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Clinical Research Coordinator/Patient Recruitment - San Antonio, Tx

1+ years
$35.00-$42.00 per hour
10 April 29, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Clinical Research Coordinator/Patient Recruitment
Location: San Antonio, Texas
Job ID: R1479961
Job Type: Part Time


Job Overview:

The Clinical Research Coordinator will work closely with the principal investigator to coordinate clinical research studies. The role involves clinical procedures, patient recruitment, and data management while ensuring the safety and well-being of study volunteers. This position is on-site and requires the completion of tasks related to study protocol, patient care, and community outreach.


Responsibilities:

  • Clinical Procedures: Perform various clinical tasks such as ECGs, sample collection (spirometry), and vital signs monitoring.

  • Study Coordination: Assist the principal investigator in the coordination of clinical research studies.

  • Patient Safety: Maintain a safe environment, advocate for volunteers, and address concerns proactively.

  • Study Support: Review study protocols and case report forms, participate in project meetings, and prepare materials for study procedures.

  • Volunteer Recruitment: Recruit and screen volunteers for the study and orient them to the study process, procedures, and visit timelines.

  • Data Management: Collect and report clinical data, assist in data quality checks, and ensure accuracy and completeness.

  • Compliance: Follow ICH GCP guidelines and assist in managing study drug administration and monitoring adverse events.

  • Community Outreach: Engage in outreach efforts to increase patient participation and enhance study enrollment.


Qualifications:

  • Education: High School Diploma required, with 1+ years of relevant work experience in clinical research.

  • Experience: At least 1 year in a clinical research setting preferred.

  • Certifications: Relevant certifications and licenses as required.

  • Skills: Ability to perform clinical procedures, work with medical terminology, and maintain attention to detail.

  • Regulatory Knowledge: Familiarity with Good Clinical Practices (GCP) and study-specific operating procedures.


Compensation:

  • Hourly Rate: $35.00 - $42.00 per hour (Based on experience and qualifications).

  • Additional benefits, including incentives, bonuses, and health/welfare plans, may be offered.


About IQVIA:
IQVIA is a leading provider of clinical research services, helping to accelerate the development and commercialization of medical treatments to improve patient outcomes.

Visit Careers at IQVIA


Equal Opportunity Employer:
IQVIA is an equal opportunity employer, providing fair consideration to all applicants.