Clinical Research Coordinator

ObjectiveHealth • Nashville, TN

396d

About The Position

The Clinical Research Coordinator at ObjectiveHealth is responsible for managing clinical trials and ensuring compliance with regulatory requirements while providing direct patient care. This role involves patient interaction, data management, and collaboration with various stakeholders to improve patient outcomes in clinical research.

Requirements

• Certification as an RN, LPN, MA, phlebotomist, or similar.
• Prior clinical research experience.
• Strong patient care skills and a passion for patient interaction.
• Attention to detail for data entry and regulatory compliance.
• Excellent communication skills and ability to foster relationships with stakeholders.

Nice To Haves

• Experience in Gastroenterology, Urology, Dermatology, or Oncology research.
• Familiarity with clinical trial management software.

Responsibilities

• Manage assigned clinical trials from start to finish, ensuring compliance with IRB approved protocols.
• Conduct patient identification, screening, randomization, and enrollment activities.
• Perform direct patient care activities including consenting patients, physical assessments, blood draws, and medication administration.
• Maintain accurate and clean data entry for regulatory compliance and study documentation.
• Communicate effectively with research team members, principal investigators, sponsors, and monitors.
• Track adverse events (AE) and serious adverse events (SAE) and maintain eSource material for assigned studies.
• Ensure timely responses to IRB queries and audit findings.

Benefits

• Competitive compensation
• 401(k) with company match
• Short- and long-term disability insurance
• Health Savings and Flexible Spending Accounts
• Health, dental, and vision insurance plans
• Generous paid time off (PTO)
• Adoption assistance
• Paid holidays
• Voluntary benefits options

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: Associate degree