Clinical Research Physician (Early Phase Clinical Unit)

Parexel

$175K — $210K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 2+ years clinical practice experience; board certification in Emergency or Internal Medicine preferred.
  • Clinical or pharmaceutical research experience is desirable.
  • Eligibility for unrestricted medical license in Maryland.
  • Familiarity with FDA drug development processes beneficial.
  • ACLS certification required.

Responsibilities

  • Serve as Investigator on studies, ensuring compliance with protocols and regulations.
  • Support ClinBase™ implementation within the EPCU.
  • Uphold GCP, SOPs, and internal quality standards.
  • Assist in medical oversight and training of EPCU clinical staff.
  • Review lab data and conduct patient assessments for study eligibility.
  • Provide medical consultation to sponsors and EPCU staff as required.
  • Contribute to the development of clinical protocols and reports.

Benefits

  • Full-time onsite position in Baltimore, MD.
  • Monday-Friday daytime hours with weekend on-call every 3-4 weekends.
  • Opportunity to collaborate with cross-functional teams and engage with sponsors.
Full Job Description
Clinical Research Physician - Early Phase Clinical Unit (EPCU)

Location: Baltimore, Maryland

Join a highly collaborative Early Phase Clinical Unit at the forefront of innovative therapies. We are seeking a team-oriented Clinical Research Physician who thrives in a fast-paced, highly specialized research environment and is passionate about mentoring and supporting clinical staff. This role offers the opportunity to contribute to clinical research, collaborate with cross-functional teams and engage directly with sponsors and partners.

Schedule
  • Full time, onsite in Baltimore, MD
  • Monday - Friday; daytime hours
  • Weekend On Call: Every 3-4 weekends


Key Responsibilities
  • Serve as Investigator on assigned studies, ensuring all responsibilities are executed in alignment with protocol and regulatory requirements.
  • Support the implementation and use of ClinBase™ within the EPCU.
  • Uphold Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), and internal quality standards.
  • Assist in medical and clinical oversight of EPCU operations, including training and performance input for clinical staff.
  • Review laboratory data, conduct physical assessments, obtain medical histories, and evaluate inclusion/exclusion criteria for study participants.
  • Participate in the review and coding of adverse events and concomitant medications.
  • Provide medical consultation to sponsors, clients, and EPCU staff as needed.
  • Contribute to the development and review of clinical protocols, study reports, and related documentation.
  • Participate in the EPCU physician on-call rotation and general coverage schedule.
  • Build and maintain strong working relationships with sponsors, clients, MedStar Health staff, and external medical consultants.
  • Review safety data-including adverse events, labs, and vital signs-to identify trends and ensure appropriate follow-up.
  • Support preparation of safety reports for regulatory agencies and sponsors.
  • Ensure timelines and quality standards for assigned projects are consistently met.

Skills & Attributes
  • Strong leadership, mentoring and communication skills.
  • Strong attention to detail and ability to work efficiently in a fast-paced environment.
  • Sound clinical judgment and ethical decision-making.
  • Ability to manage multiple tasks and collaborate effectively across teams.

Knowledge & Experience
  • Minimum two years of clinical practice experience; board certification in Emergency or Internal Medicine preferred.
  • Clinical or pharmaceutical research experience desirable.
  • Eligibility for an unrestricted medical license in the state of Maryland.
  • Familiarity with FDA-regulated drug development processes is beneficial.
  • ACLS


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