When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. 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) #LI-LO1 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. Parexel is a leading global clinical research organization (CRO) providing insights-driven Clinical and Consulting solutions to the world’s life sciences industry. Leveraging deep local knowledge and a global breadth of clinical, regulatory and therapeutic expertise, our professionals worldwide work in partnership with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind — broadening access and making clinical research a care option for anyone, anywhere. Our proven track record spans 40+ years and drives us forward, advancing clinical research in healthcare’s most complex areas while harnessing innovation to drive efficiencies across every phase of the clinical development process. Our insights-driven approach, proven delivery and trusted execution are accelerating the delivery of life-changing treatments to patients — With Heart.™

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