Syneos Health
Syneos Health
Syneos Health is a fully integrated biopharmaceutical solutions organization that helps clients move therapies from clinical development to commercial delivery. Its teams combine clinical, medical affairs, commercial, technology, and market insights to address changing healthcare needs and support the development and launch of important treatments worldwide.

Lead Clinical Scientist, Gynecologic Oncology (Remote)

Lead clinical science activities for gynecologic oncology programs at Syneos Health, supporting medical data review, safety assessment, and eligibility decisions. Coordinate study teams, project deliverables, expert input, and medical review processes across integrated drug development projects.

Description

  • Partner with the Medical Director to create Medical Management, Medical Data Review, and Eligibility Review Plans
  • Consult external experts, advisors, and consultants to gather medical and scientific guidance
  • Conduct scheduled and as-needed medical reviews of data listings and visualizations
  • Evaluate data for risks, patterns, and trends, and document the resulting medical assessments
  • Draft medical data queries, evaluate responses, and approve query closure with the Medical Director
  • Support patient profile assessments, study-level scientific data reviews, protocol deviation reviews, and Medical Review Summary reports
  • Collaborate with Medical Directors on medical data and safety review meetings, including preparation of presentation materials
  • Oversee project scope, objectives, deliverable quality, milestones, and timelines
  • Act as the main liaison between internal teams, customers, and vendors for medical data and eligibility review activities
  • Work closely with Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management teams
  • Detect and escalate concerns involving data integrity, subject safety, project deliverables, and scope
  • Attend and present at Trusted Process meetings and contribute to internal and external audits
  • Supervise a limited number of direct reports and participate in or lead interviews

Requirements

  • Substantial clinical or medical science experience with deep knowledge of drug development
  • Foundational knowledge of current protocol designs
  • Foundational knowledge of disease terminology and pathology
  • Knowledge of medical data review and eligibility review processes
  • Knowledge of data listings and visualization methods
  • Knowledge of identifying data integrity and subject safety risks
  • Working familiarity with International Council for Harmonisation (ICH) guidelines
  • Working familiarity with Good Clinical Practice (GCP) standards
  • Ability to follow data privacy requirements, enterprise policies, standard operating procedures, work instructions, and project plans
  • Equivalent combinations of experience, skills, or education may be considered

Benefits

  • Opportunities for career development and advancement
  • Supportive, engaged line management
  • Training in technical and therapeutic areas
  • Peer recognition and total rewards program
  • Company car or car allowance
  • Medical, dental, and vision coverage
  • Company 401(k) match
  • Eligibility for the Employee Stock Purchase Plan
  • Eligibility to earn commissions or bonuses based on company and individual performance
  • Flexible paid time off (PTO)
  • Sick time

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