Clinical Research Coordinator II

Job Title: Clinical Research Coordinator II
Location: San Antonio, TX 78229
Duration: 6 Month(s)+ (Possible Extension)


Shift: Days, Monday–Friday
 
Role Summary:
Supports ongoing large clinical studies by ensuring accurate data capture, patient safety, and compliance with study protocols. Acts as a liaison between research site teams and interdepartmental staff, overseeing recruitment, enrollment, retention, data entry, and query resolution.
Key Responsibilities:

• Conduct clinical studies per FDA, GCP, and ICH guidelines.
• Provide patient care and ensure safety during study procedures.
• Schedule visits within protocol windows and maximize site capacity.
• Perform study procedures including vitals, pregnancy tests, ECGs, height, weight, and other protocol-specific activities.
• Document patient data accurately on required forms, including electronic systems (EDC, case report forms).
• Manage investigational product (IP) accountability as needed.
• Maintain IRB compliance, including approvals and ongoing requirements.
• Facilitate patient retention and positive relationships.
• Attend site initiation and other relevant training meetings.
• Assist with patient communication, bookings, and follow-ups.
• Maintain source documents, patient files, and site records.
• Adhere to company policies (COP/SCOP) and maintain a clean, safe work environment.

 
Education & Experience:

• Bachelor’s degree or equivalent in clinical/medical field.
• Valid nursing license (RN, LVN, LPN) in the operating country.
• Minimum 2+ years of relevant experience in clinical research or patient care.

 
Skills & Competencies:

• Knowledge of clinical research processes, SOPs, and safety monitoring.
• Ability to work independently with strong attention to detail and problem-solving skills.
• Good judgment, decision-making, and organizational skills.
• Strong interpersonal, communication, and teamwork skills.
• Proficient in basic computer applications and electronic data systems.