Clinical Research Coordinator I

ObjectiveHealth • Jonesboro, AR

8d

About The Position

ObjectiveHealth is hiring a full-time Clinical Research Coordinator to support clinical research studies and work directly with patients. The role involves conducting IRB-approved clinical trial activities, coordinating patient care and study visits, maintaining study documentation, and ensuring compliance with protocols and applicable requirements. Studies may involve Gastroenterology, Urology, Dermatology, and/or Oncology.

The coordinator is expected to take ownership of assigned studies and patients, communicate effectively with leadership and coworkers, learn and use the company’s technologies, and embody the company’s values of Compassion, Integrity, Collaboration, Innovation, Velocity, and Dedication.

Requirements

• Legal authorization to work in the United States; work visas are not currently accepted.
• Certification such as medical assistant (MA), phlebotomy, or similar is described as ideal.
• Strong desire to work directly with patients and ability to provide patient care.
• Skill in conducting clinical trial activities, including patient identification, screening, randomization, enrollment, and clinic visits.
• Ability to perform or assist with patient consent, physical assessments, blood draws, medication administration, and ECGs.
• Attention to detail in data entry, regulatory compliance, study setup and maintenance, and protocol adherence.
• Strong communication and relationship-building skills with research teams, principal investigators, sponsors, monitors, and others.
• Ability to stay focused while managing multiple protocols and related study tasks.
• Punctuality, personal accountability, teamwork, and commitment to company values.

Responsibilities

• Identify, screen, randomize, and enroll patients in IRB-approved clinical trial protocols.
• Conduct clinic visits and perform or assist with direct patient care activities, including patient consent, physical assessments, blood draws, medication administration, and ECGs.
• Maintain accurate data entry, regulatory compliance, study documentation, and strict adherence to study protocols.
• Support productive site visits and efficient study setup and maintenance.
• Manage multiple protocols, IRB responses, audit findings, adverse event and serious adverse event tracking, and eSource materials for assigned studies.
• Take ownership of assigned studies and patients, and communicate promptly with leadership and coworkers about questions or needed corrections.
• Learn and use company-provided technologies to improve day-to-day efficiency.

Benefits

• Competitive compensation
• 401(k) with company match
• Career pathway for advancement
• Short- and long-term disability
• Health Savings Accounts
• Flexible Spending Accounts
• Health insurance
• Dental insurance
• Vision insurance
• Generous paid time off
• Adoption assistance
• Paid holidays
• Other voluntary benefits

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: No Education Listed