Remote Clinical Scientist - Study Operations & Monitoring

Parexel; Providence (RI); On-site; USD 90,000 - 130,000; Full time

Job summary

Parexel is seeking a Clinical Scientist to assist the clinical and scientific conduct of studies, including adjudication support, medical monitoring, and preparation of meeting materials.

You will collaborate with the study team, liaise with sites and committees, and uphold Parexel processes, ICH-GCPs, and regulatory requirements. Strong communication and English proficiency are essential; travel to key meetings may be required.

Qualifications

• Bachelor/Master/PhD in Life Sciences with 2+ years relevant career experience.
• If no degree in Life Sciences, must have significant experience in clinical development (>5 years).
• MS Office Suite (Word, Excel, PowerPoint) and strong communication skills are required.

Responsibilities

• Support clinical studies under guidance of the Protocol Lead and study team.
• Provide medical monitoring and adjudication support as needed.
• Maintain compliance with Parexel standards, ICH-GCPs and internal processes.
• Coordinate with sites and committees and prepare meeting materials.

Skills

Oral & written communication

MS Office (Word, Excel, PowerPoint)

English proficiency

Local language proficiency

Travel willingness

Education

Life sciences degree (BSc/MSc/PhD)

Clinical development experience (>5 years) if no life sciences degree

Job description

Parexel is seeking a Clinical Scientist to assist the clinical and scientific conduct of studies, including adjudication support, medical monitoring, and preparation of meeting materials.

You will collaborate with the study team, liaise with sites and committees, and uphold Parexel processes, ICH-GCPs, and regulatory requirements. Strong communication and English proficiency are essential; travel to key meetings may be required.