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Precision Medicine Group

Senior Director, Scientific Affairs

Precision Medicine Group

. Drive and support operational considerations for RFPs and bid defense meetings .

Posted 10/6/2026full-timeRemote • United StatesSenior💰 $181,400 - $225,000 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in managing global laboratory operations, including oversight of third-party lab relationships and operational protocol analysis. Proven ability to lead teams, develop strategic proposals, and ensure compliance with clinical development standards.

Highest-signal resume keywords
Global Laboratory Network ManagementOperational Protocol AnalysisClinical Development StrategyThird-Party Lab OversightBudget Development

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Operational Specifications DevelopmentProposal Text DevelopmentMetrics ReportingFeasibility AnalysisQuality Systems EstablishmentClinical Trial ExecutionEnrollment PlanningStudy Timeline ManagementAssay Specification InterpretationBudget Review
Soft Skills
Team LeadershipMentoringCollaborationCommunicationInfluencing
Certifications & Qualifications
Bachelor's Degree in Life SciencesPhD Preferred
Industry Keywords
CRO IndustryLab OperationsClinical TrialsOperational DeliveryCompliance ObjectivesStrategic PlanningBid Defense MeetingsInnovation SupportScientific Landscape InputPost-Award Meetings

About the role

Key responsibilities & impact
  • Drive and support operational considerations for RFPs and bid defense meetings
  • Own global third-party lab relationships
  • Represent Precision lab operations at pre-award, internal and external kick-off meetings
  • Lead projects supporting innovation and competitive advantage
  • Collaborate with scientific, operational, business development, proposal, and functional leadership teams
  • Hire, train, develop, and mentor direct reports
  • Own, maintain, and report staff and department metrics
  • Develop operational specifications from client protocols, including enrollment, feasibility, study timelines, and startup timelines
  • Interpret protocols and assay specifications for global laboratories
  • Attend post-award monthly and governance meetings; collect metrics and reconcile invoices and billing
  • Create specification sheets and obtain quote information
  • Develop and review proposal text, including third-party lab quotes
  • Ensure proposals reflect strategic, operational, scientific, and clinical development planning
  • Support study proposal budgets for internal laboratories and third-party lab partners
  • Transition operational strategy to lab operations ahead of internal kick-off meetings
  • Participate in post-award meetings to support study execution
  • Mentor and train scientific affairs and Precision colleagues
  • Support capabilities presentations and pre-award client meetings
  • Provide feasibility and scientific landscape input for bid defense meetings
  • Collaborate on innovative client solutions
  • Support post-award delivery of data and milestones
  • Represent the company at industry meetings, speaking engagements, and booth exhibitions
  • Publish scientific or industry-related articles

Requirements

What you’ll need
  • Bachelor's degree in life sciences discipline or equivalent relevant experience
  • Advanced degree PhD preferred
  • 15+ years in the CRO/Lab industry or equivalent relevant experience and/or demonstrated competencies
  • Experience leading and influencing a global laboratory network, including oversight of multi-site laboratory operations
  • Experience establishing standardized processes and quality systems
  • Experience aligning regional laboratories to enterprise-wide strategic, operational, and compliance objectives
  • Experience in operational protocol analysis and budget review
  • Strong experience in Precision’s identified target therapeutic area clinical development focused on operational delivery considerations, strategy, feasibility, budget development and operational execution of all phases of clinical trials
  • Management or oversight of third party lab partners
  • Candidates must be legally authorized to work in the country of employment without employer sponsorship

Benefits

Comp & perks
  • Discretionary annual bonus
  • Health insurance
  • Retirement savings benefits
  • Life insurance
  • Disability benefits
  • Parental leave
  • Paid time off for sick leave and vacation