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

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

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

clinical trial managementdata managementbiological specimen managementprotocol coordinationregulatory document preparationfeasibility planningsubject log maintenanceexpense tracking

Soft Skills

independent workminimal supervisionorientation and trainingorganizationattention to detail

Certifications

SoCRA certification