Clinical Scientist – Oncology

Syneos Health

Clinical Scientist developing medical plans and performing data analysis for biopharmaceutical solutions. Collaborating with Medical Directors and cross-functional teams in a remote role.

Posted 7/29/2026full-timeRemote • Arizona, Maine, North Carolina, Ohio, Rhode Island • 🇺🇸 United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in developing medical plans, conducting medical data reviews, and ensuring compliance with Good Clinical Practices (GCPs) and International Committee on Harmonization (ICH) guidelines. Proficient in collaborating with cross-functional teams to manage project deliverables and maintain data integrity.

Highest-signal resume keywords

Medical Data ReviewProject ManagementGood Clinical Practices (GCPs)International Committee on Harmonization (ICH)Data Analysis

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Medical Management Plan DevelopmentMedical Data Review Plan DevelopmentEligibility Review Plan DevelopmentData VisualizationMedical Data Query AuthoringProtocol Deviation ReviewMedical Review Summary Report CreationRisk IdentificationData Integrity AnalysisScientific Review

Soft Skills

CollaborationCommunicationInterpersonal SkillsOrganizational Skills

Industry Keywords

Clinical OperationsData ManagementDrug SafetyPharmacovigilanceTrusted ProcessData Privacy Guidelines

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)
Engages with outside experts/consultants/advisors to coordinate the acquisition of necessary medical/scientific input to prepare the 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 and supports documentation of medical reviews
Authors medical data queries and reviews query responses, approves query closure in association with Medical Director
May assist Medical Director in patient profiles review, scientific review of other study level data, protocol deviation review, creation of Medical Review Summary report as needed
Partners with Medical Directors for medical data review meetings and safety review meetings including slide preparation as needed
Manages project scope of work, objectives, and quality of deliverables to ensure the project specific milestones and timelines are met
Serves as primary interface between internal team, customers, and vendors in the areas of medical data review and eligibility review
Collaborates with study team members including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management (set-up and/or lead meetings as appropriate) to identify risks related to data integrity and subject safety
Attends at Trusted Process meetings and may participate in internal and external audits
Acquires basic understanding and knowledge of ongoing protocol designs and disease related terminology and pathology
Adheres to all data privacy guidelines, International Committee on Harmonization (ICH), and Good Clinical Practices (GCPs), all enterprise policies, standard operating procedures, work instructions, and project plans
Adheres to customer policies and standard operating procedures, as required in project plans

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 the 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 and supports documentation of medical reviews
Authors medical data queries and reviews query responses, approves query closure in association with Medical Director
May assist Medical Director in patient profiles review, scientific review of other study level data, protocol deviation review, creation of Medical Review Summary report as needed
Partners with Medical Directors for medical data review meetings and safety review meetings including slide preparation as needed
Manages project scope of work, objectives, and quality of deliverables to ensure the project specific milestones and timelines are met
Serves as primary interface between internal team, customers, and vendors in the areas of medical data review and eligibility review
Collaborates with study team members including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management (set-up and/or lead meetings as appropriate) to identify risks related to data integrity and subject safety
Attends at Trusted Process meetings and may participate in internal and external audits
Acquires basic understanding and knowledge of ongoing protocol designs and disease related terminology and pathology
Adheres to all data privacy guidelines, International Committee on Harmonization (ICH), and Good Clinical Practices (GCPs), all enterprise policies, standard operating procedures, work instructions, and project plans
Adheres to customer policies and standard operating procedures, as required in project plans

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