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Syneos Health

Clinical Scientist, Medical Monitoring – Oncology – Breast

Syneos Health

Clinical/Medical Scientist developing medical plans and ensuring quality deliverables in drug development processes. Collaborating with Medical Directors and study teams to maintain project timelines and data integrity.

Posted 7/18/2026full-timeRemote • North Carolina • 🇺🇸 United StatesMid-LevelSenior💰 $67,700 - $115,100 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in developing medical plans, conducting medical data reviews, and managing project deliverables while ensuring compliance with data privacy guidelines and Good Clinical Practices. Collaborates effectively with cross-functional teams to uphold data integrity and subject safety.

Highest-signal resume keywords
Medical Management Plan DevelopmentMedical Data ReviewProject Scope ManagementData VisualizationGood Clinical Practices (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 Listings ReviewEligibility Review PlanAd-Hoc Medical ReviewScientific Review
Soft Skills
CollaborationCommunication
Industry Keywords
International Committee on Harmonization (ICH)Data IntegritySubject SafetyClinical OperationsPharmacovigilance

About the role

Key responsibilities & impact
  • Works with Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan)
  • Performs regular and ad-hoc medical review of data listings and data visualization as needed
  • Authors medical data queries and reviews query responses
  • Partners with Medical Directors for medical data review meetings and safety review meetings
  • Manages project scope of work, objectives, and quality of deliverables to ensure the project specific milestones and timelines are met
  • Collaborates with study team members including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management
  • Attends and present at Trusted Process meetings

Requirements

What you’ll need
  • Works with Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan)
  • Performs regular and ad-hoc medical review of data listings and data visualization as needed
  • authors medical data queries and reviews query responses
  • may assist Medical Director in patient profiles review, scientific review of other study level data
  • manages project scope of work, objectives, and quality of deliverables
  • collaborates with study team members to identify risks related to data integrity and subject safety
  • adheres to all data privacy guidelines, International Committee on Harmonization (ICH), and Good Clinical Practices (GCPs)

Benefits

Comp & perks
  • company car or car allowance
  • 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