
Mahesh Avula
Avula Mahesh 2-10, Yadavali, Maddikera,Kurnool, Andhra Pradesh-518385. 9642749831 [email protected] I am seeking for Clinical research associate/ Clinical data management/ Clinical SAS/Pharmacovigilance... | Kurnool, Andhra Pradesh, India
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Mahesh Avula’s Emails ma****@qp****.com
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Mahesh Avula’s Location Kurnool, Andhra Pradesh, India
Mahesh Avula’s Expertise Avula Mahesh 2-10, Yadavali, Maddikera,Kurnool, Andhra Pradesh-518385. 9642749831 [email protected] I am seeking for Clinical research associate/ Clinical data management/ Clinical SAS/Pharmacovigilance positions. I have completed Master of Pharmacy in department of Pharmacology (M.pharm) from ANCP-JNTUA University. I have been an active member of the academic project [In Vitro Pharmacological Evaluation of Ethanolic Extract of Cryptolepis buchanani Roem & Schult Leaves on Colorectal cancer, Hepatocellular carcinoma, Spasmodic and Ulcer activities and Validation methods of Dapsone drug with comparative study of standard and sample by using UV-SPECTEOCTROSCOPY.] & have got a practical knowledge during this project tenure. My core areas are Preclinical studies, Clinical trials and research, Basic knowledge in Docking software (BIOVIA) handling, Microsoft Office and Internet Applications. I am currently working in CRO(clinical Research) as a Clinical Research Executive (Clinical Research Coordinator) in QPS Bioserve Indian Pvt Ltd, Hyderabad. As per my job I handle: *Conduct and ensure the studies incompliance with GCP. *Documentation of trail data (CRF's) *Clinical data review and Data management. * Ensure Adverse Events are reported appropriately, accurately and in a timely manner and that follow-up *Entry and maintain list of AEs in the CDMS study wise *Coordinating with all study personnel and ensures completion of all trial activities in timely manner with accordance to protocol and SOP. *Manage trial master file contents and ensure the implementation of project plans as assigned. *Provide support and timely follow-up for all audit and quality assurance activities. Skills: Clinical Trials and Research Clinical data documentation (CRF's) Clinical data review Knowledge on ICH-GCP Guidelines Knowledge in Clinical data management Knowledge in Medidata Rave Knowledge in Clinical SAS Knowledge in pharmacovigilance Knowledge in BA/BE clinical research studies Microsoft office and Internet Sincerely, Avula Mahesh Ph: 9642749831 Mail: [email protected]
Mahesh Avula’s Current Industry Qps Bioserve
Mahesh
Avula’s Prior Industry
Csir
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Qps Bioserve
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Work Experience

Qps Bioserve
Clinical Research Executive
Wed Mar 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Present
Csir
Summer Research Intern
Fri May 01 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Dec 01 2020 00:00:00 GMT+0000 (Coordinated Universal Time)