About Mayomi

Accelerating the Future of Healthcare.

Mayomi Research Solutions was founded with a singular mission: to advance clinical research trials on a larger scale while relentlessly prioritizing the needs of clinical trial companies and the patients they serve.

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Purpose & Direction

Bridging Scientific Innovation and Operational Excellence.

To advance clinical research on a larger scale by bridging scientific innovation with operational excellence — relentlessly prioritizing the needs of sponsors, investigators, and above all, the patients they serve.

India's Most Trusted Clinical Research Partner.

To be recognized as India's most trusted clinical research partner — delivering reliable, ethical, and impactful trial solutions that accelerate medical breakthroughs and improve patient lives across the globe.

Our Team

Leadership & Expertise.

Nearly three decades of combined experience in clinical research operations, spanning global clinical studies, site management, data management, and rigorous regulatory compliance.

Founder & Director

Rajath S

MSc Clinical Research · BSc Life Sciences

A visionary clinical research leader with 11 years of progressive, hands-on experience spanning every operational facet of clinical trial execution — from site-level coordination to global project management.

  • Project Manager 1 Year End-to-end sponsor engagement, budget governance, and cross-functional team leadership for multi-site global clinical trials.
  • Clinical Research Associate (CRA) 6 Years On-site and remote monitoring, source data verification, GCP compliance assessments, and regulatory submission support for CDSCO, FDA, and EMA submissions.
  • eTMF Indexer 2 Years Electronic Trial Master File structuring, document indexing, and quality review for global trials requiring strict TMF Reference Model alignment.
  • Clinical Research Coordinator (CRC) 2 Years Patient recruitment, informed consent, protocol compliance, and IRB/EC submissions across Phase I–IV therapeutic studies.
Co-Founder

Ranjitha K

Clinical Site Operations Specialist

A dedicated clinical operations expert with 8 years of specialized experience in site management, analytical oversight, and the institutional strengthening of clinical research facilities.

Her practice is grounded in a comprehensive understanding of site activation dynamics, principal investigator coordination, and the strategic implementation of quality management systems that ensure study sites meet and exceed sponsor expectations.

  • Site Management & Operations 8 Years Overseeing site feasibility assessments, staff training programs, IRB communication, and performance benchmarking for complex multi-center clinical trials.
  • Study Analytics & Reporting Ongoing Driving data-driven decision-making through site-level enrollment tracking, protocol deviation analysis, and regulatory submission metrics.
President

Kiran Deshpande

Clinical Research & Clinical Data Management

I have over 8 years of professional experience in Clinical Research and Clinical Data Management, supporting global Phase I–III clinical trials across diverse therapeutic areas, including oncology, efficacy, and safety studies. Throughout my career, I have worked with leading clinical research organizations, gaining comprehensive expertise in clinical trial operations, site management, data management, and regulatory compliance.

My experience spans the complete clinical trial lifecycle—from study start-up, site initiation, and subject management to data review, database lock, and study close-out. I have collaborated closely with Sponsors, CROs, investigators, and cross-functional teams to ensure the successful execution of clinical studies while maintaining the highest standards of quality and compliance with ICH-GCP and applicable regulatory guidelines.

Areas of Expertise

  • Clinical Trial Site Management
  • Clinical Research Coordination
  • Clinical Data Management
  • Regulatory and Ethics Committee Documentation
  • Site Start-up and Study Close-out
  • Patient Recruitment and Retention Support
  • Source Documentation and Query Resolution
  • Database Lock and Data Quality Management
  • Electronic Data Capture (EDC) Systems
  • Electronic Trial Master File (eTMF) Management
  • Sponsor, CRO, and Investigator Coordination
  • ICH-GCP and CDSCO Regulatory Compliance
Explore Further

Explore Our Capabilities.

Discover exactly how our operational philosophy of meticulous planning and strict regulatory compliance translates into our core service offerings.

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