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3.0 - 7.0 years
0 Lacs
ahmedabad, gujarat
On-site
You will be responsible for driving non-clinical pharmacokinetic studies in various species for animal health products. Your role will involve planning and designing AMES, In vitro and In vivo genotoxicity studies to support impurity qualification in drug substances/products. Additionally, you will provide technical feedback for non-clinical studies, including pharmacokinetic and toxicity studies. Your duties will also include supporting study design and planning for tissue distribution studies, interpreting data, and reviewing study reports in accordance with USFDA, ICH, and OECD guidance for regulatory submissions. You will closely interface with in-house facilities and CROs to ensure the ...
Posted 2 months ago
3.0 - 8.0 years
6 - 16 Lacs
Hyderabad
Work from Office
You Get To Collaborate On The successful candidate will: Plan & execute in vivo pharmacology studies to evaluate the activities of small molecule drug candidates, investigate their mechanisms of action, and explore novel therapeutic hypotheses Contribute to study design, planning and performing in vivo studies related to pharmacokinetic, pharmacodynamic and efficacy studies from early exploratory to IND stage Conduct statistically supported data analysis, and deliver results in a timely manner to enable informed decision-making Record experimental data and observations on a timely basis in company specified format Prepare, review, and deliver scientific presentations for internal/external us...
Posted 3 months ago
11.0 - 16.0 years
12 - 22 Lacs
Bengaluru
Work from Office
Job Title: Section Head (Toxicology)Location: Bangalore Industry: Pre-clinical Contract Research Organization Job Type: Full-time About the Role: We're seeking an experienced Section Head to lead our toxicology team, combining scientific expertise with strategic oversight. This dual-role position demands strong leadership, regulatory knowledge, and cross-functional collaboration to support drug development from discovery to late-stage clinical trials. Key Responsibilities: Design and manage toxicology studies. Mentor teams and shape toxicology strategy across programs. Collaborate with cross-functional teams to support drug development. Requirements: Experience: 12-15 years of relevant exper...
Posted 4 months ago
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