Regulatory Affairs Job at ClinChoice | Life Sciences | Freshers | Apply Now
ClinChoice is seeking a detail-oriented Associate – Regulatory Affairs (Publishing) to join its office-based team in Chennai. This contract-based Regulatory Affairs Job is an excellent entry point for graduates looking for a high-impact Life Sciences Job that focuses on the digital side of pharmaceutical compliance. As an Associate, you will play a vital role in ensuring that clinical and product data are formatted, validated, and submitted to global health authorities with absolute precision.
- Job Title: Associate – Regulatory Affairs (Publishing)
- Location: Chennai, India
About the Company
ClinChoice is a premier global partner to the world’s largest pharmaceutical, medical device, and consumer care innovators. Established in 1995, the company provides expert services across clinical operations, biometrics, regulatory affairs, and pharmacovigilance to accelerate clinical trials and enhance patient safety. With a robust global delivery network spanning the United States, Europe, and Asia, ClinChoice helps customers maintain regulatory compliance both locally and globally. For those pursuing a career in Regulatory Affairs Job opportunities or in regulatory science, ClinChoice offers a collaborative environment where data-driven insights and cutting-edge technology—such as Veeva Vault and Lorenz DocuBridge—are used to advance global healthcare.
Key Responsibilities
In this role, you will be responsible for the technical preparation and lifecycle management of regulatory sequences, which are core tasks for any career in Regulatory Affairs Job positions.
- Submission Support: Support the preparation of electronic Common Technical Document (eCTD) and non-eCTD submissions.
- Document Optimization: Perform critical document formatting, hyperlinking, bookmarking, and PDF optimization to meet agency standards—a necessity for anyone aiming to excel in a Regulatory Affairs Job.
- Compilation & Validation: Assist in submission compilation and conduct rigorous technical validation checks prior to final submission, reflecting key skills required.
- Lifecycle Management: Support ongoing lifecycle activities, including the management of “new,” “replace,” and “delete” sequences, which is a fundamental aspect in Regulatory Affairs profiles.
- Data Integrity: Maintain accurate submission trackers, documentation logs, and ensure metadata accuracy for all document placements—tasks that are highly relevant for Regulatory Affairs candidates.
Qulaifications & Experience
ClinChoice is looking for motivated individuals with a strong scientific foundation and a willingness to master publishing tools, qualities valued in Regulatory Affairs Job applicants.
- Education: A Bachelor’s degree in Life Sciences or Biotechnology is preferred for Regulatory Affairs Job roles.
- Experience: 0–1 year of experience (freshers are encouraged to apply).
- Technical Skills:
- Proficiency in MS Office (Word, Excel, PowerPoint) is a key skill in Regulatory Affairs Job postings.
- Exposure to eCTD publishing concepts and familiarity with tools like Lorenz DocuBridge or Veeva Vault is an advantage for Regulatory Affairs Job seekers.
- Core Competencies:
- High attention to detail and strong time management skills will set you apart in Regulatory Affairs roles.
- Good written and verbal communication skills for team collaboration are always prized opportunities.
- A proactive willingness to learn the regulatory environment and submission lifecycles is essential for those pursuing a Regulatory Affairs Job.
Choosing a Regulatory Affairs Job at ClinChoice is a strategic move for any graduate seeking a specialized Life Sciences Job in Chennai. This role provides the technical training and global exposure necessary to become an expert in eCTD publishing—a critical niche in the Biotechnology Job market. If you are a fresher with a degree in Pharmacy or Biotech and have a keen eye for detail, your career in regulatory publishing starts here. Ensure your application highlights your familiarity with document formatting and your eagerness to work with industry-standard publishing software.
