Clinical Research Coordinator II — Drive Quality Trials

DM Clinical Research; Philadelphia (Philadelphia County); On-site; USD 55,000 - 75,000; Full time

Job summary

A clinical research organization in Philadelphia is seeking a Clinical Research Coordinator II to ensure quality research while adhering to regulatory standards. Responsibilities include managing study subject visits, maintaining compliance with FDA regulations, and achieving enrollment goals. The ideal candidate will have at least 2 years of CRC experience, knowledge of ICH-GCP guidelines, and a preferred bachelor’s degree. Join a fast-paced environment committed to delivering high-quality data and results.

Qualifications

• At least 2 years of experience as a CRC in industry-sponsored vaccines.
• ACRP or equivalent certification preferred.
• Strong understanding of FDA regulations and ICH-GCP guidelines.

Responsibilities

• Ensure quality research and data at investigative sites.
• Conduct study subject visits and documentation.
• Liaise with clinical investigators and sponsor representatives.
• Adhere to ALCOA-C Standards in clinical trial documentation.
• Manage adverse event reporting and follow up on action items.

Skills

Detail-oriented

Goals-driven

Ability to multi-task

Energetic

Education

High School Diploma or equivalent

Bachelor's degree

Foreign Medical Graduates

Tools

EDC systems

Laboratory Manuals

Job description

A clinical research organization in Philadelphia is seeking a Clinical Research Coordinator II to ensure quality research while adhering to regulatory standards. Responsibilities include managing study subject visits, maintaining compliance with FDA regulations, and achieving enrollment goals. The ideal candidate will have at least 2 years of CRC experience, knowledge of ICH-GCP guidelines, and a preferred bachelor’s degree. Join a fast-paced environment committed to delivering high-quality data and results.