Remote Oncology Study Physician - Medical Oversight Leader

Parexel; Atlanta (GA); Remote; USD 180,000 - 230,000; Full time

Job summary

Parexel FSP is seeking a Clinical Study Physician for a fully remote role focused on oncology trials. The SP is medically responsible across trial phases, providing medical oversight from protocol design to final reporting.

The role requires oncology experience and strong collaboration with global trial teams, regulatory bodies, and data management to ensure high-quality medical data and patient safety throughout the study lifecycle.

Qualifications

• MD with medical training and clinical setting experience.
• Minimum 4 years of active clinical experience; internal medicine or general practice preferred.
• Experience in pharma or CRO medical/pharmacovigilance functions is a plus.
• Understanding of ICH-GCP and regulatory requirements.

Responsibilities

• Provide medical oversight from trial design to Clinical Trial Report (CTR).
• Input into Clinical Trial Protocols (CTPs) and CQMP/IQRMP documents.
• Address medical queries from Investigators and Sponsor teams; support site feasibility and training.
• Develop and review medical content for trial documents; ensure data quality and patient safety.
• Support Endpoint Adjudication, DMC/DSMB as applicable and coordinate with global trial teams.

Skills

Windows & MS Office

Written and spoken English

Interpersonal skills

Analytical skills

Presentation skills

Teamwork

Digital literacy

Education

Physician MD degree

Internal medicine or general practice training

Tools

Data visualization systems

IT systems

Job description

Parexel FSP is seeking a Clinical Study Physician for a fully remote role focused on oncology trials. The SP is medically responsible across trial phases, providing medical oversight from protocol design to final reporting.

The role requires oncology experience and strong collaboration with global trial teams, regulatory bodies, and data management to ensure high-quality medical data and patient safety throughout the study lifecycle.