Our Leadership
Meet the visionary leaders driving Admerus Biosciences towards excellence in clinical research. Our experienced team brings decades of expertise in pharmaceutical development and regulatory compliance.
Abhiram Koppineedi
Founder & Managing Director
M.S., (Ph.D.)
Abhiram, Founder of ADMERUS, has a deep passion for pharmacology, complemented by over 21 years of marketing experience in the healthcare and pharmaceutical sectors. Establishing his own CRO facility was a lifelong dream, and his visionary leadership has been instrumental in launching several start-up CROs globally. With expertise in client relationship management, strategic planning, and drug development processes, Abhiram continues to drive innovation and growth within the company. His keen business acumen combined with a proven record are a valuable asset in effectively managing client relationships, strategic planning, and marketing. With his breadth of knowledge of drug development processes combined with his assertive and excellent people skills, Abhiram has been able to anticipate client needs while negotiating for them and leveraging existing contracts to enhance and expand businesses.
Dr. Sailendra Kumar Goswami
Chief Executive Officer & Director
B. Pharm., M. Pharm., Ph.D.
Dr. Sailendra Kumar Goswami, one of the best known experts in the field, has over 25 years of professional experience in the clinical research industry. His vast body of work includes over 3,000 bioequivalence studies, patient-based studies, in vitro BE studies, and studies for derma products for regulatory agencies including FDA (USA), Health Canada, MHRA (UK), EMA (EU), WHO, TGA (Australia), and more.
He has founded and established several clinical research organizations including Veeda Clinical Research, GVK Biosciences, and Zydus Research Centre.
Key Leadership Team
Experienced professionals leading our clinical research, quality assurance, and compliance operations
Dr. Sanjeeva Reddy K
Vice President - Clinical Research
A highly experienced ICH-GCP trained medical professional with 22+ years of expertise in Quality Assurance, Clinical Research, Clinical Development, Medical Affairs, and Pharmacovigilance. Proven track record in leading diverse activities, strategic planning, and achieving quality outcomes in fast-paced environments. Skilled in identifying organizational needs, resolving deficiencies, and delivering innovative, cost-effective solutions to ensure timely project completion. Expertise in managing audits, regulatory approvals, and compliance across global standards like GCP, GLP, and GxP, consistently driving successful outcomes in BA/BE and clinical trial operations.
Dr. Susanta Kumar Pradhan, M.S, (Ph.D.)
Associate Vice President - Quality & Compliance
A Doctorate in Pharmaceutical Science with over 22 years of experience in quality assurance for BA/BE and clinical trials (Phase I to IV), skilled in audit & inspection, people management, and technical operations. Proven expertise in designing audit programs and quality management systems, consistently securing regulatory approvals for clinical research sites. Adept at training and motivating teams to achieve performance goals while ensuring process improvements, data integrity, and GxP compliance. Successfully handled national and international regulatory audits and resolved queries with authorities like DCGI, USFDA, and MHRA, ensuring compliance and operational excellence.