Senior Director – Medical Monitor, Immunology/Rheumatology

Syneos Health

Medical Monitor overseeing clinical studies and providing medical oversight in drug development. Collaborate with teams and customers to ensure the integrity of projects and subject safety.

Posted 7/2/2026full-timeRemote • Florida, Illinois, North Carolina, Texas, Washington • 🇺🇸 United StatesSenior💰 $146,000 - $332,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in medical oversight of clinical studies, including protocol design and development, while ensuring compliance with FDA regulations and ICH Good Clinical Practice guidelines. Capable of providing training and mentorship to project teams and clinical site staff, with a focus on drug safety and pharmacovigilance.

Highest-signal resume keywords

Medical OversightProtocol DesignDrug SafetyPharmacovigilanceGood Clinical Practice (GCP)

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study OversightProtocol DevelopmentData ReviewTrend AnalysisRisk Mitigation

Soft Skills

MentoringTraining DeliveryCommunication

Industry Keywords

FDA RegulationsICH GuidelinesTherapeutic Area ExpertiseClinical Data IntegrityScientific Meetings

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Provides medical oversight of assigned clinical studies in the duty as a medical monitor
Often serves as primary medical contact for customers for assigned clinical studies
Provides medical input and oversight in support of the Drug Safety and Pharmacovigilance department
Responsible for protocol design and development, upon request
Provides input into protocol amendments
Develops and delivers project-specific and therapeutic training to project team members and clinical site staff; provides training to customer staff as needed
Provides oversight to assigned Medical Scientist staff and Medical Director colleagues to review clinical data
Presents identified trends and issues, and mitigation strategies, to customers and project team members to minimize risks to subject safety or integrity of study data
Represents the Company at scientific and industry meetings
Mentors staff to ensure an appropriate level of understanding regarding sound treatment and research principles of specific therapeutic area

Requirements

What you’ll need

Provides medical oversight of assigned clinical studies in the duty as a medical monitor
Often serves as primary medical contact for customers for assigned clinical studies
Provides medical input and oversight in support of the Drug Safety and Pharmacovigilance department
Responsible for protocol design and development, upon request
Provides input into protocol amendments
Develops and delivers project-specific and therapeutic training to project team members and clinical site staff; provides training to customer staff as needed
Provides medical and therapeutic input to Study Start Up, Feasibility, and Subject Identification efforts
Provides oversight to assigned Medical Scientist staff and Medical Director colleagues to review clinical data
Maintains in-depth knowledge of FDA and worldwide drug development regulations and national and ICH Good Clinical Practice (GCP) guidelines
Represents the Company at scientific and industry meetings

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