Clinical Scientist - FSP

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

Key Accountabilities: May include but not limited to the following:

Clinical Trial Operational 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 lines as appropriate • May interact with internal and external stakeholders (study sites, committees, etc.) in support of clinical study objectives

Compliance with Parexel Standards • Complies with required training curriculum • Completes timesheets accurately as required • Submits expense reports as required • Updates CV as required • Maintains a working knowledge of and complies with Parexel processes, ICH-GCPs and other applicable requirements

Skills: • Demonstrated oral and written communication skills • MS Office Suite Experience Required– including Word, Excel, and Power Point

• Advanced Excel skills required (pivot tables, v-lookups) • Proficient in written and spoken English • Willingness to travel as required for key company meetings

Knowledge and Experience: • 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

Education: • Bachelors/Masters/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)

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