Clinical Research Coordinator II

ObjectiveHealth is a clinical research company that uses proprietary technology to increase patient access to research trials, 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 Clinical Research Coordinator II 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. This role involves performing and assisting with direct patient care activities such as consenting patients, physical assessments, blood draws, medication administration, and ECG.

Responsibilities

• Take ownership of assigned studies and patients.
• Communicate promptly and effectively with leadership and coworkers regarding questions or needed corrections.
• Maintain strict compliance with laws, regulations, and requirements of all applicable governing bodies.
• Conduct all aspects of clinical trial protocols: identification, screening, randomization, and enrollment of patients, as well as clinic visits.
• Perform and assist with direct patient care activities: consenting, physical assessments, blood draws, medication administration, ECG, etc.
• Ensure clean data entry, regulatory compliance, productive site visits, efficient study setup, and strict protocol adherence.
• Track and resolve IRB responses, audit findings, AE and SAE events, and maintain eSource material for assigned studies.
• Foster relationships between the research team, PIs, sponsors, monitors, and others through expert communication.
• Learn and use provided technologies to increase efficiency in daily activities.
• Embody core values: Compassion, Integrity, Collaboration, Innovation, Velocity, and Dedication.

Requirements

• 3+ years of clinical research coordination experience.
• Strong desire to work directly with patients.
• Legal authorization to work in the U.S. (no work visas accepted).
• Ability to stay focused while managing multiple protocols and regulatory tasks.
• Experience in Gastroenterology, Urology, Dermatology, and/or Oncology is a plus.

Benefits

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