Location: Fairfax
Position type: Full-time /Non-Exempt
$21.00 - $25.00/hr.
The Clinical Research Assistant p lays a pivotal role in ensuring the smooth execution of clinical trials conducted at our site. As a vital member of our research team, you will assist in the coordination and management of clinical research studies, ensuring adherence to protocols and regulatory requirements
Roles and Responsibilities:
Coll aborate with the Clinical Research Coordinator to oversee the planning, implementation, and completion of clinical research studies. Assist in the recruitment, screening, and enrollment of study participants, ensuring compliance with eligibility criteria. Maintain accurate and complete study documentation, including regulatory documents, study protocols, and participant records. Coordinate study visits and procedures, including scheduling participant appointments, arranging study-related tests and assessments, and ensuring timely completion of study activities. Communicate with study participants, healthcare providers, and other research staff to provide support and ensure study procedures are carried out effectively. Assist in the collection, entry, and management of study data, ensuring data integrity and confidentiality. Assist in the preparation and submission of regulatory documents to regulatory authorities and institutional review boards (IRBs). Participate in study team meetings, training sessions, and quality assurance activities as required. Maintain current knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements governing clinical research. Skill Requirements and Qualifications:
Bachelor's degree in a relevant field (e.g., life sciences, health sciences, nursing) preferred. Prior experience in clinical research or healthcare-related field is advantageous. Strong organizational skills and attention to detail. Excellent interpersonal and communication skills, with the ability to interact effectively with diverse stakeholders. Proficiency in Microsoft Office applications (Word, Excel, PowerPoint, Outlook). Ability to work independently and collaboratively in a dynamic and fast-paced environment. Knowledge of regulatory requirements and guidelines governing clinical research (e.g., ICH-GCP, FDA regulations) is desirable. EMR experience, (EPIC a plus) and Microsoft Excel, Word, and Outlook. Detailed oriented, excellent written and verbal communication skills. Excellent time management skills, team player with the ability to work independently.
