A practical clinical research partner
Salvera Clinical Research supports sponsors, CROs, diagnostic companies, medical device innovators and healthcare partners with practical, high-quality clinical research services — bringing together clinical operations expertise, site execution experience, regulatory understanding and patient-centered delivery to move studies from concept to completion.
Execution-focused clinical research, end to end
We understand that successful studies require more than a protocol — they require trained teams, clear workflows, fast communication and reliable data.
Salvera can support as a clinical research site, operational consultant, study startup partner or strategic advisor based on the needs of each project.
We prioritize ethical study conduct, participant education, strong documentation and a smooth patient experience.
Experienced clinical research leadership
Led by professionals with deep experience across clinical trials, site operations, CRO services, diagnostics, medical devices and regulatory-driven study execution.
Shraddha Dubal, M.D., CCRP
Dr. Shraddha Dubal brings more than 16 years of clinical research experience across pharmaceutical, biotech, diagnostic, medical device, CRO, and academic settings. Her expertise spans the full clinical trial lifecycle, from protocol development, feasibility, site selection, study start-up, regulatory strategy, monitoring oversight, data review, and sponsor/site management through study close-out. She has successfully supported and led a wide range of clinical projects, including pharmacological and therapeutic studies, CLIA-waived and point-of-care diagnostics, molecular and immunoassay studies, women’s health, respiratory, infectious disease, usability, IVD, medical device, and post-market clinical studies. Known for her strategic thinking, strong work ethic, and hands-on leadership, Dr. Dubal has built trusted relationships with sponsors, clinical sites, investigators, and industry partners. Her ability to connect the right sites with the right studies, solve operational challenges, and keep projects moving forward makes her a valuable partner for organizations looking to execute high-quality clinical research efficiently, compliantly, and successfully.
Move your study forward with clarity & confidence
Tell us about your study — startup, site operations, diagnostic or device validation — and we’ll follow up with next steps.