Research Coordinator Jobs

About The Position

Requirements

• At least 1 year of related work experience.
• Bachelor's degree in a related field.
• Onsite clinical research coordinator experience.
• Experience coordinating oncology treatment trials.
• Experience using EPIC electronic medical record systems.
• Proficiency with Microsoft Office.
• Knowledge of medical terminology.
• Ability to occasionally lift, carry, push, and pull up to 40 pounds.
• Ability to rarely kneel, crawl, climb ladders, or handle objects over 40 pounds.

Nice To Haves

• Society of Clinical Research Associates (SOCRA) or Association of Clinical Research Professionals (ACRP) certification.

Responsibilities

• Serve as the primary contact for research participants, sponsors, and regulatory agencies.
• Coordinate moderately complex aspects of one or more clinical studies from start-up through closeout.
• Participate in sponsor monitoring meetings, monitor visits, and regulatory audits.
• Determine participant eligibility and gather consent according to the study protocol.
• Assist in developing recruitment strategies.
• Coordinate collection and processing of study specimens.
• Collect and manage patient and laboratory data and research project databases.
• Develop flow sheets and other study documents, complete case report forms, and ensure patient and research data are documented in appropriate files.
• Review and audit case report forms against source documents to ensure protocol compliance.
• Prepare regulatory submissions and complete Institutional Review Board renewals.
• Interact regularly with the principal investigator to support patient safety and proper study conduct.
• Assemble study kits for study visits and monitor procedure scheduling and charges.
• Coordinate study documents, monitor expenditures and adherence to study budgets, and resolve billing issues with finance and management staff.

Benefits

• Group medical, dental, vision, and life coverage.
• Retirement Savings Program.
• PSL.