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Clinical Research Physician (Early Phase Clinical Unit)

Parexel

RemoteFull timeMid levelPosted today
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About the role

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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