Skip to main content
ResumeKart
← Back to Jobs

Clinical Trial Associate / Senior Project Specialist - East Coast US - FSP

Parexelβ€’United Statesβ€’πŸŒ Remote
Full-timeMid Level
πŸ‘οΈ 0 viewsβ€’πŸ“ 0 applicationsβ€’Posted 9/15/2026β€’Expires 11/14/2026
Tailor Resume for This JobCheck ATS Score

Get alerts for roles like this

More Clinical Trial Associate / Senior Project Specialist - East Coast US - FSP roles in United States β€” straight to your inbox. No account needed.

Applying to this role? Tailor your rΓ©sumΓ© to this job description in one click, then download it free β€” just a small ResumeKart footer, no subscription.

Job Description

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. Candidates must be East Coast US based.

Job Summary

The Clinical Trial Associate (CTA) provides operational and administrative support to clinical trials throughout their lifecycle, ensuring consistency with applicable regulatory guidelines (ICH-GCP, client SOPs) and facilitates smooth execution of trial activities.

Study management activities may include maintenance of information databases and trial tracking reports, coordination of clinical trial documentation and general support to ensure the successful and timely execution of clinical activities and deliverables.

Key Responsibilities

Assist with organizing, updating and maintaining tracking systems and tools to support the conduct of clinical study from start-up to closeout Assist with the coordination and development of study management tools, monitoring tools, study manuals and training materials and presentations Schedule meetings, prepare and distribute meeting agendas, minutes, and follow-up action items for study teams Set up, organize and maintain study files and shared spaces in accordance with study requirements Coordinate and track study training Manage study sample and supply tracking and support interactions with vendors as needed Support the Study Management team with specific projects Effectively communicate with study team members and in collaboration with the study team, identifies and addresses study-related issues Perform routine quality checks on trial l

Required Skills

clinical trial managementregulatory guidelinesICH-GCPstudy management toolstracking systemsmeeting coordinationstudy documentationquality checksvendor managementtraining materials developmentproject supportcommunication

Partner picks for Clinical Trial Associate / Senior Project Specialist - East Coast US - FSP in United States

Matched to the skills this page calls for and the candidate's location.

Partner
  • Partner course provider

    Certification training in cloud, data, cyber security, project management and digital marketing.

  • edXVerified partner
    Partner course provider

    Courses and programmes from universities and institutions worldwide.

Partners are ResumeKart affiliates or institutes it works with; ResumeKart may earn a commission when a candidate enrols. Placement is decided by relevance, not payment. How ResumeKart earns

The best-paying roles in your field. Every week. Free.

Get job alerts and salary insights in your inbox

We respect your privacy. Unsubscribe anytime with one click.