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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 completion of allocated projects within stipulated cost and timelines. To excel in this role, you should be well-versed in global guidance such as ICH, OECD, and other regulatory requirements. Excellent communication skills and the ability to work effectively in a team are essential for success in this position.,
Posted 1 month 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 use Communicate the status of projects, challenges and results to stakeholdersParticipate in cross-functional team activities, add value to research projects through creative ideas. Who will thrive in this role M.Pharm. with 8-9 years or PhD with 3-5 years of experience in drug discovery industry First hand experience with in vivo animal models and ex vivo biomarkers analysis. Self-motivated, proactive, and able to work independentlyExcellent oral and written communication skills Strong work ethic; scientific curiosity; can do, will do attitude Experience in using electronic lab notebook system If you don't meet all of the requirements listed here, we still encourage you to apply. No job description is perfect, and we might find an even more suitable opportunity that matches your experience.
Posted 2 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 experience in toxicology or a related field. Education: Ph.D. or Master's degree in Veterinary Sciences or Biosciences. Desirable Certifications: DABT Certification and FELASA certification. Skills: Expertise in acute and repeat-dose toxicity studies. Strong understanding of pharmaceutical R&D and agrochemical testing processes. Proven cross-functional team collaboration. In-depth knowledge of GLP and global regulatory guidelines. Excellent scientific writing and communication skills. Strong team leadership and project management skills. High proficiency in data analysis and interpretation. Behavioral Competencies: Excellent communication and adaptability. Effective time management. Proven mentoring and team leadership. Experience integrating toxicology insights into clinical development. Ability to manage complex studies and cross-functional teams. What We Offer: Opportunity to lead in a dynamic CRO environment. Collaborative team. Growth opportunities. If you're a seasoned professional with expertise in toxicology and leadership, apply now with your resume. How to Apply: Email: Sekhar.Sompalli@advinus.eurofinsasia.com We look forward to hearing from you!
Posted 2 months ago
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