Medical Director, Medical Affairs – Neurology

Worldwide Clinical Trials

. Provide medical oversight and serve as the assigned Medical Monitor for clinical research studies.

Posted 10/7/2026full-timeRemote • United StatesLead💰 $134,500 - $267,500 per yearWebsite

Core Competencies

Role fit

Core Competencies

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

Demonstrates expertise in medical monitoring and clinical research, with a strong foundation in GCP, safety processes, and regulatory compliance. Capable of leading global trials, mentoring colleagues, and effectively communicating with cross-functional teams.

Highest-signal resume keywords

Medical Monitoring ExperienceKnowledge of GCPClinical Development ExpertiseSafety Data ReviewExcellent Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Medical DegreeClinical ResearchSerious Adverse Event ManagementProtocol DevelopmentClinical Study Report Review

Soft Skills

Organizational SkillsTime ManagementPresentation Skills

Tools & Technologies

Microsoft WordMicrosoft ExcelMicrosoft Access

Industry Keywords

Clinical TrialsRegulatory ComplianceMedical OversightCross-Functional CollaborationSponsor Engagement

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Provide medical oversight and serve as the assigned Medical Monitor for clinical research studies.
Lead global and pan-regional trials as a Global Lead Medical Monitor.
Review and support the medical management of serious adverse events with Medical & Safety teams.
Deliver protocol-specific and therapeutic area training to project teams.
Contribute clinical and scientific expertise to study protocols, clinical development programs, research publications, and medical deliverables.
Support sponsor engagement and business development activities, including feasibility assessments, proposal development, and client meetings.
Review and contribute to clinical study reports and key study documentation.
Partner with cross-functional teams to ensure project delivery, regulatory compliance, and client satisfaction.
Mentor and support medical colleagues.

Requirements

What you’ll need

Medical Degree from an accredited institution of medical education.
At least 2 years of medical monitoring experience within clinical research or a related industry.
Strong knowledge of GCP, clinical development, safety processes, and applicable regulatory requirements.
Experience reviewing safety data and supporting serious adverse event assessment and management.
Excellent written and verbal communication, presentation, organizational, and time management skills.
Strong computer proficiency, including Microsoft Word, Excel, and Access.
Proficiency in English.
Valid passport and ability to travel as required.

Benefits

Comp & perks

Competitive benefits package depending on location
Inclusive and equitable workplace
Transparent compensation and pay equity