Clinical Scientist - FSP
# Clinical Scientist - FSP **Parexel** · United States · `Remote` · `Full Time` 💼 **Уровень роли:** `Mid-level` 🕒 **Статус:** *Опубликовано: сегодня* · *Источник: Himalayas (JSON API)* --- ### Top Skills & Match 🎯 **Ключевой стек роли:** `[Clinical-Scientist]` `[Medical-Monitor]` `[Clinical-Research-Associate]` `[Clinical-Study-Manager]` `[Clinical-Research-Coordinator]` `[Clinical-Science-Specialist]` `[Clinical-Research-Scientist]` --- ### About the Role 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. Oncology experience preferred 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) Originally posted on Himalayas
- Clinical-Scientist
- Medical-Monitor
- Clinical-Research-Associate
- Clinical-Study-Manager
- Clinical-Research-Coordinator
- Clinical-Science-Specialist
- Clinical-Research-Scientist
Наблюдалась 2026-10-02, впервые 2026-10-02, источник — Himalayas (JSON API).