Clinical Research Coordinator II - Relocate to Amarillo

Objective; Amarillo (TX); On-site; USD 52,000 - 76,000; Full time

Job summary

ObjectiveHealth is seeking a Clinical Research Coordinator II to join our patient-focused team in Amarillo, TX. The role requires coordinating IRB-approved clinical trials, direct patient care, and accurate data entry, with relocation support to Amarillo.

You'll engage with physicians, sponsors, and monitors, ensure regulatory compliance, and maintain study documentation while delivering high-quality patient outcomes in Gastroenterology, Urology, Dermatology, or Oncology trials.

Qualifications

• 3+ years of clinical research coordination experience
• Experience conducting IRB approved clinical trial protocols and patient enrollment
• Direct patient care activities including consenting, physical assessments, blood draws, ECG

Responsibilities

• Own assigned studies and patients
• Communicate promptly with leadership and coworkers
• Show up on time, every time
• Ensure compliance with governing laws and regulations
• Learn and use available technologies to improve day-to-day efficiency
• Uphold Compassion, Integrity, Collaboration, Innovation, Velocity, and Dedication

Skills

Patient care

Communication

Team player

IRB protocol

Data entry

Regulatory compliance

Site visits

eSource management

AE/SAE tracking

Therapy development

Job description

ObjectiveHealth is seeking a Clinical Research Coordinator II to join our patient-focused team in Amarillo, TX. The role requires coordinating IRB-approved clinical trials, direct patient care, and accurate data entry, with relocation support to Amarillo.

You'll engage with physicians, sponsors, and monitors, ensure regulatory compliance, and maintain study documentation while delivering high-quality patient outcomes in Gastroenterology, Urology, Dermatology, or Oncology trials.