Clinical Research Physician (Early Phase Clinical Unit)

Reposted 8 Days Ago
Be an Early Applicant
Baltimore, MD, USA
In-Office
Junior
Pharmaceutical
The Role
Provide medical oversight and serve as Investigator in early phase clinical trials, reviewing safety data, training staff, supporting protocol development, and liaising with sponsors while maintaining GCP and regulatory standards.
Summary Generated by Built In

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

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

EEO Disclaimer
Parexel is an equal opportunity employer.  Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

Skills Required

  • Minimum two years of clinical practice experience
  • Eligibility for an unrestricted medical license in the state of Maryland
  • ACLS certification
  • Board certification in Emergency or Internal Medicine
  • Clinical or pharmaceutical research experience
  • Familiarity with FDA-regulated drug development processes
  • Experience using ClinBase
  • 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

Parexel Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Parexel and has not been reviewed or approved by Parexel.

  • Healthcare Strength Health coverage is described as comprehensive, including medical, dental, vision, HSA/FSA options, and company-paid disability insurance. Descriptions often portray the package as strong or “top notch,” adding meaningful value.
  • Retirement Support Retirement offerings include a 401(k) with company matching and, in some regions, generous pension contributions. Core financial protections are emphasized as a solid part of the total rewards.
  • Leave & Time Off Breadth Time-off programs include ample PTO or flexible/unlimited RTO alongside flexible schedules and remote/hybrid options. Work-life balance support from managers is highlighted as a practical advantage.

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The Company
HQ: Raleigh, NC
20,524 Employees

What We Do

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com. Community Guidelines Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are: • Abusive, harassing or threatening to others. • Defamatory, offensive, obscene, vulgar or depicting violence. • Hateful targeting by race/ethnicity, age, color, creed, religion, gender, sexual preference or orientation, nationality or political beliefs. • Sexually explicit or pornographic. • Fraudulent, deceptive, libelous, misleading or unlawful. • Referencing criminal or illegal activity. • Spamming. We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.

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