Remote Oncology Clinical Study Physician

Parexel; Trenton (NJ); Remote; USD 250,000 - 350,000; Full time

Job summary

Parexel is seeking a Clinical Study Physician for a fully remote, global role focused on oncology trials. The SP will assume medical responsibility across trial phases, ensuring high-quality medical input from protocol design through reporting.

The ideal candidate has MD training, clinical experience of 4+ years, and familiarity with ICH-GCP. Strong collaboration, medical writing input, and regulator interactions are essential in this role.

Qualifications

• MD/DO physician level with clinical training and medical degree.
• Minimum 4 years of active clinical experience in internal medicine or general practice preferred.
• Experience in pharma/CRO medical functions or pharmacovigilance is desired.

Responsibilities

• Provide medical oversight from trial design kickoff to final report.
• Contribute to protocol development, data management inputs, and risk mitigation.
• Lead medical content for CQMP, IPD decisions, and trial documentation.
• Coordinate with regulators, ethics committees, and cross-functional teams.
• Support site feasibility, patient recruitment, and program-level medical decisions.
• Engage with investigators, CROs, and sponsor teams to resolve medical questions.

Skills

Windows/MS Office

English proficiency

Interpersonal skills

Analytical skills

Presentation skills

Team collaboration

Digital literacy

Education

MD (Physician)

Medical thesis preferred

Job description

Parexel is seeking a Clinical Study Physician for a fully remote, global role focused on oncology trials. The SP will assume medical responsibility across trial phases, ensuring high-quality medical input from protocol design through reporting.

The ideal candidate has MD training, clinical experience of 4+ years, and familiarity with ICH-GCP. Strong collaboration, medical writing input, and regulator interactions are essential in this role.