Dynamic Clinical Research Coordinator - Multi-Site Trials

ActivMed Practices & Research, LLC.

Katy (TX)

On-site

USD 42,000 - 64,000

Full time

4 days ago
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Benefits offered by this job

Medical insurance
Dental insurance
Vision insurance
Life insurance
Short-term disability insurance
Long-term disability insurance
Health savings accounts
Supplemental insurances
401k plan with safe harbor match

Job summary

Alcanza Clinical Research is seeking a Clinical Research Coordinator (CRC) to ensure study execution in compliance with GCP, ICH, HIPAA, FDA regulations, and SOPs. Responsibilities include screening patients, obtaining consent, coordinating visits, data entry in EDC, and maintaining source documentation.

The role requires a Medical Assistant diploma or related credential with at least 1 year of clinical research/clinical experience, and bilingual English/Spanish is a plus.

Qualifications

  • Minimum 1 year of clinical research or clinical experience required.
  • Proficiency with basic clinical procedures (blood pressure, vitals, EKGs, phlebotomy).
  • Bi-lingual (English/Spanish) proficiency is a plus.

Responsibilities

  • Screening patients for study enrollment.
  • Obtaining informed consent from patients.
  • Conducting patient follow-up visits and scheduling.
  • Entering data in EDC and responding to queries.
  • Maintaining logs and source documentation.
  • Monitoring visits and ensuring investigator oversight.

Skills

Microsoft applications
Electronic health records
Typing 40+ wpm
Verbal and written communication
Organizational skills
HIPAA compliance

Education

Medical Assistant diploma
LPN/LVN
EMT credential
Associate’s degree

Job description

Alcanza Clinical Research is seeking a Clinical Research Coordinator (CRC) to ensure study execution in compliance with GCP, ICH, HIPAA, FDA regulations, and SOPs. Responsibilities include screening patients, obtaining consent, coordinating visits, data entry in EDC, and maintaining source documentation.

The role requires a Medical Assistant diploma or related credential with at least 1 year of clinical research/clinical experience, and bilingual English/Spanish is a plus.

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