Parexel

Clinical Scientist – FSP

Parexel

full-time

Posted on:

Location Type: Remote

Location: United States

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About the role

  • Assists the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies
  • 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

Requirements

  • 2 years medical monitoring experience preferred
  • 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
  • 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)
Benefits
  • Health insurance
  • 401(k) matching
  • Flexible work arrangements
  • Paid time off
  • Professional development
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
medical monitoringclinical studiesclinical developmentdata analysisstudy management
Soft Skills
communicationcollaborationleadershiporganizational skillsstakeholder engagement
Certifications
ICH-GCP