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Clinical Research Physician (Md/Do)

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ICON
1-3 years
Not Disclosed
Kansas City, Lenexa, Remote
2 May 7, 2026
Job Description
Job Type: Full Time Education: MD/DO degree Skills: Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Research Physician (MD/DO)

Location: Lenexa, Kansas, United States
Work Mode: Onsite
Job Type: Full-Time
Working Hours: Monday – Friday | 7:00 AM – 3:00 PM
Experience Required: MD/DO with Clinical Experience; Clinical Research Experience Preferred
Industry: Clinical Research / Healthcare / Pharmaceutical / CRO


Job Overview

We are seeking a highly skilled and patient-focused Clinical Research Physician (MD/DO) to join a leading clinical research team in Lenexa, Kansas. The selected candidate will play a critical role in conducting clinical evaluations, overseeing subject safety, monitoring adverse events, supporting protocol implementation, and ensuring regulatory compliance for early-phase clinical research studies.

This role is ideal for licensed physicians interested in clinical trials, patient safety, protocol management, and translational medical research within a pharmaceutical or CRO environment.


Key Responsibilities

Clinical Evaluations & Patient Safety

  • Conduct comprehensive:
    • Medical history reviews
    • Physical examinations
    • Clinical assessments
    • Safety evaluations
      for healthy volunteers and patients participating in clinical research studies.
  • Review:
    • Laboratory reports
    • Eligibility criteria
    • Safety parameters
    • Medical findings
      in accordance with study protocols.
  • Ensure participant safety throughout all study phases.

Clinical Trial Oversight & Protocol Compliance

  • Supervise study conduct and ensure strict adherence to:
    • Clinical protocols
    • ICH-GCP guidelines
    • Regulatory requirements
    • Sponsor standards
  • Prescribe study medications and ensure proper dosage and administration procedures.
  • Participate in:
    • Protocol development
    • Ethics committee discussions
    • Clinical reporting activities
    • Study review meetings

Adverse Event Monitoring & Medical Decision Making

  • Monitor subjects for:
    • Adverse events (AEs)
    • Safety concerns
    • Clinical abnormalities
  • Perform medical review and clinical assessment of adverse events.
  • Initiate appropriate medical interventions and safety actions when required.
  • Present safety findings during clinical and project meetings.

Clinical Operations & Study Documentation

  • Complete and maintain:
    • Case Report Forms (CRFs)
    • Clinical documentation
    • Study records
    • Safety reports
  • Assist with:
    • Venous access procedures
    • Sample collection
    • Safety monitoring activities
  • Ensure documentation accuracy, compliance, and audit readiness.

Cross-Functional Collaboration

  • Collaborate with:
    • Nursing teams
    • Clinical Operations
    • Sponsors
    • Investigators
    • Regulatory stakeholders
  • Maintain effective communication across interdisciplinary teams to support successful study execution.

Industry Knowledge & Professional Development

  • Stay updated on:
    • Clinical research regulations
    • Medical advancements
    • Pharmaceutical industry trends
    • Best practices in patient safety
  • Contribute to training and continuous professional development initiatives.

Required Qualifications

Educational Qualifications

Required Qualification:

  • Medical Degree:
    • MD
    • DO
    • Or equivalent medical qualification

Preferred Specializations

  • Internal Medicine
  • Family Medicine
  • Other medical specialties may also be considered

Licensure Requirements

  • Active medical licensure required
  • Current Kansas State Medical License preferred
  • Or ability to obtain Kansas State Medical Licensure