Remote Senior Clinical Scientist Oncology Monitoring

Parexel; Madison (WI); On-site; USD 90,000 - 120,000; Full time

Job summary

Parexel in the United States seeks a Clinical Scientist to assist the Protocol Lead and study team with the clinical and scientific conduct of clinical studies, including adjudication support, medical monitoring, imaging data reconciliation, and meeting materials preparation.

The role involves collaboration with cross-functional teams and external stakeholders to ensure study objectives are met and Parexel standards are followed.

Qualifications

• Pharmaceutical experience is beneficial but not required.
• Oncology experience is required.
• 2 years medical monitoring experience preferred.
• Experience with adjudication support, medical monitoring, imaging data reconciliation and protocol deviation management.

Responsibilities

• Clinical trial delivery: may support a single study or multiple studies.
• May lead a study with limited scope (e.g., Survival Follow-up).
• Liaises with cross-functional teams and external stakeholders.
• Supports study objectives through medical monitoring and data reconciliation.

Skills

Oral and written communication

MS Office (Word, Excel, PowerPoint)

Advanced Excel (Pivot Tables, VLOOKUPs

English proficiency

Willingness to travel

Education

Life Sciences degree (BS/MS/PhD)

Bachelor's with significant clinical development experience (>5 years)

Job description

Parexel in the United States seeks a Clinical Scientist to assist the Protocol Lead and study team with the clinical and scientific conduct of clinical studies, including adjudication support, medical monitoring, imaging data reconciliation, and meeting materials preparation.

The role involves collaboration with cross-functional teams and external stakeholders to ensure study objectives are met and Parexel standards are followed.