Support leading pharmaceutical companies, CROs, and medical centers by ensuring smooth clinical trial review processes.
About Advarra
Advarra is a market leader in advancing clinical research and human health. With roots in ethical review services, cutting-edge technology, and deep industry expertise, we connect patients, sites, sponsors, and CROs to accelerate trials. Our values—Patient-Centric, Ethical, Quality-Focused, and Collaborative—guide everything we do as we work to improve lives worldwide.
Schedule
- Full-time, remote (U.S.-based)
- Standard business hours with responsiveness required for client communication
What You’ll Do
- Serve as the main client contact for sponsors, CROs, and PI sites on assigned studies.
- Conduct administrative review of protocol and site submissions, ensuring requirements are met.
- Document and process client customizations and protocol change requests.
- Manage vendor relations for foreign language translations.
- Collaborate with the QA team to ensure high accuracy and minimal errors.
- Respond to client inquiries within 24 hours and escalate issues as needed.
What You Need
- 2+ years’ experience in IRB or clinical research, including applying regulations for human subject protection.
- Proficiency with MS Office (Word, Outlook) and ability to learn proprietary systems.
- Strong attention to detail and organizational skills.
Preferred
- Certified IRB Professional (CIP) credential, or willingness to obtain within one year of eligibility.
Benefits
- Salary range: $48,830 – $61,500 annually (based on experience, skills, and location)
- Eligibility for annual bonus
- Health, dental, and vision insurance
- Paid holidays and additional benefits
Make an impact on the future of clinical research while growing your career with a collaborative, mission-driven team.
Happy Hunting,
~Two Chicks…