Senior Clinical Research Coordinator

Care Access; Hoboken (NJ); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

PTO and Holidays

Medical, dental, and vision insurance

401(k) with company match

Relocation assistance

Job summary

Care Access in Hoboken, NJ is seeking a Clinical Research Coordinator to screen, enroll, and monitor study subjects per GCP and protocol. The role is on-site with travel expectations and involves maintaining regulatory compliance and strong participant relations.

You will coordinate visits with investigators and Sponsor/CROs, manage source documents, and assist in recruitment planning. A Bachelor's degree (preferred) and experience in clinical research are expected.

Qualifications

• Bachelor’s degree preferred or equivalent experience.
• Strong knowledge of GCP, FDA regulations and ICH guidelines.
• Excellent data entry and documentation skills.
• Proficient in MS Word and Excel; able to manage trial data.

Responsibilities

• Screen, enroll and monitor study subjects per GCP and protocol.
• Maintain regulatory compliance with FDA and ICH guidelines.
• Coordinate site visits and communicate with investigators, sponsors and staff.
• Enter data in real time and manage source documents and regulatory filings.
• Assist in recruitment planning and candidate listing.

Skills

GCP knowledge

FDA regulations

ICH guidelines

Data entry

MS Word & Excel

Verbal communication

Education

Bachelor’s degree (preferred)

Tools

Clinical trials database

IVRS/EDC systems

MS Word

MS Excel

Job description

Care Access in Hoboken, NJ is seeking a Clinical Research Coordinator to screen, enroll, and monitor study subjects per GCP and protocol. The role is on-site with travel expectations and involves maintaining regulatory compliance and strong participant relations.

You will coordinate visits with investigators and Sponsor/CROs, manage source documents, and assist in recruitment planning. A Bachelor's degree (preferred) and experience in clinical research are expected.