Remote Clinical Scientist, Clinical Trials & Monitoring

Parexel; Jackson (MS); On-site; USD 90,000 - 130,000; Full time

Job summary

Parexel is seeking a Clinical Scientist to assist the CS Protocol Lead and study team with the clinical and scientific conduct of clinical studies. You will support medical monitoring, data reconciliation, and preparation of meeting materials, while managing protocol deviations and coordinating with sites and committees.

The role emphasizes collaboration across functions, adherence to ICH-GCPs, and ongoing learning within Parexel's global clinical research framework.

Qualifications

• 2+ years medical monitoring or clinical trial experience preferred.
• Bachelor's/Master's/PhD in Life Sciences required.
• Therapeutic Area experience beneficial.
• Willingness to travel for meetings and site visits.

Responsibilities

• May support a single study or multiple studies.
• May lead a study with limited scope (e.g., Survival Follow-up).
• Liaises with cross-functional lines as appropriate.
• Interacts with study sites, committees and other stakeholders to support clinical objectives.

Skills

Verbal & written communication

MS Office proficiency

English proficiency

Willingness to travel

Education

Life Sciences degree

Clinical development experience alternative

Tools

MS Office (Word/Excel/PowerPoint)

Job description

Parexel is seeking a Clinical Scientist to assist the CS Protocol Lead and study team with the clinical and scientific conduct of clinical studies. You will support medical monitoring, data reconciliation, and preparation of meeting materials, while managing protocol deviations and coordinating with sites and committees.

The role emphasizes collaboration across functions, adherence to ICH-GCPs, and ongoing learning within Parexel's global clinical research framework.