Apply for Junior Regulatory Affairs Associate job at Parexel Bengaluru remote. Check eligibility, responsibilities, salary, and application process today online.
Introduction
The Junior Regulatory Affairs Associate Job at Parexel is an excellent opportunity for freshers and early-career professionals aiming to enter the regulatory affairs domain. This role provides hands-on experience in global regulatory submissions, document management, and clinical development support. If you have a scientific background and want to build a long-term career in pharma or clinical research, this position can be a strong starting point.
Job Overview
| Job Details | Information |
|---|---|
| Job Title | Junior Regulatory Affairs Associate |
| Company Name | Parexel |
| Location | Bengaluru, India (Remote) |
| Employment Type | Full-Time |
| Department | Regulatory Affairs |
| Experience Required | 0–2 Years |
| Education | Bachelor’s Degree (Scientific/Technical) |
| Salary | As per company norms |
Company Overview
Parexel is a leading global Clinical Research Organization (CRO) that supports pharmaceutical and biotechnology companies in developing life-saving therapies. With a strong presence worldwide, the company offers services across clinical trials, regulatory consulting, and market access. Parexel is known for its patient-centric approach, high-quality standards, and innovation-driven culture.
Job Location & Employment Type
- Location: Bengaluru (Remote Opportunity)
- Employment Type: Full-Time
- Work Mode: Work-from-home flexibility with global team collaboration
Open Positions / Department Details
This role is part of the Regulatory Affairs team, where candidates will assist in preparing and managing regulatory submissions, documentation, and compliance-related tasks. It is an entry-level role designed to help candidates understand global regulatory frameworks and submission standards.
Key Roles & Responsibilities
The Junior Regulatory Affairs Associate Job at Parexel involves a variety of entry-level regulatory and documentation tasks, including:
Project Administration
- Assisting in preparing regulatory documents and submission packages
- Performing publishing tasks such as formatting, pagination, and compiling reports
- Supporting document conversion, scanning, bookmarking, and hyperlinking
- Creating structured documents including tables of contents and submission-ready files
- Contributing to improving team productivity and project efficiency
Document Management
- Handling file storage, tracking, and archival of regulatory documents
- Managing electronic document systems and ensuring proper organization
- Supporting compliance with global regulatory submission standards
Standard Operating Procedures (SOPs)
- Learning and following internal SOPs and work instructions
- Ensuring tasks are completed according to regulatory guidelines
Product Support
- Assisting in regulatory support for marketed products
- Providing documentation and compliance-related assistance under supervision
Eligibility Criteria
Education
- Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or any scientific/technical discipline
Experience
- 0–2 years of experience in regulatory affairs or related industry
- Freshers with relevant knowledge can also apply
Skills Required
- Basic understanding of regulatory affairs and submission processes
- Strong attention to detail and document handling skills
- Ability to work in a team environment
- Good communication and coordination skills
- Time management and task prioritization abilities
- Familiarity with MS Office tools (Word, Excel, PowerPoint)
- Willingness to learn global regulatory guidelines
Salary & Benefits
- Salary: As per company norms
- Additional benefits may include:
- Work-from-home flexibility
- Health and wellness benefits
- Learning and training programs
- Career growth opportunities in regulatory affairs
- Exposure to international regulatory standards
Selection Process
The hiring process typically includes:
- Resume shortlisting
- HR interview
- Technical interview
- Final selection and offer
How to Apply
Candidates interested in the Junior Regulatory Affairs Associate Job at Parexel can apply through the official online application portal. Ensure your resume highlights relevant academic background and any regulatory or documentation experience.
Important Dates
- Application Deadline: Apply as early as possible
Why Apply for This Job?
Here are some strong reasons to consider this opportunity:
- Ideal entry-level role in Regulatory Affairs
- Opportunity to work with a globally recognized CRO
- Gain exposure to international submission standards and processes
- Work remotely with global teams
- Develop core skills in documentation, compliance, and project coordination
- Strong career growth path in pharma, biotech, and clinical research industries
This role is perfect for candidates who want to build expertise in regulatory operations and work on global pharmaceutical projects.
FAQs
1. Who can apply for the Junior Regulatory Affairs Associate role?
Candidates with a Bachelor’s degree in a scientific or technical field and 0–2 years of experience can apply.
2. Is this a remote job?
Yes, this position is based in Bengaluru but offers remote working flexibility.
3. What skills are important for this role?
Key skills include documentation handling, communication, attention to detail, and basic regulatory knowledge.
4. What is the salary offered?
The salary is provided as per company norms and depends on candidate experience.
5. Is this job suitable for freshers?
Yes, freshers with relevant educational background and interest in regulatory affairs can apply.
Conclusion
The Junior Regulatory Affairs Associate Job at Parexel 2026 is a great opportunity for fresh graduates and early professionals to step into the regulatory domain. With global exposure, structured training, and a supportive work environment, this role can help you build a successful career in the pharmaceutical and clinical research industry. Apply now to kickstart your journey.
Disclaimer
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