Clinical Research Coordinator I

ObjectiveHealth • Jonesboro, GA

1d

About The Position

ObjectiveHealth is hiring a full-time Clinical Research Coordinator to conduct clinical research and provide direct patient care. The role supports IRB-approved clinical trial protocols, including identifying, screening, randomizing, and enrolling patients; conducting clinic visits; and maintaining study records and regulatory compliance. Coordinators may work on studies in Gastroenterology, Urology, Dermatology, and/or Oncology. The successful candidate takes ownership of assigned studies and patients, communicates promptly with leadership and coworkers, follows applicable laws and protocols, and uses company-provided technologies to work efficiently.

ObjectiveHealth is a clinical research company that uses proprietary technology to increase patient access to research trials, provide physicians with enhanced care options, and deliver clinical research enrollment metrics to pharmaceutical sponsors, with the goal of improving patient outcomes at the point of care.

Requirements

• Certification such as medical assistant (MA), phlebotomy, or similar.
• Strong desire to work directly with patients and skill in patient care.
• Ability to conduct the activities required by an IRB-approved clinical trial protocol.
• Attention to detail in data entry, regulatory compliance, study setup and maintenance, and protocol adherence.
• Strong communication skills and ability to foster relationships with the research team, principal investigators, sponsors, monitors, and others.
• Ability to stay focused while managing multiple protocols and related study responsibilities.
• Legal authorization to work in the United States; the company is not accepting work visas.

Responsibilities

• Identify, screen, randomize, and enroll patients in IRB-approved clinical trial protocols.
• Conduct clinic visits and perform or assist with direct patient care, including patient consent, physical assessments, blood draws, medication administration, and ECGs.
• Maintain accurate data entry, regulatory compliance, productive site visits, and efficient study setup and maintenance while adhering strictly to protocols.
• Manage multiple protocols, IRB responses and audit findings, adverse event (AE) and serious adverse event (SAE) tracking, and eSource materials for assigned studies.
• Take ownership of assigned studies and patients, and promptly communicate questions or issues requiring correction to leadership and coworkers.
• Learn and use company-provided technologies to improve day-to-day efficiency.
• Comply with applicable laws, regulations, and requirements of governing bodies.
• Represent and embody the company's values, mission, and initiatives.

Benefits

• Competitive compensation
• 401(k) with company match
• Career pathway for advancement within the company
• Short- and long-term disability
• Health Savings and Flexible Spending Accounts
• Health, dental, and vision insurance plans
• 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