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Lifelancer

Medical Director/Senior Medical Director – Endocrinology

Lifelancer

. Provide medical oversight of clinical trials to ensure SOPs, client directives, good clinical practice, and regulatory requirements are followed .

Posted 9/24/2026full-timeRemote • North Carolina • United States, CanadaSenior💰 $200,000 - $278,900 per yearWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in medical oversight of clinical trials, ensuring compliance with SOPs, regulatory requirements, and good clinical practice. Proficient in medical review, analysis of adverse events, and providing consultation to stakeholders in clinical settings.

Highest-signal resume keywords
MD Or EquivalentFormal Training In Endocrinology Diabetes & MetabolismClinical Trial ExperienceTherapeutic Expertise In NeurologyUnderstanding Of FDA, ICH, EMA, And GCP Guidelines

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Medical ReviewData Review And ValidationSignal DetectionAdverse Event MonitoringBiostatisticsClinical Operations ProceduresPatient Treatment ExperienceCoding ListingsTherapeutic And Protocol TrainingMedical Consultation
Soft Skills
Excellent Oral And Written CommunicationInterpersonal SkillsInfluencing SkillsTeam-Building SkillsAbility To Mentor And Train
Tools & Technologies
Safety DatabasesMedDRABasic Computer Applications
Certifications & Qualifications
Active Medical Licensure Preferred
Industry Keywords
Clinical TrialsGood Clinical PracticeRegulatory RequirementsPharmacovigilanceRisk Management Activities

About the role

Key responsibilities & impact
  • Provide medical oversight of clinical trials to ensure SOPs, client directives, good clinical practice, and regulatory requirements are followed
  • Manage and oversee contracted services
  • Attend and present at investigator and sponsor meetings
  • Provide medical consultation to clients, investigators, project team members, and internal team members
  • Support business development activities
  • Provide medical review and analysis of clinical trial serious adverse events
  • Ensure tasks delegated to medical monitors are properly executed
  • Monitor adverse events, laboratory abnormalities, patient medical status, concomitant medications, and un-blinding requests
  • Discuss medical concerns with principal investigators and clients and apply medical judgment to clinical situations
  • Medically review adverse events of special interest, serious adverse events, and clinical outcome events
  • Perform data review and validation, including coding listings and safety data, to identify potential safety concerns
  • Provide therapeutic and protocol training
  • Write or review CSRs, IND/NDA reports, ICSRs, signal detection reports, periodic reports, RMPs, REMS, and CTD modules
  • Manage signal detection activities and scientifically review aggregate reports
  • Contribute to label updates, dossier maintenance, and risk management activities
  • Medically review adverse-event and serious-adverse-event data from solicited, spontaneous, and literature sources

Requirements

What you’ll need
  • MD or equivalent required
  • Formal training in Endocrinology Diabetes & Metabolism (residency and/or fellowship)
  • Patient treatment experience comparable to 2 years
  • For Senior Medical Director: suitable clinical trial experience in a CRO, pharmaceutical company, or as a principal investigator comparable to 1–2 years, or direct safety/Pharmacovigilance experience comparable to 2 years
  • Active medical licensure preferred but not required
  • Must be legally authorized to work in the United States or Canada without sponsorship
  • Must be able to pass a comprehensive background check, including drug screening where applicable
  • Therapeutic expertise in Neurology
  • Working knowledge of relevant safety databases, e.g. MedDRA
  • Understanding of FDA, ICH, EMA, and GCP guidelines
  • Working knowledge of biostatistics, data management, and clinical operations procedures
  • Proficiency in basic computer applications
  • Fluent in spoken and written English
  • Ability to travel domestically and internationally
  • Ability to work independently, analyze and prioritize sensitive complex information, and multitask
  • Excellent oral and written communication, interpersonal, influencing, and team-building skills
  • Ability to mentor and train other staff

Benefits

Comp & perks
  • Annual incentive plan bonus
  • Healthcare
  • Range of employee benefits
  • Career and development prospects
  • Innovative, forward-thinking company culture