Become an Investigator
Principal investigators are vital to our success in clinical research. If you’re passionate about this field, we encourage you to reach out. We’re looking to establish new investigator relationships and welcome inquiries from medical professionals and practices interested in joining the Rovia team.
Our Hybrid Site Model
The Rovia site model integrates stand-alone research centers with embedded Rovia staff in partner medical practices, enhancing patient access to clinical studies and fostering greater participation in sponsor-initiated trials. This hybrid approach provides medical practitioners with significant opportunities to advance their investigative careers. It minimizes operational burdens and financial risks for sites and investigators, enabling them to prioritize patient care. Comprehensive support is offered throughout the trial process, from sourcing and start-up to operational oversight and study conclusion, encompassing a variety of essential activities and responsibilities including:
- Turn-key support for vertical trial launches with private practices
- Dedicated team within stand-alone sites focused on rapid integration essential for optimized returns
- Managed trial logistics, both centralized and on-site
- Sub-leasing of any real estate and managing self-contained on-site staff to eliminate up-front cost outlay
- Customized Principal Investigator training, development and mentorship
- Business development, budget and contracting, patient recruitment, feasibility and other centralized services
- Study coordination staffing via pre-screeners and callers
The Rovia site model combines both stand-alone research centers and those within partnering medical practices utilizing embedded Rovia research staff. Not only does this hybrid approach provide greater access for patients to clinical studies and broader inclusion in sponsor-initiated trials, it offers outstanding opportunities for medical practitioners to advance their investigative careers.
Developed by a team of industry professionals with an acute awareness of the needs of patients, investigators, sponsors and regulators, the model’s design also reduces the operational burden and financial risk on the site and investigators, allowing optimum focus on patient care.
Services and support extends from trial sourcing and start-up through operational oversight and study conclusion, including, but not limited to the following activities and responsibilities:
- Turn-key support for vertical trial launches with private practices
- Dedicated team within stand-alone sites focused on rapid integration essential for optimized returns
- Managed trial logistics, both centralized and on-site
- Sub-leasing of any real estate and managing self-contained on-site staff to eliminate up-front cost outlay
- Customized Principal Investigator training, development and mentorship
- Business development, budget and contracting, patient recruitment, feasibility and other centralized services
- Study coordination staffing via pre-screeners and callers
Why Participate as a Clinical Trial Investigator?
- Extend access and improve health outcomes for your patients and community
- Help patients manage unmet medical needs and reduce cost of care
- Differentiate your practice in your areas of expertise
- Collaborate with peers, academic centers, sponsors and regulators
- Expand treatment options within your practice
- Add new revenue streams without operational burden or financial risk
- Ensure continued patient engagement with trusted medical providers
Ready to learn more about the Rovia Investigator Model
and how you can get involved?
Therapeutic expertise among our team of researchers, investigators and specialists is exceptional. Ranging from Allergy and Immunology, to Cardiology, Neurology, Oncology and Weight Management, Rovia’s experience encompasses virtually all medical disciplines and patient diverse populations, including geriatrics and numerous other specialties and demographics.
