Study Director - General Toxicology Aurigene Pharmaceutical Services Limited

5.0 - 9.0 years

0 Lacs

hyderabad, telangana

On-site

The role involves serving as the single point of scientific, administrative, and regulatory control for the study. You will actively participate and supervise all study activities, including animal dosing, clinical signs observation, data collection, and analysis, ensuring compliance with relevant regulations, OECD Principles of GLP, and SOPs. Additionally, you will be responsible for the operation, maintenance, and proper utilization of various equipment/instruments like centrifuges, laminar air flow systems, anesthetic machines, and syringe pumps. Your duties will also include the preparation and updating of SOPs relevant to in vivo and in vitro experiments. Moreover, you will be expected to effectively communicate important information to key study personnel, the sponsor, and other relevant scientists. You will have the authority to approve amendments and deviations to the study plan and must respond to QA findings promptly, ensuring their resolution in a timely manner. As part of this role, you will be responsible for approving study plans, amendments, and reports, as well as ensuring the timely archiving of the study in accordance with existing practices. You will also have all the responsibilities of a Study Director as outlined in the applicable SOPs.,

Posted 6 days ago

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Research Associate/Senior Research Associate - Invivo Pharmacokinetics Enveda Biosciences

3.0 - 5.0 years

4 - 7 Lacs

Hyderabad

Work from Office

You get to collaborate on Work closely with discovery specialists, disease area scientists and in vivo team members. Handling of laboratory animals like rats, mice, Guinea pigs and rabbits. Dose administration to experimental animals by different routes and small animals surgery (like cannulations, CSF fluid collection) and handling, followed by compound dose preparation, administration to experimental animals. Contributing to the ongoing drug discovery programs by conducting in vivo DMPK studies for NCEs with a good knowledge of in vivo animal models. Data generation, analysis, compilation, report preparation. Regular uploading of the data. Conduct statistically supported data (analysis using win online) and deliver results in a timely manner to enable informed decision-making Understanding systems, processes, and compliance. Prepare, review, and deliver scientific presentations for internal/external use. Participate in cross-functional team activities, add value to research projects through creative ideas. Learn from top-notch drug discovery scientists across the world and opportunity to get trained in people skills. PK-PD studies in rats and mice of NCE. Who will thrive in this role? M.Pharm / M.S in Pharmacology with 3-5 years of research experience in either academic or industrial R&D setting. Deep understanding in pharmacokinetics, physiology along with in vivo disease model development and testing. Prior experience in small animal handling, dosing through different routes of administration, dissections and tissue harvesting, tissue processing Fair understanding about the drug discovery process. Excellent organizational, interpersonal, and problem-solving skills Experience of working with different cross functional teams Excellent oral and written communication skills Strong work ethic; scientific curiosity; can-do, will-do attitude. Experience in using electronic lab notebook system

Posted 1 month ago

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