Remote Oncology Clinical Study Physician

Parexel; Santa Fe (NM); Remote; USD 180,000 - 230,000; Full time

Job summary

Parexel is seeking a Clinical Study Physician for a fully remote, oncology-focused role. The physician will be medically responsible through all phases of clinical trials, from protocol input to final report, and will provide oversight to ensure patient safety and data integrity.

Experience in oncology is required for this global position. As a core member of trial teams, you will collaborate with CP, CPL, and safety physicians, contributing to trial quality plans, regulatory submissions, and

Qualifications

• MD with active clinical experience (minimum 4 years) in internal medicine or general practice preferred.
• Understanding of ICH-GCP regulations and guidance.
• Experience in pharma/BIO CRO medical functions or pharmacovigilance is advantageous.

Responsibilities

• Provide medical oversight across trials from protocol development to Clinical Trial Report.
• Lead medical content for trial documents and regulatory responses.
• Perform risk-based medical monitoring and issue escalation.
• Coordinate with trial teams, data management, and CROs to ensure data quality and patient safety.
• Contribute to site engagement and investigator training.
• Support endpoints adjudication and data safety monitoring activities.

Skills

Windows proficiency

MS Office

English proficient

Local language proficiency

Interpersonal skills

Analytical thinking

Presentation skills

Training skills

Proactive teamwork

Digital literacy

Education

Physician MD

Job description

Parexel is seeking a Clinical Study Physician for a fully remote, oncology-focused role. The physician will be medically responsible through all phases of clinical trials, from protocol input to final report, and will provide oversight to ensure patient safety and data integrity.

Experience in oncology is required for this global position. As a core member of trial teams, you will collaborate with CP, CPL, and safety physicians, contributing to trial quality plans, regulatory submissions, and