Clinical Scientist, Medical Monitoring – Oncology, Multi-Indication

Syneos Health

. Work with the Medical Director to develop medical plans, including Medical Management, Medical Data Review, and Eligibility Review Plans .

Posted 10/13/2026full-timeRemote • United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Medical Data Review, including the ability to analyze data for risks and trends, author medical data queries, and collaborate effectively with cross-functional teams. Adheres to ICH and GCP guidelines while managing project deliverables and timelines.

Highest-signal resume keywords

Medical Data ReviewData AnalysisMedical Query AuthoringCollaboration with Clinical OperationsAdherence to ICH and GCP

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Medical ManagementData VisualizationEligibility ReviewData ListingsProtocol Deviation ReviewMedical Review SummaryProject ManagementRisk IdentificationData Integrity AssessmentMedical Data Querying

Soft Skills

CollaborationCommunicationProblem-SolvingAttention to DetailAdaptability

Industry Keywords

Good Clinical PracticesInternational Committee on HarmonizationData Privacy GuidelinesClinical OperationsPharmacovigilance

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Work with the Medical Director to develop medical plans, including Medical Management, Medical Data Review, and Eligibility Review Plans
Engage outside experts, consultants, and advisors to obtain medical/scientific input
Perform regular and ad-hoc medical review of data listings and data visualizations
Analyze data to identify risks and patterns/trends and support documentation of medical reviews
Author medical data queries, review responses, and approve query closure with the Medical Director
Assist with patient profile reviews, scientific review of study-level data, protocol deviation review, 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 the primary interface among internal teams, customers, and vendors for medical data and eligibility review
Collaborate with study teams to identify data integrity and subject safety risks
Escalate project concerns, at-risk deliverables, and out-of-scope tasks to project leads
Attend Trusted Process meetings and participate in internal and external audits
Adhere to applicable data privacy, ICH, GCP, company, customer, and project requirements

Requirements

What you’ll need

Knowledge of ongoing protocol designs and disease-related terminology and pathology
Adherence to data privacy guidelines, International Committee on Harmonization (ICH), and Good Clinical Practices (GCPs)
Adherence to enterprise and customer policies, standard operating procedures, work instructions, and project plans
Equivalent experience, skills, and/or education will also be considered
Ability to work with medical data review, eligibility review, data listings, and data visualization
Ability to author medical data queries and review query responses
Ability to collaborate with Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management teams

Benefits

Comp & perks

Career development and progression
Supportive and engaged line management
Technical and therapeutic area training
Peer recognition and total rewards program
Company car or car allowance
Medical, Dental and Vision health benefits
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)
Sick time
Reasonable accommodations when appropriate