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
Adams Clinical is a Massachusetts research center that specializes in late-phase psychiatric and neurologic clinical trials. It was founded in 2011, and is headquartered in Watertown, Massachusetts, USA, with a workforce of 201-500 employees. Its website is https://www.adamsclinical.com/.