Clinical Scientist - FSP

ParexelSouthport, NC
1d

About The Position

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).

Requirements

  • 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
  • Pharmaceutical experience beneficial but not required
  • Experience in Oncology, ID/Vacc or General Medicine
  • 2 years medical monitoring experience preferred
  • Experience with adjudication support, medical monitoring, imaging data reconciliation preparation of meeting materials, and protocol deviation management
  • 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)

Responsibilities

  • 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
  • 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
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