Clinical Research Coordinator I

About the role

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. The company is seeking a qualified candidate for the full-time position of Clinical Research Coordinator.

Responsibilities

• Identify, screen, randomize, and enroll patients for IRB‑approved clinical trial protocols.
• Conduct clinic visits and perform direct patient care activities, including consenting patients, physical assessments, blood draws, medication administration, and ECG.
• Ensure acute attention to detail for clean data entry, regulatory compliance, productive site visits, efficient study set‑up and maintenance, and strict protocol adherence.
• Foster relationships with the research team, principal investigators, sponsors, monitors, and other stakeholders through expert communication.
• Advocate for company values, mission, and initiatives.
• Stay focused while managing multiple protocols, resolving and submitting IRB responses and audit findings, tracking adverse events (AE) and serious adverse events (SAE), and maintaining eSource material for assigned studies.
• Take ownership of assigned studies and patients.
• Communicate promptly and effectively with leadership and coworkers when questions arise or corrections are needed.
• Demonstrate reliability by showing up on time, every time.
• Ensure strict compliance with all applicable laws, regulations, and governing body requirements.
• Learn and use company‑provided technologies to increase day‑to‑day efficiency.
• Embrace core values of Compassion, Integrity, Collaboration, Innovation, Velocity, and Dedication.
• Contribute to the development of new therapies in gastroenterology, urology, dermatology, and/or oncology.

Requirements

• Cert