Senior Medical Director – Immunology/Rheumatology

Syneos Health

Medical Director overseeing immunology/rheumatology clinical studies with a focus on drug safety and pharmacovigilance. Collaborating with project teams and providing training on protocols and guidelines.

Posted 7/14/2026full-timeRemote • North Carolina • 🇺🇸 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 leading medical responses to RFPs and providing therapeutic training to project teams.

Highest-signal resume keywords

Medical OversightProtocol DesignDrug SafetyGood Clinical Practice (GCP)Therapeutic Training

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study OversightData Collection ToolsMonitoring PlansReview and Analysis PlansFeasibility AssessmentSubject IdentificationMedical InputRegulatory KnowledgeProtocol DevelopmentMedical Responses to RFPs

Soft Skills

LeadershipCollaborationCommunication

Industry Keywords

Drug Development RegulationsPharmacovigilanceBid Defense MeetingsClinical Data ReviewICH Guidelines

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
Provides medical input and oversight in support of the Drug Safety and Pharmacovigilance department
Develops and delivers project-specific and therapeutic training to project team members and clinical site staff
Provides medical input into data collection tools, monitoring plans, and review and analysis plans
Provides oversight to assigned Medical Scientist staff and Medical Director colleagues to review clinical data

Requirements

What you’ll need

Provides medical oversight of assigned clinical studies in the duty as a medical monitor
Responsible for protocol design and development, upon request
Provides medical and therapeutic input to Study Start Up, Feasibility, and Subject Identification efforts
Maintains in-depth knowledge of FDA and worldwide drug development regulations and national and ICH Good Clinical Practice (GCP) guidelines
Leads medical responses to Requests for Proposals (RFPs) and Bid Defense Meetings (BDMs)

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