Senior Study Physician & Medical Lead — Remote (EMEA)

Embedded Shishya; United States; Remote; USD 180,000 - 230,000; Full time

Benefits offered by this job

Medical care plan: Health, Dental &amp

Life Assurance

Pension plan

Excellent training

Job summary

Parexel is seeking an experienced Study Physician to join our team. You will be medically responsible at the trial level across the preparation, conduct, and reporting phases, providing expert medical oversight from Trial Design Outline to the Clinical Trial Report.

We value dedicated professionals who can work with minimal supervision, ensure high-quality protocols, and manage risks through scientific insight and data-driven approaches.

Qualifications

• Physician (MD) with clinical training and a minimum of 4 years of active clinical practice.
• Specialization in Pulmonology, Immunology, Internal Medicine, Infectious Diseases, Family Medicine, Pediatrics, Rheumatology, or Emergency Medicine is desirable.
• Experience in pharma industry or CRO in medical/project management or pharmacovigilance is desirable.
• Understanding of ICH-GCP and regulatory guidance.
• Ideally previous experience as a medical monitor.
• Experience with data visualization systems and IT systems is a plus.
• Clinical development/trials experience would be an asset.

Responsibilities

• Provide medical oversight at trial level from design to Clinical Trial Report.
• Co-author Clinical Quality Monitoring plans.
• Perform ongoing reviews of medical data.
• Ensure timely preparation of high-quality clinical trial protocols, minimising amendments.

Skills

Medical expertise

Clinical monitoring

Regulatory knowledge

ICH-GCP familiarity

Education

MD (Medical Doctor)

Medical thesis (preferred)

Tools

Data visualization systems

IT systems

Job description

Parexel is seeking an experienced Study Physician to join our team. You will be medically responsible at the trial level across the preparation, conduct, and reporting phases, providing expert medical oversight from Trial Design Outline to the Clinical Trial Report.

We value dedicated professionals who can work with minimal supervision, ensure high-quality protocols, and manage risks through scientific insight and data-driven approaches.