Research Assistant

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This individual will play a key role in assisting with clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. Responsibilities include :

• EDC Entry and Query Resolution
• Developing strong working relationships and maintaining effective communication with study team members
• Assisting with screening, recruiting, and enrollment of research subjects
• Performing patient / research participant scheduling and collecting patient / research participant history
• Coordinating follow-up care and laboratory procedures
• Adhering to an IRB-approved protocol and assisting in the informed consent process
• Supporting the safety of research subjects and coordinating protocol-related procedures
• Scheduling subject visits and procedures
• Ensuring compliance with company and Sponsor policies, SOPs, and guidelines

Qualifications include a High School Diploma and 1 year of relevant work experience in clinical research. Preferred experience includes working in a clinical research setting, knowledge of clinical trials and GCP, understanding of protocol and study-specific procedures, and applicable certifications. Skills required include carrying out clinical procedures, knowledge of medical terminology, attention to detail, and effective relationship-building. This position is not eligible for sponsorship.

Seniority level : Entry level

Employment type : Part-time

Job function : Research, Analyst, and Information Technology

Industries : Hospitals and Health Care

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