Medical Scientist, ONC – Bladder Late Phase

Syneos Health

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

Posted 10/9/2026full-timeRemote • United StatesMid-LevelSenior💰 $67,700 - $139,600 per yearWebsite

Core Competencies

Role fit

Core Competencies

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

Demonstrates expertise in Medical Data Review, Eligibility Review, and adherence to ICH and GCP guidelines. Capable of analyzing data for risks and trends while collaborating effectively with cross-functional teams.

Highest-signal resume keywords

Medical Data ReviewEligibility ReviewData AnalysisProject ManagementCollaboration with Clinical Operations

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 VisualizationProtocol Deviation ReviewMedical Review Summary ReportsData Integrity Assessment

Soft Skills

CollaborationCommunicationProblem-Solving

Industry Keywords

ICH GuidelinesGCPsData Privacy GuidelinesStandard Operating ProceduresProject Plans

About the role

Key responsibilities & impact

Work with the Medical Director to develop Medical Management, Medical Data Review, and Eligibility Review Plans
Engage outside experts, consultants, and advisors to obtain medical/scientific input for medical plans
Perform regular and ad-hoc medical review of data listings and data visualizations
Analyze data to identify risks and patterns/trends and document medical reviews
Identify and resolve medical data review issues
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 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 study teams to identify data integrity and subject safety risks
Escalate study concerns, at-risk deliverables, and out-of-scope tasks to project leads
Participate in internal and external audits
Participate in or conduct interviews

Requirements

What you’ll need

Equivalent experience, skills, and/or education will also be considered
Basic understanding and knowledge of ongoing protocol designs and disease-related terminology and pathology
Adherence to data privacy guidelines, ICH, GCPs, enterprise policies, standard operating procedures, work instructions, and project plans
Adherence to customer policies and standard operating procedures, as required in project plans
Ability to work with medical data review, eligibility review, data listings, and data visualization
Ability to collaborate with Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management
Ability to participate in or conduct interviews
Ability to participate in internal and external audits

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)
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