Research Assistants (RAs) work under the direction of the Site Director and the supervision of the Clinical Research Coordinator to support the execution of clinical research studies. This is an entry-level position designed to provide hands-on exposure to clinical research operations. Research Assistants assist with study-related tasks including participant coordination, data collection, documentation, and administrative support while ensuring adherence to study protocols, Good Clinical Practice (GCP), and regulatory requirements. The role requires frequent interaction with research participants and clinical staff, strong attention to detail, and the ability to follow established procedures in a regulated environment.
Duties and Responsibilities
Assist with informing participants about study expectations and visit procedures under supervision
Prepare and organize study materials such as consent forms, questionnaires, logs, and binders
Support participant recruitment efforts by identifying and coordinating potential study subjects as directed
Assist with scheduling study visits and coordinating with clinical and research staff
Support data collection and documentation in source documents and electronic systems as assigned
Ensure study documentation is complete, accurate, and filed according to protocol and site requirements
Observe and support study procedures under appropriate supervision and training
Promptly report concerns, deviations, or incidents to the Clinical Research Coordinator or Site Director
Assist with maintaining participant confidentiality and compliance with HIPAA requirements
Support preparation for monitoring visits, audits, and inspections
Perform general administrative and operational tasks related to study conduct
Key Competencies
Strong interpersonal, written, and verbal communication skills
Ability to follow written protocols, SOPs, and regulatory guidance
Strong organizational skills and attention to detail
Ability to work collaboratively with clinical staff, coordinators, and management
Basic computer proficiency, including Word, Excel, and data entry systems
Willingness to learn clinical research regulations and procedures
Work Environment
This is a fast-paced clinical research environment that requires flexibility, attention to detail, and professionalism. Variable hours may be required to accommodate study and participant needs. Occasional travel between sites or participation in extended study days may be required.
Physical Demands
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.
Stand and walk for extended periods
Lift up to 30 pounds occasionally
Grasp, reach, and handle materials frequently
Sit with back support for extended periods
Environmental Demands and Potential Hazards
Exposure to hazards from fluorescent lighting, video screens, computers, copiers, and office equipment
Work performed within a medical or clinical setting
Potential exposure to blood, body fluids, infectious diseases, radiation, hazardous chemicals, or medications
Noise levels range from quiet to moderate
Periods of sustained focus and moderate stress consistent with clinical operations
Position may require on-call availability based on study demands and scheduling needs
Required Education and Experience
High School Diploma or equivalent
Ability to communicate effectively and professionally with providers, coworkers, participants, and sponsors
Ability to work in a regulated healthcare or research environment
Preferred Education and Experience
Associate's degree or coursework in health sciences or related field
Prior experience in healthcare, research, or customer-facing roles
Familiarity with medical terminology
Introductory knowledge of GCP, HIPAA, and clinical research principles
Other Duties
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities required for this position. Duties, responsibilities, and activities may change at any time with or without notice.
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