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T&M Dentist – Medical Data Reviewer

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ICON
2-5 years
Not Disclosed
Blue Bell, Remote
2 May 7, 2026
Job Description
Job Type: Part Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills:

T&M Dentist – Medical Data Reviewer

Location: Blue Bell, Pennsylvania, United States
Work Mode: Office With Flex
Job Type: Part-Time
Experience Required: Minimum 2–5+ Years in Clinical Research, Medical Data Review, Pharmacovigilance, or Medical Monitoring Preferred
Industry: Clinical Research / Pharmaceutical / CRO / Healthcare


Job Overview

We are seeking a qualified and detail-oriented T&M Dentist – Medical Data Reviewer to support clinical trial data review and medical data validation activities. The selected candidate will play a key role in reviewing clinical and safety data for accuracy, consistency, and protocol compliance while collaborating with clinical operations, pharmacovigilance, and data management teams.

This role is ideal for dental or healthcare professionals with experience in clinical research, medical review, pharmacovigilance, or patient safety within pharmaceutical, biotechnology, or CRO environments.


Key Responsibilities

Clinical Data & Medical Review

  • Perform medical review of:
    • Clinical data listings
    • Patient profiles
    • Safety data
    • Medical records
  • Assess:
    • Medical plausibility
    • Data consistency
    • Protocol adherence
    • Clinical accuracy
  • Ensure high-quality and reliable clinical trial data for study outcomes.

Safety Data Analysis & Query Resolution

  • Identify:
    • Potential safety signals
    • Data discrepancies
    • Clinical inconsistencies
    • Adverse event trends
  • Collaborate with study teams to resolve:
    • Medical queries
    • Data clarification requests
    • Coding issues
    • Reconciliation activities
  • Support safety database review processes where applicable.

Clinical Trial Support & Regulatory Compliance

  • Support preparation for:
    • Database locks
    • Interim analyses
    • Regulatory submissions
    • Clinical milestones
  • Ensure compliance with:
    • ICH-GCP guidelines
    • Clinical trial protocols
    • Regulatory standards
    • Sponsor SOPs

Medical Review Planning & Process Improvement

  • Contribute to development and improvement of:
    • Medical review plans
    • Review guidelines
    • Data review tools
    • Quality review workflows
  • Participate in continuous improvement initiatives to enhance review efficiency and data quality.

Cross-Functional Collaboration

  • Collaborate with:
    • Clinical Operations teams
    • Pharmacovigilance teams
    • Data Management teams
    • Medical reviewers
    • Regulatory stakeholders
  • Ensure smooth communication and coordination across global study teams.

Required Qualifications

Educational Qualifications

Required Qualification:

  • Medical or healthcare qualification such as:
    • DDS / DMD (Dentist)
    • MD
    • MBBS
    • PharmD
    • Or equivalent healthcare qualification

Alternative Qualification

  • Life Sciences degree with strong clinical or medical review experience may also be considered.

Experience Requirements

Required Experience

  • Experience in:
    • Clinical Research
    • Pharmacovigilance
    • Medical Monitoring
    • Medical Data Review
    • Clinical Safety Operations
  • Strong understanding of:
    • Clinical trial design
    • Safety reporting
    • Medical terminology
    • GCP guidelines

Preferred Experience

  • Minimum 2–5+ years of relevant experience in:
    • CRO environments
    • Pharmaceutical industry
    • Clinical trial operations
    • Medical data review activities

Freshers Eligibility

  • Freshers are generally not preferred for this role.
  • Candidates with strong clinical backgrounds and some exposure to:
    • Clinical research
    • Medical review
    • Pharmacovigilance
      may still be considered.

Required Technical Skills

Clinical & Medical Review Skills

  • Medical Data Review
  • Clinical Trial Data Analysis
  • Patient Safety Review
  • Adverse Event Analysis
  • Medical Monitoring
  • Protocol Compliance
  • Clinical Documentation Review

Regulatory & Compliance Skills

  • ICH-GCP Guidelines
  • Safety Reporting
  • Regulatory Compliance
  • Clinical Trial Standards
  • Data Reconciliation
  • Audit Readiness