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Sitero

DSMB Member – Dermatologist

Sitero

. Review research submissions for regulatory, ethical, and institutional compliance .

Posted 11/5/2026contractRemote • Florida • United StatesMid-LevelSenior💰 $2,000 per dayWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in regulatory compliance, ethical considerations, and clinical research methodologies, particularly in the context of hair disorders and androgenetic alopecia. Possesses strong analytical skills to evaluate safety and efficacy data while maintaining confidentiality and independence in oversight roles.

Highest-signal resume keywords
Advanced Degree In ScienceBoard-Certified PhysicianClinical Experience In Hair Loss ConditionsExperience With Data And Safety Monitoring BoardsRegulatory And Ethical Compliance Expertise

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
Regulatory Compliance ReviewClinical Research EvaluationStatistical Analysis EvaluationRisk AssessmentProtocol Deviation IdentificationSafety MonitoringEfficacy Endpoint FamiliarityData Integrity ReviewClinical InterpretationAdverse Event Assessment
Soft Skills
Confidentiality MaintenanceEffective CommunicationIndependent Review CapabilityCollaborative Participation
Certifications & Qualifications
Board Certification In Medicine
Industry Keywords
Androgenetic AlopeciaHair Restoration StudiesDermatology Clinical ResearchSafety Review CommitteeData And Safety Monitoring BoardResearch EthicsBiostatisticsVeterinary MedicineBiosafetyClinical Trials

About the role

Key responsibilities & impact
  • Review research submissions for regulatory, ethical, and institutional compliance
  • Prepare for and actively participate in scheduled meetings
  • Evaluate risks, benefits, and safeguards within research protocols
  • Identify non-compliance, protocol deviations, or safety concerns
  • Maintain confidentiality of sensitive research information
  • Provide recommendations for approval, modification, suspension, or termination of studies
  • Document reviews and determinations in accordance with institutional policies
  • Remain current with applicable regulations, guidance, and best practices
  • Complete required training and conflict-of-interest disclosures
  • Review interim study data for participant safety and data integrity
  • Assess adverse events, trends, and stopping rules
  • Recommend continuation, modification, or termination of trials
  • Maintain independence from study sponsors and investigators
  • Evaluate statistical analyses and safety monitoring plans
  • Ensure confidentiality of interim data and deliberations
  • Attend scheduled meetings, conduct independent review time before meetings, and participate in ad hoc reviews or urgent matters when needed

Requirements

What you’ll need
  • Advanced degree or equivalent experience in science, medicine, research ethics, regulatory affairs, biostatistics, veterinary medicine, biosafety, or related field (requirements vary by committee)
  • Board-certified physician with expertise in hair disorders and the diagnosis and management of androgenetic alopecia (AGA)
  • Demonstrated clinical and research experience in the evaluation and treatment of hair loss conditions, particularly androgenetic alopecia
  • Previous experience serving as an investigator, sub-investigator, medical monitor, or oversight committee member for androgenetic alopecia clinical trials
  • Familiarity with efficacy and safety endpoints commonly used in hair restoration and hair growth studies, including photographic assessments, hair density measurements, and patient-reported outcomes
  • Experience reviewing safety and efficacy data from dermatology or hair-loss clinical research programs
  • Ability to provide expert clinical interpretation of emerging study data and assess potential risks and benefits for study participants
  • Prior experience serving on a Data and Safety Monitoring Board (DSMB), Safety Review Committee (SRC), or similar independent oversight body preferred
  • Strong understanding of regulatory and ethical considerations related to clinical research involving dermatologic and hair-loss therapies