Clinical Research Assistant
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About The Position
A Clinical Research Assistant is an entry-level research position responsible for performing a variety of duties related to clinical trial protocols. This includes coordinating study initiation, recruitment, study visits, monitor visits, regulatory compliance, and study close-out. The role requires acting as a liaison between providers, study representatives, and patients, ensuring effective communication and collaboration throughout the research process. The Clinical Research Assistant will maintain case report forms, source documents, and regulatory documents, ensuring that all necessary paperwork is accurate and up-to-date. Additionally, they will manage the stock of supplies needed to carry out protocols and will be responsible for packing and shipping patient labs while reviewing lab results as necessary. The Clinical Research Assistant will provide patient care and collect medical information during visits, initiating and participating in the informed consent process. They will conduct screenings of prospective study participants and schedule appointments for patients interested in research studies. Identifying potential research participant candidates will involve utilizing various channels, including medical records, databases, referrals, and community outreach. The assistant will obtain informed consent from eligible participants according to established guidelines, ensuring comprehension and compliance with ethical standards and regulatory requirements. Maintaining detailed and accurate records of patient interactions, recruitment efforts, and consent processes is crucial, as is collaborating closely with interdisciplinary team members, including investigators, research coordinators, healthcare providers, and administrative staff. The Clinical Research Assistant must 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. They will also use employee calendars to schedule appointments for patients and instruct them regarding study protocols. The role may involve arranging for or performing phlebotomy and performing related work as required.
