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Rajashekhar is seeking a position utilizing his 1 year of experience in clinical operations and clinical trial management systems. He has skills in clinical data management, maintaining study documents and reports, and a thorough understanding of ICH GCP guidelines and pharmacovigilance. He has a B.Pharmacy from JNTU Hyderabad and completed an industrial training in healthcare.
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Narendra Konduri is seeking a career opportunity in clinical research, pharmacovigilance, or data management. He has over 2 years of experience and holds a diploma in these fields from NOMAD Life Sciences Pvt. Ltd. He also has a B.Pharmacy degree from Shri Vishnu College of Pharmacy. Narendra has good knowledge of ICH GCP guidelines, clinical trials, pharmacovigilance, MedDRA, and data management software like Oracle Clinical and OpenClinica. He has experience with tasks like SAE reporting, case report form review, and data validation. Narendra declares that he will put his best efforts to work productively if given anJeyasree New 29.12.2016
Jeyasree New 29.12.2016Jeya sree
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Jeyasree Prabinraj is an experienced Indian pharmacist seeking a pharmacist position. She has over 5 years of experience working in production and hospital pharmacy settings in India. She has a Bachelor of Pharmacy degree and diploma in pharmacy. Her skills include dispensing medications, maintaining documentation, customer service, and training staff. She is looking to apply her skills and experience in a modern pharmacy.SRAVAN RESUME
SRAVAN RESUMESravan Kumar
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This curriculum vitae is for Sravan Akumalla, who has 1 year of experience as a clinical data analyst. He is proficient in Oracle Clinical Database and has experience using Conduct Phase. He has a strong understanding of clinical trial processes, ICH-GCP guidelines, CDISC standards, and FDA regulations. Currently employed as a clinical data analyst by Phase Clinica Life Sciences, his responsibilities include data management, data entry, query tracking, and ensuring data quality.ARJUN_M.Pharm_Pharmaceutics PV
ARJUN_M.Pharm_Pharmaceutics PVArjun Sagar
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This document contains the resume of Arjun Avula. It summarizes his educational qualifications, skills, work experience, and objective. He has an M.Pharmacy from TKR College of Pharmacy with 74% and a B.Pharmacy from SLC's College of Pharmacy with 70.1%. He has work experience in pharmacovigilance and has hands-on experience using Oracle Argus Safety software. His skills include handling laboratory instruments and knowledge of formulation processes. He aims to work in a pharmaceutical research organization where he can contribute to career and organizational growth.ROSHAN CV (2) (1) (1)
ROSHAN CV (2) (1) (1)ROSHANKUMAR shetty
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Roshan Kumar S is a Clinical Process Associate-2 with 1.8 years of experience in clinical research. He has thorough knowledge of clinical trials, ICH-GCP guidelines, and medical terminology. His roles include performing administrative tasks, assisting with data management, establishing communications, and ensuring documentation quality. He also monitors studies and communicates with clients, and has skills in computer programs, analytics, communication, and time management.Resume-SonaliP_ regulatory writing 1
Resume-SonaliP_ regulatory writing 1sonali parmar
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Sonali Parmar has over 11 years of experience in regulatory writing, medical writing, and project management. She has expertise in writing regulatory documents like CMCs and CTDs for US and EU markets. She is proficient in writing clinical study reports, literature reviews, and regulatory documents. Currently she works as a validation consultant for a top pharmaceutical company, providing regulatory and medical writing deliverables.CV _Suresh Revanna_2016
CV _Suresh Revanna_2016Suresh Revanna
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Suresh Revanna has over 16 years of experience in the pharmaceutical industry, specializing in analytical development, quality assurance, and regulatory compliance. He currently works as a Principal Scientist at Novartis Healthcare Pvt Ltd in Hyderabad, India. Prior to this, he held roles at Emcure Pharmaceuticals Ltd, Brown & Burk Pharmaceuticals Ltd, and Sanford Analytical Labs. Suresh has a B.Sc. in Chemistry, M.Sc. in Environmental Chemistry, and a diploma in Intellectual Property Rights. At Novartis, his responsibilities include method development and validation, stability studies, authoring regulatory documents, and managing the quality and compliance team.M Kashaan_01 Oct 2016
M Kashaan_01 Oct 2016Dr M.Kashaan Siddiqui
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Dr. Mohammad Kashaan has over 4 years of experience in pharmacovigilance, regulatory affairs, and clinical research. He holds a Bachelor's in Dental Surgery and a Master's in Clinical Research. His skills include processing adverse event reports, database management, and ensuring compliance with regulatory guidelines. Currently he works as an Independent Quality Reviewer at Cognizant Technology Solutions, where he leads a team of 30 associates and publishes monthly quality reports.HR Assistant.
HR Assistant.mahesh kumar Sharma
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Mahesh Kumar Sharma is applying for an HR Assistant position. He has over 10 years of experience in HR roles, most recently as an HR Assistant Manager at Camberwel Diagnostics Pvt Ltd from 2009 to 2012. He has a bachelor's degree in science, a diploma in medical lab technology, an MBA, and certificates in computer skills. His objective is to establish himself in a managerial role where he can integrate his vision of success with teamwork.Resume (4)
- 1. CURRICULUM VITAE Name: Rajashekhar Email: rajashekerregunta@gmail.com Mobile : +91 9014243483 Objective: Seeking a position where my skills and abilities could be utilized for professional growth that would expand my horizons while being resourceful, innovative and flexible, take on the challenges in a responsible way with discipline and willingness for the hard work. Professional Summary Had around 1year experience as clinical process trainee in clinical operations. Hands of experience on CTMS (Clinical trial management systems) and Edcs like INFORM, IWRS, MEDIDATAetc. Handling Creating subjects, status changes, subject visit tracking, triggering payments, CRF tracking Maintaining minutes of meeting, preparing and distributing status reports, creating and maintaining study documents, Assist in updating and maintaining systems within project timelines and per project plans Have good knowledge on Clinical data management(Study and Conduct phase, CRF annotation, Discrepancy management) Good understanding of ICH GCP Guidelines Thorough knowledge of pharmacovigilance Complete understanding of reference safety information and case processing. Professional Experience Working as a Clinical Process Trainee in Quintiles Ltd. from Sep 2015 to till date. Educational Qualification B.Pharmacy from JNTU Hyderabad. Industrial Skills: Have obtained industrial training for one month in S. S .HEALTH CARE. Where i have obtained an exposure to industries and equipment used.
- 2. Academic Project: Project title : Method development and validation of Imatinib by RP HPLC method. Position : Team leader. Guidance : Dr.U.Praveen Kumar Description : According to the literature survey it was found that few analytical Methods such as (HPLC, UV-Visible analysis and LC-MS) were reported for the estimation of Imatinib. The objective of the proposed method is to develop simple and accurate methods for the determination of Imatinib by RP-HPLC method in pharmaceutical dosage forms & its stability indicative studies. Strengths Hardworking nature with a positive attitude. Being stable even in contradicting situations. Like to take responsibilities and challenges. Personal Profile: Name : R. Rajashekhar Fathers Name : R.Lingam Date Of Birth : 10-03-1992 Marital Status : Single Languages Known : Telugu, Hindi and English Declaration: I hereby declare that the above information is true to my knowledge .I would prove myself and would serve my level best for growth of organization. Date: Place: (R.RAJASHEKHAR)