Clinical/Medical Scientist – Oncology, Hematology

Syneos Health

. Work with the Medical Director to develop medical plans .

Posted 10/2/2026full-timeRemote • New York • United StatesMid-LevelSenior💰 $67,700 - $115,100 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical and medical science, particularly in oncology and hematology, with a strong ability to develop comprehensive medical plans and conduct thorough medical reviews. Proficient in data analysis to identify risks and trends while ensuring adherence to data integrity and safety standards.

Highest-signal resume keywords

Clinical/Medical Science ExperienceMedical Data Review Plan DevelopmentData Analysis for Risk IdentificationMedical Query AuthoringKnowledge of ICH and GCP Guidelines

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Medical Plan DevelopmentData Visualization ReviewData Integrity AnalysisPatient Profile ReviewProtocol Deviation ReviewMedical Review Summary ReportingMedical Data QueryingTrend AnalysisProject ManagementSlide Preparation

Soft Skills

CollaborationCommunicationLeadershipProblem-SolvingInterpersonal Skills

Industry Keywords

OncologyHematologyData Privacy GuidelinesICHGCPSOPsProject PlansClinical OperationsDrug SafetyPharmacovigilance

About the role

Key responsibilities & impact

Work with the Medical Director to develop medical plans
Engage outside experts, consultants, and advisors to obtain medical/scientific input
Perform regular and ad-hoc medical review of data listings and visualizations
Analyze data, identify risks and trends, and document medical reviews
Author medical data queries, review responses, and approve query closure with the Medical Director
Assist with patient profile reviews, study-level scientific data reviews, protocol deviation reviews, and Medical Review Summary reports
Partner with Medical Directors on medical data review and safety review meetings, including slide preparation
Manage project scope, objectives, deliverable quality, milestones, and timelines
Serve as primary interface among internal teams, customers, and vendors for medical data and eligibility review
Collaborate with Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management
Identify and escalate data integrity, subject safety, deliverable, and scope concerns
Attend and present at Trusted Process meetings and participate in internal and external audits
Manage a limited number of direct reports and participate in or conduct interviews

Requirements

What you’ll need

Clinical/medical science experience in oncology and hematology
Ability to develop medical plans, including Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan
Experience performing medical review of data listings and data visualizations
Ability to analyze data to identify risks and data patterns/trends
Ability to author medical data queries and review query responses
Knowledge of patient profile review, study-level scientific data review, and protocol deviation review
Knowledge of ongoing protocol designs and disease-related terminology and pathology
Understanding of data integrity and subject safety risks
Adherence to data privacy guidelines, ICH, GCPs, enterprise policies, SOPs, work instructions, and project plans
Equivalent experience, skills, and/or education will be considered

Benefits

Comp & perks

Career development and progression
Supportive and engaged line management
Technical and therapeutic area training
Peer recognition and total rewards program
Inclusive culture
Company car or car allowance
Medical, dental, and vision health benefits
Company match 401(k)
Employee Stock Purchase Plan eligibility
Eligibility to earn commissions/bonus based on company and individual performance
Flexible paid time off (PTO)
Sick time