5.0 - 10.0 years

4 - 9 Lacs

hyderabad

Work from Office

Preparation of study plan considering the client requirements as well as regulatory requirements. Preparing a study schedule and communicating with all the study personnel and ensuring the proper conduct of the study. Preparing reports after completion of each study. This involves evaluating the data output by applying scientific knowledge and skills. To maintain the highest regulatory standards (OECD GLP) during any activity conducted in the facility by continuous monitoring and checkup of all the instruments/equipment used in a study as per Standard Operating Procedures (SOPs). Preparation and periodic revision of Standard Operating Procedures. Preparation and presentation of experiment conduct protocols to the Institutional Animal Ethics committee. Periodically verify data generated during study. Archival of the study plan, study report, raw data and related materials as per the study plan. Coordinate with TFM and/or study personnel and keeping informed of their findings during the study and receipt and evaluation of their respective individual reports for inclusion in the final study report.

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Invitro DMPK Scientist AVE-Promagne Business Solutions

2.0 - 7.0 years

10 - 11 Lacs

Hyderabad

Work from Office

Your key responsibilities will include conducting In Vitro ADME studies This involves reading and understanding various in vitro ADME protocols, as well as performing in vitro stability experiments for new chemical entities in liver microsomes, plasma, and other relevant matrices You will also conduct specific in vitro ADME experiments such as logP, logD, pKa measurements, CYP induction and inhibition assays, permeability determinations, CYP phenotyping, and solubility determinations in various cell lines In addition to in vitro ADME studies, you will be involved in bioanalysis activities This includes developing and validating LC-MS/MS and HPLC-UV/PDA methods, conducting bioanalytical QC, and handling bioanalytical method development for various matrices with a focus on in vitro samples Experience in developing LC-MS/MS methods for biochemical and cell-based screening of NCEs is a plus You will also be responsible for general LC-MS/MS and HPLC maintenance and troubleshooting tasks Furthermore, as part of your role, you will be required to analyze data, generate reports, and share them with the line manager This involves understanding the quality of bioanalytical data, conducting data analysis using software like Phoenix WinNonLin, calculating in vitro results/parameters using Excel spreadsheets, and generating reports in Excel, Word, and PowerPoint formats You will also be responsible for generating reports in both GLP and non-GLP formats based on the requirements

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Invitro Research Scientist AVE-Promagne Business Solutions

2.0 - 7.0 years

10 - 11 Lacs

Hyderabad

Work from Office

Your key responsibilities will include conducting In Vitro ADME studies. This involves reading and understanding various in vitro ADME protocols, as well as performing in vitro stability experiments for new chemical entities in liver microsomes, plasma, and other relevant matrices. You will also conduct specific in vitro ADME experiments such as logP, logD, pKa measurements, CYP induction and inhibition assays, permeability determinations, CYP phenotyping, and solubility determinations in various cell lines. In addition to in vitro ADME studies, you will be involved in bioanalysis activities. This includes developing and validating LC-MS/MS and HPLC-UV/PDA methods, conducting bioanalytical QC, and handling bioanalytical method development for various matrices with a focus on in vitro samples. Experience in developing LC-MS/MS methods for biochemical and cell-based screening of NCEs is a plus. You will also be responsible for general LC-MS/MS and HPLC maintenance and troubleshooting tasks. Furthermore, as part of your role, you will be required to analyze data, generate reports, and share them with the line manager. This involves understanding the quality of bioanalytical data, conducting data analysis using software like Phoenix WinNonLin, calculating in vitro results/parameters using Excel spreadsheets, and generating reports in Excel, Word, and PowerPoint formats. You will also be responsible for generating reports in both GLP and non-GLP formats based on the requirements.

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DGM Invitro Biology Eminence Hr Services Bharuch

10.0 - 20.0 years

27 - 42 Lacs

Vadodara

Work from Office

Familiarity with multiple and diverse bioassay techniques for study of enzymes, kinases, GPCR’s, RNA binding proteins, epigenetic targets etc. Required Candidate profile Oversee in vitro screening experiments and generate reports in a timely manner Propose new ideas, conduct and assist in target evaluations & due diligences

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Business Development Executive For a Diagnostic CO Eugenics Management Services (p) Ltd.

2.0 - 4.0 years

4 - 5 Lacs

Guwahati

Work from Office

Marketing mapping Understand client needs & develop revenue pipeline in alignment with the BD strategy Identifying new biz opportunities & capitalize Negotiate & close contracts/agreements as per policy Farming existing clients & ensuring growth Required Candidate profile Manage & develop customer relationship & customer satisfaction Client retention Responsible for cross dept. collaboration across Co for smooth operations Responsible for sales for the assigned area

Posted 3 months ago

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