Regulatory Research Assistant
Adams Clinical
•Onsite
About The Position
Adams Clinical is seeking a motivated and detail-oriented Research Assistant to join our regulatory team at our growing clinical trial site network. This entry-level role is ideal for individuals interested in starting a career in clinical research and provides the opportunity to learn the fundamentals of regulatory operations while supporting the success of our studies.
Requirements
- 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.
Nice To Haves
- Bachelor’s degree in a scientific, health-related, or administrative field preferred; equivalent experience considered.
- Prior experience in clinical research, regulatory affairs, or related field preferred but not required.
- Knowledge of ICH-GCP, FDA, and IRB regulations are desirable.
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.
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
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
Upload and Match Resume
What This Job Offers
Job Type
Full-time
Career Level
Entry Level
