Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
JobTailor Logo

See all jobs on JobTailor

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Jefferson

Senior Clinical Research Coordinator

Jefferson

Clinical Research Coordinator overseeing clinical trials with a focus on Good Clinical Research Practice (GCP). Responsible for protocol coordination and compliance in a senior role.

Posted 6/17/2026full-timePhiladelphia • Pennsylvania • 🇺🇸 United StatesSeniorWebsite

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

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

Hard Skills
clinical trial managementdata managementbiological specimen managementprotocol coordinationregulatory document preparationfeasibility planningsubject log maintenanceexpense tracking
Soft Skills
independent workminimal supervisionorientation and trainingorganizationattention to detail
Certifications & Qualifications
SoCRA certification
Industry Keywords
Good Clinical Research Practice (GCP)clinical researchIRBpatient data management

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Works independently or with minimal supervision to oversee the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP)
  • Runs portions of clinical trials from startup to closeout, including protocol coordination (screening, recruiting, enrolling, consenting), feasibility planning, data management, biological specimen management, preparation for monitoring visits, and regulatory and/or IRB document preparation
  • Ensures all study procedures are conducted according to the protocol and applicable regulations
  • Assists with the orientation and training of new staff
  • Maintains accurate subject log, tracks expense, submits appropriate documentation to Grant Administrator on a monthly basis for payment due for visits on all studies
  • Organizes and maintains documentation of all patient data

Requirements

What you’ll need
  • Minimum High School Diploma or equivalent
  • SoCRA certification preferred and 6 years of clinical research experience, or bachelor’s degree and 2 years of clinical research experience, or master’s degree and 1 year clinical research experience

Benefits

Comp & perks
  • medical (including prescription) insurance
  • supplemental insurance
  • dental insurance
  • vision insurance
  • life and AD&D insurance
  • short- and long-term disability
  • flexible spending accounts
  • retirement plans
  • tuition assistance
  • access to tuition discounts at Thomas Jefferson University after one year of full time service or two years of part time service
  • access to medical (including prescription) insurance for all colleagues, including those who work less than part-time