Research Assistant

Position Summary :

The Research Assistant will support the daily operations of clinical trials under the supervision of the Principal Investigator (PI) and Study Coordinator. This position involves assisting with patient visits, data entry, documentation, and maintaining compliance with study protocols and regulatory requirements.

Responsibilities

Assist with subject recruitment, screening, and scheduling of study participants.

Support the completion of informed consent procedures under supervision.

Perform vital signs, ECGs, and specimen collection (if certified or trained).

Conduct phlebotomy and sample processing for lab shipments, as applicable.

Maintain accurate and timely source documentation and data entry in EDC systems.

Organize and maintain study binders, files, and supplies

Ensure adherence to GCP, protocol, and site SOPs

Assist in query resolution and communication with sponsors, monitors, and CROs.

Support coordinators and investigators during monitoring visits and audits

Participate in site meetings, staff trainings, and ongoing protocol updates

Qualifications

Bachelor's degree in science, psychology, nursing, or a related field (preferred).

Experience in healthcare, research, or medical office settings (preferred but not required).

Phlebotomy certification or MA experience is a strong plus.

Excellent attention to detail, organization, and communication skills

Ability to work collaboratively in a fast-paced clinical environment

Proficiency in Microsoft Office and electronic data systems (EDC / CTMS) is desirable.