Clinical Research Investigator (MD/DO)

DM Clinical Research

Baltimore, MDFull-timePosted Apr 1, 2026

Behavioral Health Market Context

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Job Description

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• Ensures the medical well-being and safety of the participants through the safe performance and execution of the studies.
• Assists in maintaining clinical oversight and quality on the studies registered on and delivers on study targets, thereby contributing to the commercial success of the site.
• Reviews enrollment progress, pre-screening and screening success rates, screen failure rates, safety, and retention of participants.
• Interprets protocols and IB and participates in initiatives to strategize for patient recruitment.
• Carries out clinical evaluation and assessment of participants to ensure eligibility to enroll in studies.
• Ensures and protects the welfare and safety of participants through ethical conduct.
• Fulfills and complies with all medical duties as per protocol, SOP/COP and ICH GCP and local regulations.
• Exercises meticulous attention to detail in documentation and patient care.
Requirements
• Medical license (MD, DO) - Maryland
• 2 years experience as a Clinical Research Investigator (Principal Investigator or Sub-Investigator)
• Bilingual Spanish a plus

Flexible hours - schedule can be tailored as required.

Qualifications

  • Medical license (MD, DO) - Maryland
  • 2 years experience as a Clinical Research Investigator (Principal Investigator or Sub-Investigator)
  • Flexible hours - schedule can be tailored as required

Benefits

    Responsibilities

    • This individual will conduct all clinical trials (studies) according to ICH, GCP, local regulations, study protocols, and company processes
    • Ensures the medical well-being and safety of the participants through the safe performance and execution of the studies
    • Assists in maintaining clinical oversight and quality on the studies registered on and delivers on study targets, thereby contributing to the commercial success of the site
    • Reviews enrollment progress, pre-screening and screening success rates, screen failure rates, safety, and retention of participants
    • Interprets protocols and IB and participates in initiatives to strategize for patient recruitment
    • Carries out clinical evaluation and assessment of participants to ensure eligibility to enroll in studies
    • Ensures and protects the welfare and safety of participants through ethical conduct
    • Fulfills and complies with all medical duties as per protocol, SOP/COP and ICH GCP and local regulations
    • Exercises meticulous attention to detail in documentation and patient care


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