Parexel is hiring a Junior Regulatory Affairs Associate for its Bengaluru (Remote) location. This entry-level regulatory affairs job at Parexel is designed for candidates looking to build a career in clinical research, regulatory submissions, and document management within the global pharmaceutical and life sciences industry.
The Junior Regulatory Affairs Associate role at Parexel focuses on supporting regulatory publishing activities, document control, and submission preparation under supervision. It is an excellent opportunity for fresh graduates or early professionals (0โ2 years experience) seeking growth in regulatory operations and clinical development services.
Key Responsibilities โ Junior Regulatory Affairs Associate
As a Junior Regulatory Affairs Associate at Parexel, your responsibilities include:
- Supporting basic regulatory affairs submissions and document publishing activities
- Preparing submission packages under supervision
- Performing document formatting, pagination, bookmarking, hyperlinking, and table of contents creation
- Assisting in scanning, conversion, and archival of regulatory documents
- Managing file transfer, storage, and tracking of regulatory guidelines
- Supporting document management systems and submission lifecycle tasks
- Ensuring compliance with global regulatory submission standards
- Collaborating with project teams to improve efficiency and deliverables
- Following SOPs and internal regulatory procedures
Required Qualifications
To apply for this Junior Regulatory Affairs Associate job at Parexel, candidates must have:
- Bachelorโs degree in a scientific or technical discipline
- 0โ2 years of experience in pharmaceutical, clinical research, or regulatory affairs
- Basic understanding of regulatory documentation and submission processes
- Familiarity with document management tools is an advantage
- Strong attention to detail and organizational skills
- Ability to work in a team-based, supervised environment
Skills Required
- Regulatory document publishing & formatting
- Project execution and coordination
- Basic regulatory compliance knowledge
- Communication and teamwork skills
- Time management and task prioritization
- Adaptability in a clinical research environment
Benefits of Working at Parexel
- Opportunity to work with a global clinical research organization
- Exposure to international regulatory standards
- Structured learning in regulatory affairs and submissions
- Remote working flexibility (Bengaluru-based role)
- Career growth in pharmaceutical and clinical development domain
- Supportive and inclusive work environment
How to Apply
