Clinical Research Physician (Early Phase Clinical Unit)
Parexel•Baltimore, MD
•Onsite
About The Position
Join a highly collaborative Early Phase Clinical Unit (EPCU) 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.
Requirements
- Minimum two years of clinical practice experience
- Eligibility for an unrestricted medical license in the state of Maryland.
- ACLS
Nice To Haves
- Board certification in Emergency or Internal Medicine preferred.
- Clinical or pharmaceutical research experience desirable.
- Familiarity with FDA-regulated drug development processes is beneficial.
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.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
