Clinical Research Aide

Responsibilities

• Conduct study procedures, including conducting and completing screeners to determine study eligibility; verifying, enrolling, and consenting eligible participants; completing follow-ups and reminders in person and remotely, which may include study interview administration as assigned.
• Administer study assessments, such as questionnaires, and obtain biospecimens.
• Process, transport, and ship biological specimens as assigned, adhering to study protocols as defined by the study manual of procedures.
• Complete study documentation and files, such as case report forms, worksheets, and medical record notes.
• Maintain confidentiality of documents and files, ensuring compliance with HIPAA regulations.
• Affiliate with the Principal Investigator and study management to complete Regulatory and IRB edits, track changes, and update the Manual of Procedures as necessary.
• Attend weekly team meetings and routine communications with fellow team members and the Principal Investigator as needed and scheduled.
• Ensure compliance with Good Clinical Practice (GCP), HIPAA, and applicable regulatory standards through completion of relevant training certifications.
• Perform other related duties and responsibilities as assigned or requested.

Qualifications

• Bachelor's degree in psychology, public health, or a related field required.
• Conversional Spanish proficiency preferred.
• Experience with structured interviewing and field recruitment.