Clinical Scientist -Medical Data Review- Medical Monitor FSP

Oncology experience preferred Remote Role US or Canada 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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