Senior Clinical Research Coordinator: Protocol & Data Quality

DM Clinical Research; Philadelphia (Philadelphia County); On-site; USD 60,000 - 90,000; Full time

Job summary

A clinical research organization in Philadelphia seeks a Clinical Research Coordinator III to ensure quality research at investigative sites. The ideal candidate will have over 5 years of clinical research experience and be well-versed in FDA regulations and ICH/GCP guidelines. Responsibilities include overseeing study visits, adhering to documentation standards, and maintaining knowledge of protocols. This role requires strong communication skills and the ability to mentor staff, ensuring study enrollment goals are met efficiently.

Qualifications

• Minimum of 5 years experience in Clinical Research.
• Experience in supervising preferred.
• Wide therapeutic range of clinical trials experience preferred.

Responsibilities

• Conducting and overseeing study subject visits and documenting.
• Adherence to ALCOA-C Standards with clinical trial documentation.
• Maintaining a working knowledge of FDA regulations and ICH-GCP guidelines.

Skills

Detail-oriented

Proactive

Strong written communication

Excellent customer service skills

Education

High School Diploma or equivalent

Bachelor's degree

Foreign Medical Graduates

Tools

ACRP certification

Job description

A clinical research organization in Philadelphia seeks a Clinical Research Coordinator III to ensure quality research at investigative sites. The ideal candidate will have over 5 years of clinical research experience and be well-versed in FDA regulations and ICH/GCP guidelines. Responsibilities include overseeing study visits, adhering to documentation standards, and maintaining knowledge of protocols. This role requires strong communication skills and the ability to mentor staff, ensuring study enrollment goals are met efficiently.