Mr. Vasudev Sureddy is Head Business Development at Jeevan, has nearly 11 years of experience in Clinical Research. Vasudev is a highly committed and responsible individual with excellent communication and leadership skills. He has unmatched abilities in project management and has shown exceptional operational excellence.
He has immense energy and capability to deal with people and environment. He is a good team player and has shown the ability to consistently achieve top-notch results. Before joining Jeevan, he was associated with Veeda Clinical Research in Clinical Operations and Business Development for almost 10 years..
He has hands on experience in clinical operations and project management and worked on Glucose Clamping Techniques and Phase 1 studies in India and UK. He was earlier associated with prestigious organizations including GVK bio and Granules India Limited. Vasudev holds a Master's Degree in Pharmacy..
Mr. Jayadev Sureddi is Head Clinical Operations and Pharmacovigilance at Jeevan. He is a proven relationship-builder with unsurpassed interpersonal skills. His professional strengths include cultural sensitivity and an ability to build rapport with a diverse workforce in multicultural settings, Resourceful team player who excels at building trusting relationships with customers and colleagues.
Throughout his 12 year diversified career since 2001, he held challenging roles of increasing responsibilities in different functional areas (Sales & Marketing, Clinical Operations, Resourcing for CT operations, Project Management, Regulatory & Compliance). Prior to joining Jeevan, he served as Regulatory and Compliance Analyst at community Pharmacies in USA. As GVK Bio CPU’s Manager- Clinical Operations in 2009, he was responsible for day-to-day operations and to represent clinical research unit, PK & Biostatistical departments during regulatory / sponsor audits. As Project Manager for Veeda Clinical Research Ltd., he was responsible for developing clinical study designs, execution and timely delivery of projects. In 2006, his services were extended to Plymouth, UK unit where he was involved in clinical trial execution, Project Management and Resourcing. He also helped establishing renal function unit for the company. Earlier in his career, Jayadev played a vital role in development/growth of CRO’s like GVK Biosciences Pvt. Ltd. and Veeda Clinical Research Pvt. Ltd.
Jayadev earned his post graduate degree in Pharmacy from The Tamil Nadu Dr. M.G.R. Medical University, from the department of Pharmacology, J.S.S. College of Pharmacy, Ooty and his bachelor degree from the Bangalore University.
Mr. Naidu is the Head of Quality Assurance at Jeevan. He is responsible for management of Quality Assurance unit while maintaining compliance and adherence to high standards of quality in line with international quality standards at Jeevan. He is also responsible for regulatory submissions and handling of regulatory inspections. Naidu has over 15 years of extensive experience in design and implementation of QMS policies & procedures, audit programs (internal/external), SOPs and STPs. He also has rich professional experience in handling various regulatory inspections and their queries like; USFDA, ANVISA, MHRA, MoH Turkey, NPCB, CAP, NABL and DCGI. Earlier Naidu was associated with Azidus laboratory as Head of Quality Assurance, Actimus Biosciences as General Manager and RA Chem Pharma as Head of Bioanalytical department and holds a Master's degree in Pharmaceutical analysis from Dr. MGR university- Chennai.
Mr. Sunil Kumar is the Head of Bioanalytical department at Jeevan. He is currently supervising a research professional team involved in method development, method validationand also ensures compliance to the system and implementation of automation and innovation and cost effective approach in department.
Previously he worked with major CROs like Veeda and GVK Bio with a vast and diverse experience of over 10 years in bioanalytical research. Mr. Sunil has successfully faced several audits and inspections from leading regulatory bodies like USFDA, ANVISA, UK MHRA, MOH, WHO and others. Previously he worked with major CROs like Veeda and GVK Bio with a vast and diverse experience of over 10 years in bioanalytical research. Mr. Sunil has successfully faced several audits and inspections from leading regulatory bodies like USFDA, ANVISA, UK MHRA, MOH, WHO and others..
He has hands on experience of handling different complex molecules using various analytical instruments like LC-MS, HPLC. Mr. Sunil holds a Masters degree in Biotechnology from Periyar University Salem..
Dr. Kiran Kishore is the Clinical Pharmacologist at Jeevan. Dr. Kiran is responsible for development of trial protocols, execution and medical monitoring of Clinical Operations conducted by Jeevan. He provides medical support to Pharmacovigilance, Medical Writing and Regulatory Affairs projects at Jeevan.
Prior to joining Jeevan, Dr. Kiran worked as a Principal Investigator for Clinical studies conducted at Nizam’s Institute of Medical Sciences (NIMS) during his tenure of DM course in Clinical Pharmacology & Therapeutics. He also worked as an Assistant Professor in the Department of Pharmacology at Mamata Medical College and Bhaskar Medical College. He has more than 12 publications in indexed journals which include original research articles, case reports and reviews.
Dr. Kiran did his DM (Doctorate of Medicine) in Clinical Pharmacology & Therapeutics from Nizam’s Institute of Medical Sciences, MD (Doctor of Medicine) Pharmacology from Mamata Medical College and MBBS from AIMS, Karnataka. Dr. Kiran is also a certified Diabetologist. He is a member of Indian Pharmacological Society (IPS) and Indian Medical Association (IMA).
Mr. Gopi Krishna is Sr. Manager in quality assurance dept. at Jeevan. He is responsible for assuring Bioanalytical studies and Clinical Trials are conducted in accordance with ICH GCP/GLP guidelines, applicable regulations/guidelines and SOPs. Gopi has over 10 years of experience in clinical research quality assurance, with an international exposure in UK and Malaysia. He has worked in QA department of clinical research organization for conducting BA/BE studies, early and late phase trial audits in compliance with applicable GCP/GLP regulations and drug regulatory affairs. He has handled/facilitated various regulatory/client audit proceedings. He also instrumental in setting up QMS for early phase trials and BA/BE trials. Earlier he was associated with DRA QA Compliance Manager at Novartis India, Auditor at Veeda Clinical research UK, Sr. Auditor Veeda Clinical Research India and Research Associate at GVK biosciences India and holds a Master's degree in Pharmacy.