Clinical Scientist/Sr. Clinical Scientist - Oncology - Home-based anywhere in the US - FSP

Overview

The Clinical Scientist assists the Clinical Scientist Protocol Lead and study team with the clinical and scientific conduct of clinical studies. This is a home-based role in the US, part of a full-service (FSP) engagement.

What you'll do

• Support adjudication, medical monitoring, imaging data reconciliation, preparation of meeting materials and protocol deviation management.
• Support a single study or multiple studies.
• May lead a study with limited scope (e.g., Survival Follow-up).
• Liaise with cross-functional lines as appropriate.
• Interact with internal and external stakeholders (study sites, committees, etc.) in support of clinical study objectives.
• Complete required training curriculum.
• Complete timesheets accurately as required.
• Submit expense reports as required.
• Update CV as required.
• Maintain working knowledge of and comply with Parexel processes, ICH-GCPs and other applicable requirements.

What you'll need

• Demonstrated oral and written communication skills.
• MS Office Suite experience, including Word, Excel and PowerPoint.
• Advanced Excel skills (pivot tables, v-lookups).
• Proficiency in written and spoken English.
• Oncology experience.
• Experience with adjudication support, medical monitoring, imaging data reconciliation, preparation of meeting materials, and protocol deviation management.
• Bachelor's, Master's or PhD in Life Sciences with 2+ years relevant career experience, or a Bachelor's degree with significant experience in clinical development (>5 years) if the degree is not in Life Sciences.

Nice to have

• Pharmaceutical experience (beneficial but not required).
• 2 years medical monitoring experience.

Details

• Location: United States, remote, home-based anywhere in the US.
• Willingness to travel as required for key company meetings.