US
0 suggestions are available, use up and down arrow to navigate them
PROCESSING APPLICATION
Hold tight! We’re comparing your resume to the job requirements…
ARE YOU SURE YOU WANT TO APPLY TO THIS JOB?
Based on your Resume, it doesn't look like you meet the requirements from the employer. You can still apply if you think you’re a fit.
Job Requirements of Clinical Research Coordinator II:
-
Employment Type:
Contractor
-
Location:
Atlanta, GA (Onsite)
Do you meet the requirements for this job?
Clinical Research Coordinator II
Careers Integrated Resources Inc
Atlanta, GA (Onsite)
Contractor
Job Title: Clinical Research Coordinator II
Location: Atlanta, GA 30328
Duration: 6 months+ (Possible Extension)
Shift: Days, Monday–Friday
Role Summary:
Supports a large ongoing clinical study by ensuring accurate data capture, patient safety, and compliance with study protocols. Coordinates with research site teams and interdepartmental staff throughout the study lifecycle, including recruitment, enrollment, retention, data entry, and query resolution.
Key Responsibilities:
Education & Experience:
Skills & Competencies:
Location: Atlanta, GA 30328
Duration: 6 months+ (Possible Extension)
Shift: Days, Monday–Friday
Role Summary:
Supports a large ongoing clinical study by ensuring accurate data capture, patient safety, and compliance with study protocols. Coordinates with research site teams and interdepartmental staff throughout the study lifecycle, including recruitment, enrollment, retention, data entry, and query resolution.
Key Responsibilities:
- Conduct clinical studies in compliance with FDA, GCP, and ICH guidelines.
- Provide medical care to participants while prioritizing patient safety.
- Schedule participant visits within protocol windows to maximize site efficiency.
- Perform all protocol-defined study activities (informed consent, screening, vitals, pregnancy tests, ECGs, height/weight measurements, etc.).
- Record all patient data accurately on required forms and electronic systems (EDC, case report forms).
- Maintain investigational product (IP) accountability as needed.
- Ensure IRB approvals are obtained and regulatory requirements are met throughout the study.
- Promote patient retention and build positive relationships with participants.
- Attend site initiation and protocol training meetings.
- Manage patient communications, bookings, and follow-ups.
- Maintain source documents, patient files, and site records up-to-date.
- Follow company policies (COP/SCOP) and maintain a safe, orderly work environment.
Education & Experience:
- Bachelor’s degree or equivalent in clinical/medical field.
- Valid nursing license (RN, LVN, LPN) in the operating country.
- Minimum of 2+ years relevant clinical research or patient care experience.
Skills & Competencies:
- Knowledge of clinical research processes, SOPs, informed consent, and safety monitoring.
- Ability to work independently with attention to detail and sound judgment.
- Strong organizational, decision-making, and problem-solving skills.
- Effective communication and interpersonal skills for teamwork.
- Proficiency with basic computer applications and electronic data capture systems.
Get job alerts by email.
Sign up now!
Join Our Talent Network!