Remote Clinical Scientist - Trial Operations

Parexel; Dover (DE); Remote; USD 90,000 - 130,000; Full time

Job summary

Parexel is seeking a Clinical Scientist to support clinical studies under the guidance of the Protocol Lead. The role involves medical monitoring, adjudication support, and preparation of materials for study oversight. Strong communication in English and MS Office proficiency are essential.

Travel is anticipated to support key company meetings and cross-site collaboration. Applicants with life sciences degrees and relevant clinical development experience are preferred.

Qualifications

• 2+ years medical monitoring experience preferred.
• TA-specific experience beneficial.
• Pharmaceutical experience beneficial but not required.

Responsibilities

• Assist the Protocol Lead and study team with the clinical/scientific conduct of clinical studies.
• Provide adjudication support, medical monitoring and data reconciliation.
• Prepare meeting materials and manage protocol deviations.
• Liaise with cross-functional teams and stakeholders to support study objectives.
• Maintain compliance with Parexel standards, ICH-GCP and applicable requirements.
• Interact with study sites, committees and other external partners as needed.

Skills

Oral and written communication

English proficiency

Willingness to travel

Education

Bachelor/Master/PhD in Life Sciences

Clinical development experience (>5 years) if no Life Sciences degree

Tools

MS Office Suite (Word, Excel, PowerPoint)

Job description

Parexel is seeking a Clinical Scientist to support clinical studies under the guidance of the Protocol Lead. The role involves medical monitoring, adjudication support, and preparation of materials for study oversight. Strong communication in English and MS Office proficiency are essential.

Travel is anticipated to support key company meetings and cross-site collaboration. Applicants with life sciences degrees and relevant clinical development experience are preferred.