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Location
In office (Mumbai)
Seniority
Junior · 2+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Nov 4, 2026. First seen by Alion on Aug 4, 2026. ClinChoice scores B on the Alion truth index.

Overview
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ClinChoice is a full-service global contract research organization based in Horsham, near Philadelphia, that supports drug, device and consumer health companies through clinical development and post-approval work. Founded in 1995 in Philadelphia, it has more than 3,000 staff across the Americas, Europe, Asia and ANZ offering clinical operations, biometrics, safety, regulatory affairs, medical writing and real-world evidence services, often through functional service placements with sponsors. Openings include statistical programmers, data scientists, clinical research associates, pharmacovigilance scientists, regulatory affairs specialists and business development directors.

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.
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