Clinical Research Coordinator I

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 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 Clinical Research Coordinator I will work directly with patients and conduct all aspects of IRB-approved clinical trial protocols, including identification, screening, randomization, and enrollment of patients, as well as conducting clinic visits. The role involves performing and assisting with direct patient care activities such as consenting patients, physical assessments, blood draws, medication administration, and ECGs.

Responsibilities

• Take ownership of assigned studies and patients.
• Communicate promptly and effectively with leadership and coworkers regarding questions or necessary corrections.
• Ensure strict compliance with laws, regulations, and requirements of all applicable governing bodies.
• Perform patient care activities: consenting, physical assessments, blood draws, medication administration, ECG, etc.
• Maintain acute attention to detail for clean data entry, regulatory compliance, site visits, study setup, and protocol adherence.
• Track and resolve IRB responses, audit findings, adverse events (AE), and serious adverse events (SAE).
• Maintain eSource material for assigned studies.
• Foster relationships between the research team, PIs, sponsors, monitors, and others.
• Learn and use provided technologies to increase efficiency in daily activities.
• Embody core values: Compassion, Integrity, Collaboration, Innovation, Velocity, and Dedication.

Requirements

• Certification such as MA, phlebotomy, or similar.
• Strong desire to work directly with patients.
• Skilled in conducting IRB-approved clinical trial protocols.
• Ability to perform direct patient care activities.
• Acute attention to detail for data entry, regulatory compliance, and protocol adherence.
• Expert communication skills to foster relationships with research teams, PIs, sponsors, and monitors.
• Ability to stay focused while managing multiple protocols, IRB responses, audit findings, and AE/SAE tracking.
• Legal authorization to work in the U.S. (no work visas accepted).

Benefits

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