Job Title: Research Assistant

Work Set-Up: On-site
Scheduled Weekly Hours: 20 Hours

Job Profile Summary:

We are seeking a detail-oriented Research Assistant to support clinical trial activities in compliance with all applicable regulations. This role requires strong organizational skills, logical thinking, adaptability, and excellent interpersonal and team-building abilities.

Key Responsibilities:

• EDC entry and query resolution
• Maintain regulatory binder and ensure compliance with documentation standards
• Schedule and coordinate subject visits and procedures
• Develop strong working relationships and maintain effective communication with study team members
• Build trust and respect with investigators and office staff
• Assist with screening, recruiting, and enrolling research subjects
• Perform patient/research participant scheduling and collect history
• Coordinate follow-up care and laboratory procedures
• Adhere to IRB-approved protocols and assist in informed consent processes
• Support the safety of research subjects
• Comply with company and Sponsor policies, SOPs, and guidelines

Qualifications:

• Minimum of an associate’s degree or equivalent education and experience
• At least 1 year of experience in a clinical research setting preferred
• Working knowledge of clinical trials and Good Clinical Practices (GCP)
• Familiarity with protocol-specific procedures, consent forms, and study schedules
• Proficiency in EDC entry and query resolution
• Experience in visit scheduling and regulatory binder upkeep
• Strong attention to detail and ability to prioritize tasks
• Excellent communication and relationship-building skills
• Applicable certifications and licenses as required by company, state, or regulatory bodies

Please note: This position is not eligible for sponsorship.

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