San Francisco or Cambridge; some travel required (~10-15%)
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