Clinical Research Assistant

Job Summary

A Clinical Research Assistant is an entry-level research position responsible for performing a variety of duties including coordinating aspects of clinical trial protocols.

Responsibilities

• Act as a liaison between providers, study representatives, and patients.
• Maintain case report forms, source documents, and regulatory documents.
• Maintain stock of supplies needed to carry out protocols.
• Pack and ship patient labs and review lab results.
• Provide patient care and collect medical information during visits.
• Initiate and participate in the informed consent process.
• Conduct thorough remote screenings and assessments to determine initial patient eligibility for participation in clinical trials, coordinating with healthcare professionals as needed to verify medical history and suitability.
• Maintain detailed and accurate records of patient interactions, recruitment efforts, and consent processes in accordance with regulatory standards and study protocols.
• Collaborate closely with interdisciplinary team members including investigators, research coordinators, healthcare providers, and administrative staff to facilitate seamless recruitment and enrollment processes.
• Adhere to all relevant regulatory guidelines, institutional policies, and ethical standards governing the conduct of screening, recruitment, and enrollment in clinical research, prioritizing patient safety, privacy, and confidentiality.
• Use employee calendars to schedule appointments for patients.
• Instruct patients regarding study protocols.
• Arrange for or perform phlebotomy.
• Perform related work as required.

Qualifications

• High School Diploma or equivalent.
• Bachelor's Degree preferred.
• 2-5 years of experience in a clinical setting is a plus.
• Phlebotomy experience/certification preferred.
• Certified Nurse Assistant Certificate and/or graduation from an accredited program for medical assistants is a plus.
• Knowledge of Good Clinical Practices for clinical research is a plus.
• Knowledge of OSHA and FDA regulations regarding clinical research a plus.
• Maintaining confidentiality is a must.
• Knowledge of medical terminology is a plus.
• Knowledge of electronic medical records and scheduling systems a plus.
• Experience in working with providers and other department staff.
• Ability to apply and modify professional research principles, methods, and techniques to provide ongoing patient care.

BENEFITS (full Time)

• Competitive salary
• Health Insurance
• Dental Insurance
• Disability Insurance
• Life insurance
• Paid Time Off
• Vision Insurance