Job Details

Metric Bio backed with a private equity backed Clinical Site Network who are growing rapidly!

They are seeking a Clinical Research Coordinator (CRC) responsible for coordinating and managing clinical trials and research studies in accordance with regulatory requirements, study protocols, and institutional policies. The CRC will work closely with investigators, sponsors, and study participants to ensure the ethical and accurate collection of data and the integrity of the research process.

Key Responsibilities:

• Coordinate day-to-day clinical trial activities and ensure compliance with the study protocol, Good Clinical Practice (GCP), and regulatory guidelines.
• Recruit, screen, and enroll study participants; obtain informed consent.
• Schedule and conduct study visits, collect and enter data accurately into electronic databases or case report forms.
• Manage study documentation including regulatory binders, source documentation, and adverse event logs.
• Act as liaison between study sponsors, monitors, investigators, and participants.
• Prepare for and participate in monitoring visits, audits, and inspections.
• Ensure proper handling, storage, and accountability of investigational products.
• Maintain IRB submissions and updates (initial submissions, amendments, continuing reviews).
• Educate participants on study procedures, risks, and benefits.
• Track study progress, enrollment, and data collection milestones.
• Assist with budget preparation and study billing compliance as needed.

Qualifications:

Required:

• Bachelor's degree in a health or science-related field (Nursing, Public Health, Biology, etc.).
• 1–2 years of experience in clinical research or a related healthcare setting.
• Knowledge of clinical research regulations and GCP.
• Strong organizational and communication skills.
• Proficient in Microsoft Office and electronic data capture systems.

Preferred:

• Certification through ACRP (CCRC) or SOCRA (CCRP).
• Experience with IRB submissions and sponsor communications.
• Familiarity with EPIC or other electronic health record systems.

Working Conditions:

• Office and clinical environment.
• May require occasional evening or weekend hours depending on study needs.
• Occasional travel for meetings or training.