**Parexel FSP is seeking a Clinical Scientist for a remote role in the EMEA.** 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 • Proficient in written and spoken English • Proficient in local language (as applicable) • Willingness to travel as required for key company meetings Knowledge and Experience: • Pharmaceutical experience beneficial but not required • Therapeutic Area (TA) specific experience beneficial • 2 years medical monitoring experience preferred Education: • Bachelors/Masters/PhD in Life Sciences with 2+ years relevant career experience • If no degree in Life Sciences, must have significant experience in clinical development (>5 years) EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.