Regulatory Affairs Jobs | IQVIA Is Hiring a Sr Reg Doc Coord | Apply Now
Are you searching for high-paying Regulatory Affairs Jobs in the pharma and clinical research sector? IQVIA Career brings an exciting opportunity for life science graduates to enter the world of regulatory publishing and global submissions. This hybrid role in Bengaluru offers hands-on experience in eCTD publishing, ICH guidelines, and clinical research documentation, making it a strong entry point into life science jobs in the corporate sector.
Job Details
- Job Details: Sr Reg Doc Coord
- Location: Bengaluru, India
- Req ID: R1515567
About the Company
IQVIA is a global leader in clinical research services, commercial insights, and healthcare intelligence. Through IQVIA Career opportunities, professionals contribute to drug development, regulatory submissions, and healthcare innovation worldwide. The company supports pharmaceutical and biotechnology organizations with advanced data analytics and regulatory expertise. IQVIA offers structured growth pathways in regulatory affairs and publishing. This Regulatory Affairs Jobs opportunity is based in Bengaluru in a hybrid working model.
Key Responsibilities
- The Junior Publisher is responsible for supporting the compilation, publishing, and technical quality control of Regulatory submissions
- Supports production of high-quality dossiers by handling the collection of components, publishing / assembly, quality review, and delivery of submissions in paper and electronic format (like NeeS, eCTD, etc.).
- Supports electronic submissions, performs bookmarking, hyper-linking, and tables of content creation according to Health Authority (HA) guidelines.
- Assists with the collection of CSR appendices in accordance with ICH guidelines and IQVIA standard practices, with guidance from the lead medical writer for the CSR
- Interacts with internal clients. May have some external interactions, mostly directed by senior staff
- Takes responsibility for managing day-to-day workload for assigned tasks, in collaboration with senior staff
- Keeps abreast of current data, trends, medical writing/regulatory knowledge, developments and advances in area of drug development/medical writing/regulatory submissions
- Complies with Company SOPs and participates in the implementation of new SOPs
Qualifications
- Bachelor’s degree in a life science-related discipline, preferred understanding of Regulatory Affairs in general, Publishing.
Skills Required
- Knowledge of regulatory submissions
- Strong communication skills
- Attention to detail
- Microsoft Office proficiency
- Time management and multitasking ability
- Willingness to learn and adapt.
If you are aiming to build a long-term career in regulatory affairs within the pharma and clinical research industry, this IQVIA Career opportunity is a strong starting point. These Regulatory Affairs Jobs provide exposure to global submissions and structured corporate growth for life science graduates.
