Professional Services
Clinical Research Staffing
Enhance your research operations with Advarra’s specialized staffing solutions, providing experienced professionals to support your clinical research and technology needs.
Key Resources
- Experts aligned with your goals and priorities
- Specialization in interacting with research participants
- Short- or long-term engagement, on-site or remote
- Flexible engagements to meet your needs
Our Expertise Is Your Advantage
Comprehensive Staffing Solutions
We provide highly qualified clinical research professionals who can fill critical interim roles and integrate seamlessly in your research supporting clinical research operations and regulatory affairs.
Research Administration
Advarra provides skilled professionals, including HRPP Directors, IRB Directors, Managers, Analysts, Coordinators, Educators, IRB Members, VPs of Research Administration, and Directors of Research Finance, to ensure seamless management of your research programs.
Research Compliance
Staffing includes experts like HIPAA Research Privacy Officers, Research Compliance Officers, Conflicts of Interest Officers, Research Integrity Officers (RIO), and Clinical Trial Billing Specialists to maintain compliance with complex regulations and ethical standards.
Research Operations
Support for roles such as Directors of Clinical Operations, Clinical Research Coordinators, Regulatory Coordinators, Clinical Research Nurses, Project Managers, Data Specialists, Study Activation Coordinators, and Quality Assurance Specialists to enhance operational efficiency.
Technology Project Support
Experts to assist with new system implementations, workflow optimization, end-user training, functionality rollouts, and software upgrades, ensuring your research technology systems run smoothly.
Manage all activities necessary
for the clinical research process:
- Ensure rapid study activation
- Eligibility screens
- Obtain informed consent
- Coordinate research
- Create and maintain study source documentation
- Manage research data entry and quality
- Submit and maintain required regulatory documents
- Engage with research sponsors
- Close-out activities
