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Syneos Health

Senior Clinical Scientist – Medical Monitoring, Oncology – Breast

Syneos Health

Sr Clinical/Medical Scientist in Oncology at Syneos Health developing medical plans and conducting data reviews. Collaborate with cross-functional teams to ensure project deliverables.

Posted 7/18/2026full-timeRemote • Maryland • 🇺🇸 United StatesSenior💰 $79,800 - $139,600 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in developing medical plans and conducting thorough medical reviews, while ensuring compliance with data privacy guidelines and Good Clinical Practices. Capable of collaborating effectively with cross-functional teams and managing project deliverables.

Highest-signal resume keywords
Medical Plan DevelopmentMedical Data ReviewData AnalysisCollaboration with Cross-Functional TeamsCompliance with ICH and GCP

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
Medical Data QueriesData VisualizationRisk IdentificationData Pattern AnalysisProject Scope Management
Soft Skills
CollaborationCommunicationPresentation SkillsLeadership
Industry Keywords
Data Privacy GuidelinesGood Clinical PracticesInternational Committee on HarmonizationClinical OperationsPharmacovigilance

About the role

Key responsibilities & impact
  • Develop medical plans in collaboration with Medical Director
  • Conduct medical reviews of data listings and visualization
  • Author and manage medical data queries
  • Collaborate with project teams on medical data review
  • Attend and present at meetings, including internal and external audits
  • Comply with data privacy guidelines and standard operating procedures
  • May manage limited number of direct reports

Requirements

What you’ll need
  • Works with Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan)
  • Engages with outside experts/consultants/advisors to coordinate the acquisition of necessary medical/scientific input to prepare respective medical plans
  • Performs regular and ad-hoc medical review of data listings and data visualization as needed
  • Analyzes the data to identify risks and data patterns/trends
  • Authors medical data queries and reviews query responses
  • May assist Medical Director in patient profiles review
  • Manages project scope of work, objectives, and quality of deliverables
  • Collaborates with study team members including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management
  • Adheres to all data privacy guidelines, International Committee on Harmonization (ICH), and Good Clinical Practices (GCPs)

Benefits

Comp & perks
  • Health benefits to include Medical, Dental and Vision
  • Company match 401k
  • Eligibility to participate in Employee Stock Purchase Plan
  • Eligibility to earn commissions/bonus based on company and individual performance
  • Flexible paid time off (PTO) and sick time