Mr. E. Sriram, Senior Manager QA
Mr.E.Sriram is a post graduate in pharmacy practice with around 13 years of experience in quality and regulatory compliance functions. Prior to joining in Quest life sciences he has been associated with reputed CRO like Lotus labs and Par biosciences.
Dr.Kiran, Principal Investigator
Clinical Research Professional with around 6 years of progressive experience in the Healthcare Industry including 4 years in Clinical Trials and 2 years as Medical Officer. Well versed in liaising with healthcare professionals and setting up clinical trials and BA/BE studies.
Mr. Siddhar Selvam, Group Leader - Bioanalytical
Mr. Siddhar Selvam, Group Leader - Bioanalytical is having 5 years of experience in bioanalytical field and has explored method development of challenging vitamins and steroids. He has handled more than 50 method development, validation and sample analysis. He is currently pursuing PhD. He has published various papers in Elsevier journals.
Mr. M. Sirajudeen, Assistant Manager, Pharmacokinetics and Statistics
Mr. M. Sirajudeen is a post graduate in pharmacology with an experience of 6 years in pharmacokinetics, statistics, protocol, report preparations, and experienced in phoenix winnonlin and SAS software. Prior to joining in Quest life sciences he has been associated with reputed CRO’s like Micro Therapeutic research, Semler research centre and Apotex research.
Mr. S. Srinivasan, Manager, Finance and Administration
Mr.S.Srinivasan has joined in Quest Life Sciences P ltd as Head of Accounts & Administration. He has got more than 20 years experience in various Industries in the field of accounts, finance and administration. He is expert in spearheading corporate and financial planning initiatives in Accounts & Finance, Auditing & Taxation, and MIS. Also he has expertise in designing and implementing systems to achieve financial discipline and improve the overall efficiency of the organization. Good relationship management & negotiation skills in liaising with Banks, other financial institutions and various regulatory authorities.
Sarayana.S : Medical Writing.
A pharmaceutical professional with nealry 7 years of experience in Medical and Safety Writing. Worked for CROs and a global pharma company and handled documents like Clinical Study Reports, Synopsis, Protocols Writing, Informed Consent Forms, and Case Report Form, Periodic Safety Update Report, Canadian Annual Summary Report, Case Narratives and Development of Protocol and Results registration in Clinical Trial Registry (ClinicalTrials.gov) for various clinical studies in different therapeutic areas.