Clinical Research Coordinator II — Generous PTO & 401(k)

ObjectiveHealth

Amarillo (TX)

On-site

USD 55,000 - 75,000

Full time

Just now
Be an early applicant
Application generator

Stand out for this role — generate a tailored resume and cover letter in about a minute.

Get past ATS filters

Benefits offered by this job

401(k) with company match
Health insurance
Paid holidays
Disability coverage

Job summary

ObjectiveHealth, a clinical research company, is seeking a Clinical Research Coordinator II to join our team in a full-time role. The ideal candidate will have 3+ years of clinical research coordination experience and a strong desire to work directly with patients.

Responsibilities include screening, enrollment, and conducting clinic visits under IRB-approved protocols, with attention to data integrity and regulatory compliance.

Qualifications

  • 3+ years of clinical research coordination experience.
  • Experience with IRB approved protocols, patient screening, enrollment.
  • Strong data entry accuracy and regulatory compliance.

Responsibilities

  • Own assigned studies and patients.
  • Screen, enroll, and conduct clinic visits per protocol.
  • Maintain accurate data entry and regulatory records.
  • Collaborate with PIs, monitors, and sponsors to ensure trial success.

Skills

Patient care
IRB protocol execution
Data entry accuracy
Regulatory compliance
Communication

Job description

ObjectiveHealth, a clinical research company, is seeking a Clinical Research Coordinator II to join our team in a full-time role. The ideal candidate will have 3+ years of clinical research coordination experience and a strong desire to work directly with patients.

Responsibilities include screening, enrollment, and conducting clinic visits under IRB-approved protocols, with attention to data integrity and regulatory compliance.

Get your free, confidential resume review.
or drag and drop your file here.