Job Description
Job Title: Associate – Regulatory Toxicology
Employment Type: Full-time
Location: Mumbai, India
About ClinChoice
ClinChoice is a partner to the largest pharmaceutical, medical device, and consumer care innovators in the world. Established in 1995, we provide expertise in clinical operations, biometrics, regulatory affairs, pharmacovigilance, medical affairs, and toxicology to help our partners advance healthcare by accelerating clinical trials with data-driven insights, delivering the best strategies for product registration, and enhancing patient safety through real-world and clinical analysis.
Our global delivery network has expanded to centers and satellite offices in the United States, Mexico, the United Kingdom, Armenia, China, Japan, India, and the Philippines to help our customers maintain regulatory compliance locally and globally.
We have forged future-defining partnerships with industry bodies and technology companies to develop cutting-edge solutions that deliver our expertise with quality and precision.
Primary Responsibilities:
• Conduct literature searches and prepare toxicological assessments of various raw materials/ingredients used in consumer and OTC products.
• Create Raw Material Toxicology Profiles for INCI ingredients as well as residual chemicals.
• Conduct risk assessments for raw materials used in cosmetic applications, including Margin of Safety and California Proposition 65 calculations.
• Draft Full Safety Assessments as required by the European Cosmetics Directive.
• Draft safety assessments for impurities and degradants based on requirements.
• Draft Full Safety Assessments, including recommendations for the approval of formulas.
• Complete all assigned training within the specified timelines.
• Participate in Process Improvement Initiatives to maintain the Quality and Compliance score.
• Escalate any issues encountered during daily activities to the Team Lead on a daily basis.
Candidate Profile:
• Minimum of 2–4 years of experience in the pharmaceutical industry as a Regulatory Toxicologist.
• Master's degree in Toxicology or Veterinary Pharmacology.
• Good verbal and written communication and presentation skills in English.
• Should be proactive and initiative-driven.
• Should be solution-centric in approach.
Skills Required
- 2-4 years experience in the pharmaceutical industry as a Regulatory Toxicologist
- Master's degree in Toxicology or Veterinary Pharmacology
- Ability to conduct literature searches and prepare toxicological and safety assessments
- Knowledge of INCI ingredients, residual chemicals, and cosmetic safety assessment practices
- Ability to perform risk assessments including Margin of Safety and California Proposition 65 calculations
- Good verbal and written communication and presentation skills in English
- Proactive, initiative-driven and solution-centric approach
ClinChoice Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about ClinChoice and has not been reviewed or approved by ClinChoice.
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Flexible Benefits — Flexible arrangements, including telecommuting and flextime with no core hours in some regions, are highlighted for many roles. Feedback suggests flexibility is commonly available but depends on role and location.
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Leave & Time Off Breadth — Vacation, personal, and sick days are part of the core package, with some markets granting paid leave from the date of hire. Feedback suggests time off is standard-to-decent across locations, though specifics vary.
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Healthcare Strength — Health coverage is positioned as a core benefit, with some accounts describing overall benefits as full or good. In the U.S., healthcare sits within a conventional CRO package alongside medical, dental, and vision.
ClinChoice Insights
What We Do
ClinChoice is a global full-service Contract Research Organization (CRO) specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies, aiming to accelerate the development and commercialization of innovative drugs and devices.
