Senior Analyst - Toxicology - Bangalore
Evalueserve · Bengaluru · onsite · Posted 70d ago
Undisclosed3–5 yrsfulltimeSourced from
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About this role
Job Summary
Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
We are seeking an experienced Toxicologist with expertise in OECD guidelines and risk assessment. The ideal candidate will ensure full compliance with GLP, OECD, ICH, IAEC, and institutional standards, actively participate in study plan reviews, protocol amendments, and pathology audits, and support regulatory documentation. Strong attention to detail and knowledge of regulatory frameworks are essential.
Key Responsibilities - Prepare comprehensive Common Technical Document (CTD) dossiers in compliance with international regulations and marketing submission requirements.
- Develop and review reports on Health Based Exposure Limits (HBELs) such as (PDE/ OEL/ ADI) for various chemicals.
- Conduct scientific literature searches to gather, analyze, and compile relevant scientific data from diverse clinical and non-clinical safety, and efficacy databases.
- Evaluate the quality, produce data summaries, and draw conclusions for various toxicological endpoints such as systemic toxicity, genotoxicity, skin/eye irritation, sensitization, carcinogenicity, reproductive toxicity, developmental toxicity, and toxicokinetics, in accordance with guidelines/ guidance established by OECD, ICH, and EPA.
- Draft environmental and ecotoxicity assessments pertaining to chemicals, specifically addressing factors like persistence, bioaccumulation, and toxicity.
- Master's degree in pharmacy, pharmacology or toxicology with 3 to 5 years of experience in relevant field.
- Proficient in drafting and reviewing non-clinical modules of CTD.
- Preparation of HBELs as per regulatory requirements.
- Regular client interactions and understanding the requirements and deliver the project.
- Demonstrated expertise in writing and submitting hazard or safety documentation in compliance with various regulations such as EU, EPA, ICH, or FDA.
- Familiar with a range of toxicology, pharmacology, clinical, and regulatory databases, as well as their search strategies, for the purpose of identifying high-quality data.
- Demonstrates a comprehensive understanding of diverse toxicological studies and their principles in accordance with OECD guidelines.
- Excellent interpersonal skills and effective written and verbal communication abilities.
- Proficient in completing tasks within assigned areas of responsibility with accuracy and timeliness.
- Exhibits attentive and active listening skills.
- Demonstrates strong teamwork skills and logical reasoning.
- Displays the ability to identify proactive approaches to contribute towards the firm's goals and mission.
- Open to challenging existing practices by introducing innovative work methodologies.
Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
Sourced from naukri
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About Evalueserve
Evalueserve
Analytics & KPO
4.2k+
employees
2000
26 years old
Gurgaon / Gurugram, Haryana
India
₹12.7L PA avg
Avg at Evalueserve
About
Evalueserve specializes in technology-enhanced managed services, offering analytics and insights to optimize workflows for financial institutions and enterprises.
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Analytics & KPO
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