Clinical Medical Scientist – Medical Monitoring, Infectious Disease

Syneos Health

. Develop medical plans with the Medical Director, including Medical Management, Medical Data Review, and Eligibility Review Plans .

Posted 9/15/2026full-timeRemote • United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in medical data analysis, medical monitoring in HIV clinical trials, and adherence to ICH/GCP guidelines. Proficient in managing project deliverables and collaborating effectively with cross-functional teams.

Highest-signal resume keywords

Medical Monitoring ExperienceHIV Clinical TrialsICH/GCP Guidelines ProficiencyMedical Data AnalysisProject Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Medical Data ReviewData AnalysisMedical Query AuthoringProtocol Deviation ReviewEligibility ReviewScientific ReviewData VisualizationRisk IdentificationMedical Review Summary ReportingUnderstanding of Disease Terminology

Soft Skills

Excellent Time ManagementStrong Interpersonal SkillsEffective CommunicationSelf-StarterTroubleshooting Ability

Tools & Technologies

MS OfficeSpreadsheetsPresentations

Industry Keywords

Life Sciences DegreeClinical TrialsDrug DevelopmentData Privacy GuidelinesSOPs

About the role

Key responsibilities & impact

Develop medical plans with the Medical Director, including Medical Management, Medical Data Review, and Eligibility Review Plans
Coordinate acquisition of medical/scientific input from outside experts, consultants, and advisors
Perform regular and ad-hoc medical review of data listings and 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 Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management teams to identify data integrity and subject safety risks
Escalate study concerns, at-risk deliverables, and out-of-scope tasks to project leads
Attend and present at Trusted Process meetings and participate in internal and external audits
Maintain understanding of protocol designs, disease terminology, and pathology
Follow data privacy guidelines, ICH, GCPs, company policies, SOPs, work instructions, and project plans

Requirements

What you’ll need

Degree in life sciences (BS, MSc, PharmD, PhD)
Medical monitoring experience in HIV clinical trials required
Excellent time management skills to handle multiple tasks and meet deadlines in a highly regulated and dynamic environment
Self-starter comfortable with fluctuating timelines, work demands, and changes in scope of work
Ability to troubleshoot situations and escalate issues or questions when needed
Understanding of scientific principles for effective, high-quality medical data analysis
Excellent written and oral communication skills
Excellent computer skills, including MS Office programs, spreadsheets, and presentations
Knowledge of drug development and demonstrated proficiency with ICH/GCP guidelines
Strong interpersonal skills and ability to work effectively in a cross-functional team environment
May travel up to 25%

Benefits

Comp & perks

Career development and progression
Supportive and engaged line management
Technical and therapeutic area training
Peer recognition and total rewards program
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) and sick time
Company car or car allowance may be included