Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Trainee , Regulatory Affairs

Cencora
Cencora
0-2 years
Not Disclosed
10 Jan. 9, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Trainee – Regulatory Affairs

Location: Noida, India
Job Type: Full-Time
Category: Consulting
Job ID: R2523137


About Cencora

Cencora is a leading healthcare organization committed to creating healthier futures for people and animals worldwide. Our team members are at the core of everything we do, driving innovation and delivering high-impact solutions across human and veterinary health. Join us to make a meaningful difference in the healthcare industry and gain hands-on experience in regulatory affairs.


Position Overview

We are looking for a Trainee in Regulatory Affairs to support our regulatory operations in human and veterinary medicinal products, as well as medical devices, cosmetics, food supplements, and herbal products. This role provides an excellent opportunity to gain practical experience in regulatory processes, document preparation, and compliance while working closely with experienced professionals.


Key Responsibilities

  • Assist in regulatory processes to obtain and maintain marketing authorizations, including applications, renewals, and variations.

  • Support the preparation and compilation of regulatory documents within ongoing projects.

  • Assist in planning and executing client projects in alignment with KPIs and deadlines.

  • Conduct regulatory intelligence to develop and maintain knowledge of relevant regulations and best practices.

  • Collaborate with cross-functional teams to share regulatory insights and contribute to project success.


Required Qualifications & Skills

  • Education: University degree in Life Sciences.

  • Experience: Basic exposure to regulatory affairs or demonstrable capability in a related field. On-the-job learning opportunities will be provided.

  • Skills & Competencies:

    • Strong attention to detail and high service orientation

    • Ability to prioritize and manage tasks efficiently

    • Good written and verbal communication skills

    • Analytical thinking with the ability to identify issues and propose solutions

    • Professional appearance and confident demeanor

  • Language: Business-fluent English


What Cencora Offers

  • Exposure to regulatory affairs across diverse product types including human and veterinary medicines

  • Structured training and mentorship from experienced regulatory professionals

  • Competitive benefits aligned with local market practices

Equal Opportunity Employer: Cencora provides equal employment opportunities without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other protected class. We are committed to providing reasonable accommodations to applicants with disabilities.


Apply Today: Join Cencora to build a strong foundation in regulatory affairs and contribute to innovative healthcare solutions.