Clinical Research Physician

Parexel • Glendale, CA

8d • Onsite

About The Position

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. Bring your medical expertise to the forefront of drug development. Are you a physician interested in using your clinical expertise in a different way while still remaining closely connected to patient care? Join Parexel’s Early Phase Clinical Unit in Glendale, CA as a Clinical Research Physician and play an important role in the development of new therapies. This full-time opportunity offers the chance to work directly with study participants, clinical research teams, and sponsors in a highly collaborative environment. For physicians looking for greater predictability, the position offers day-shift hours and an attractive work-life balance, with an on-call schedule of approximately 1 out of every 6 weekends. Whether you already have clinical research experience or are looking to bring your medical background into the clinical research setting, this is an opportunity to expand your career while contributing to meaningful early-stage research.

Requirements

• MD or DO degree
• Ability to obtain and maintain an unrestricted California medical license
• Strong interpersonal and communication skills
• Detail-oriented approach with ability to work effectively in a fast-paced clinical research environment
• English language proficiency

Nice To Haves

• At least 2 years of clinical practice experience
• Board certification in a general medical specialty or equivalent experience
• Previous clinical or pharmaceutical research experience
• Familiarity with the FDA-regulated drug development process

Responsibilities

• Serve as an Investigator and execute appropriate Investigator responsibilities for assigned clinical studies.
• Provide medical and clinical oversight throughout study conduct.
• Evaluate study participants through physical examinations, medical histories, laboratory data, and inclusion/exclusion criteria.
• Provide medical consultation and clinical guidance to research staff and study sponsors.
• Review safety information, including adverse events, concomitant medications, laboratory findings, vital signs, and other clinical data.
• Assess adverse events for clinical significance, severity, seriousness, and relationship to investigational products.
• Work closely with clinical operations colleagues to ensure high-quality, efficient, and compliant study execution.
• Collaborate directly with sponsors regarding study conduct and progression.
• Support clinical protocols, reports, safety documentation, and other study-related materials.
• Help ensure studies are conducted in accordance with Good Clinical Practice (GCP), SOPs, and applicable regulatory requirements.
• Collaborate with physician colleagues and local/regional medical consultants.
• Contribute to the development and training of clinical operations team members.

Benefits

• Full-time, day-shift schedule
• Predictable on-call rotation of approximately 1 in every 6 weekends
• Opportunity to maintain meaningful physician and participant interaction
• Exposure to early-phase clinical development and investigational therapies
• Direct collaboration with sponsors, clinical operations professionals, and other physicians
• Supportive, team-oriented environment
• Opportunity to build or further develop a career within the clinical research and pharmaceutical industry

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Ph.D. or professional degree