Primary Responsibilities:

• Conduct research activities in accordance with study protocols and regulatory requirements.
• Assist with protocol development and routine research procedures.
• Coordinate and schedule study participants for research visits and follow-up activities.
• Screen, recruit, consent, and enroll participants in clinical research studies.
• Collect, enter, track, and maintain research data and study records.
• Set up, maintain, and operate research materials and equipment.
• Assist with IRB submissions and regulatory documentation.
• Support quality assurance efforts to ensure the integrity and accuracy of research data.
• Monitor compliance with safety, regulatory, and Good Clinical Practice (GCP) guidelines.
• Perform other duties as assigned.

Candidates should have strong analytical, organizational, and critical thinking skills, with a high level of attention to detail and accuracy. Experience working with clinical, scientific, or research data is required. Experience with transcriptomic, proteomic, bioinformatics, data science, or other advanced data analysis techniques is preferred.