Clinical Research Coordinator/Patient Recruitment - San Antonio, TX

Quintiles • Parsippany-Troy Hills, NJ

270d • $35 - $42

About The Position

The Clinical Research Coordinator will be responsible for coordinating clinical research studies under the supervision of a principal investigator. This role requires performing complex clinical procedures, including phlebotomy, ECG, sample collection, and vital signs monitoring. The coordinator will also engage in community outreach and ensure the well-being of study subjects while maintaining high standards of safety and care. Responsibilities include updating skills and knowledge of best practices, safeguarding subjects, and addressing concerns proactively. The position involves supporting study conduct through various tasks such as reviewing protocols, preparing study materials, recruiting volunteers, and ensuring data quality.

Requirements

• High School Diploma and 1 year of relevant work experience in clinical research.
• At least 1 year of experience in a clinical research setting preferred.
• Applicable certifications and licenses as required by regulatory bodies.
• Working knowledge of clinical trials and Good Clinical Practices (GCP).
• In-depth knowledge of protocol and study-specific operating procedures.
• Skill in carrying out required clinical procedures.
• Working knowledge of medical terminology.
• Attention to detail and ability to establish effective working relationships.

Responsibilities

• Perform phlebotomy and other complex clinical procedures on subjects.
• Coordinate clinical research studies conducted by a supervising principal investigator.
• Update and maintain skills, training, and knowledge of current best nursing practices.
• Safeguard the well-being of the subjects and maintain high standards.
• Act as a volunteer advocate and address concerns proactively.
• Assist staff in clinical coordinator practices and delivery of care.
• Report deviations from normal practice to senior staff.
• Review study protocols and participate in project meetings.
• Perform clinical set-up and preparation for studies.
• Generate volunteer instructions and prepare study-specific training materials.
• Troubleshoot study issues and assist with data quality checking.
• Recruit and screen volunteers for study inclusion.
• Orient volunteers to the study and its procedures.
• Administer and manage study drugs according to standard operating procedures.
• Collect, record, and report clinical data appropriately.
• Collaborate with the study investigator on adverse events.
• Cooperate with study monitors and follow ICH GCP guidelines.

Benefits

• Potential base pay range of $35.00-$42.00 per hour.
• Incentive plans, bonuses, and other forms of compensation may be offered.
• Health and welfare benefits.

What This Job Offers

• Job Type: Part-time
• Industry: Ambulatory Health Care Services
• Education Level: High school or GED