Note: The job is a remote job and is open to candidates in USA. Adams Clinical is a leading clinical trial site network committed to accelerating the development of life-changing medicines. They are seeking a motivated and detail-oriented Research Assistant to join their regulatory team, providing support in regulatory operations and ensuring compliance with various guidelines.

Responsibilities

• Provide administrative and organizational support to regulatory staff
• Assist with preparation, organization, and distribution of study-related documents
• Help maintain regulatory files and electronic systems to ensure records are accurate, complete, and audit-ready
• Support the submission process to Institutional Review Boards (IRBs), including assisting with renewals and updates
• Track staff training and certification records to ensure compliance

Skills

• Bachelor's degree in a scientific, health-related, or administrative field preferred; equivalent experience considered
• Exceptional attention to detail and outstanding organizational skills, with the ability to manage multiple priorities and meet deadlines in a fast-paced environment
• Strong organizational skills, attention to detail, and ability to manage multiple tasks simultaneously
• Prior experience in clinical research, regulatory affairs, or related field preferred but not required
• Knowledge of ICH-GCP, FDA, and IRB regulations are desirable

Benefits

• 401(k) matching
• Medical, Dental &Vision insurance
• Employee assistance program
• Flexible spending account
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Parental leave
• Professional development assistance

Company Overview