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Clinical Research Physician (Early Phase Clinical Unit)

Parexel
CompanyParexel
CategoryHealthcare
LocationBaltimore
Remote
EmploymentNot stated
LevelNot stated
SalaryNot stated by the employer
First seen2 Aug 2026 (the employer did not state a posting date)
Last verified9 Aug 2026
SourceThe employer's own careers page (company_site)
Applications are handled by the employer, not by us.Apply on the employer's site →
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 LI-SM1