Clinical Research Coordinator II

ObjectiveHealth is a clinical research company that uses proprietary technology to increase patient access to research trials within our communities, provide physicians with enhanced care options for current patients, and deliver superior clinical research enrollment metrics to Pharma sponsors—all with the goal of improving patient outcomes at the point of care.

About the role

The ideal candidate will possess 3+ years of clinical research coordination experience and have a strong desire to work directly with patients. This full-time position involves conducting IRB-approved clinical trial protocols, performing direct patient care activities, and ensuring regulatory compliance.

Responsibilities

• Identify, screen, randomize, and enroll patients for clinical trials
• Conduct clinic visits and assist with direct patient care activities (consenting, physical assessments, blood draws, medication administration, ECG, etc.)
• Maintain strict protocol adherence and regulatory compliance
• Perform clean data entry and ensure productive site visits, efficient study set-up, and maintenance
• Track adverse events (AE) and serious adverse events (SAE), resolve and submit IRB responses and audit findings
• Maintain eSource material for assigned studies
• Communicate effectively with the research team, principal investigators (PIs), sponsors, monitors, and other stakeholders
• Take ownership of assigned studies and patients, ensuring timely and accurate completion of tasks
• Learn and utilize provided technologies to increase efficiency in daily activities
• Embody company core values: Compassion, Integrity, Collaboration, Innovation, Velocity, and Dedication

Requirements

• 3+ years of clinical research coordination experience
• Strong desire and ability to work directly with patients
• Skilled in all aspects of conducting IRB-approved clinical trial protocols
• Experience performing direct patient care activities (e.g., consenting, physical assessments, blood draws, medication administration, ECG)
• Acute attention to detail for data entry, regulatory compliance, and protocol adherence
• Excellent communication skills to foster relationships among research teams, PIs, sponsors, and monitors
• Ability to stay focused while managing multiple protocols and tasks
• Legal authorization to work in the U.S. (no work visas accepted at this time)

Skills

• Patient interaction and care
• Team collaboration with a bias for action
• Regulatory compliance and IRB processes
• Clinical trial protocol execution
• Data entry and eSource maintenance
• Multitasking and time management
• Advocacy for company values and mission
• Interest in therapy development in Gastroenterology, Urology, Dermatology, and/or Oncology

Benefits

• Competitive compensation
• 401(k) with company match
• Health, dental, and vision insurance plans
• Health Savings Account (HSA) and Flexible Spending Accounts (FSA)
• Short- and long-term disability
• Generous paid time off (PTO)
• Paid holidays
• Adoption assistance
• Wide selection of voluntary benefits
• Clear career pathway for advancement within the company