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Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.

Clinical Research Physician (Early Phase Clinical Unit)

Job ID R0000037951 Baltimore, Maryland

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 prefered.
  • 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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