Clinical Scientist - FSP

About the role

The Clinical Scientist (CS) assists the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies, including adjudication support, medical monitoring, imaging data reconciliation, preparation of meeting materials, and protocol deviation management.

Responsibilities

• Support a single study or multiple studies
• 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
• Comply with Parexel Standards, including required training curriculum
• Complete timesheets and submit expense reports as required
• Maintain a working knowledge of and comply with Parexel processes, ICH-GCPs, and other applicable requirements

Skills

• Demonstrated oral and written communication skills
• Proficiency in MS Office Suite (Word, Excel, PowerPoint)
• Advanced Excel skills required (pivot tables, v-lookups)
• Proficient in written and spoken English
• Willingness to travel as required for key company meetings

Requirements

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

Qualifications

• Bachelor’s/Master’s/PhD in Life Sciences with 2+ years relevant career experience
• If no degree in Life Sciences, must have Bachelor’s degree with significant experience in clinical development (>5 years)