Parexel Job Openings: Junior Regulatory Affairs Associate (Remote, Bangalore)
Parexel, a global Clinical Research Organization (CRO), is hiring for the role of Junior Regulatory Affairs Associate. This opportunity is ideal for B.Pharm and M.Pharm graduates with 0–2 years of experience who want to build a career in Regulatory Affairs.
The position is based in Bangalore with a remote working option, making it suitable for freshers and early‑career professionals. In this role, you will support regulatory documentation, submissions, and compliance activities, working with global teams in a structured and learning‑focused environment.
This is a strong entry‑level opportunity for candidates looking to grow in Regulatory Affairs within a global CRO and gain exposure to international regulatory processes.
🏢 About the Company
Parexel is a globally recognized organization that supports pharmaceutical, biotechnology, and medical device companies through clinical research, regulatory strategy, and compliance services. The company operates in multiple countries and follows strict regulatory and quality standards. Working at Parexel allows professionals to gain exposure to international regulatory frameworks and structured project environments that support long‑term career development.
📊 Job Overview
- Position: Junior Regulatory Affairs associate
- Department: Regulatory affairs
- Location: Bangalore(Remote),India
- Experience: 0 to 2 years
- Qualification: B.Pharm, M.pharm
- Job Type: Full-Time
- Last Date of application: Not provided
📋 Key Responsibilities – Junior Regulatory Affairs Associate at Parexel
- Under supervision, provide basic paper and electronic publishing services, including document preparation, legacy document conversion, scanning, rendering, bookmarking, and hyperlinking.
- Assist in compiling regulatory submissions, including table of contents creation, pagination, volumization, and formatting of reports and simple regulatory submissions.
- Support preparation of regulatory submission packages in accordance with global regulatory requirements.
- Ensure published documents meet quality, accuracy, and formatting standards before submission.
- identify opportunities to improve project efficiency, turnaround times, or documentation quality.
🎓 Eligibility Criteria
- The ideal candidate will have 0 to 2 years of experience working in an industry‑related environment, preferably within pharmaceutical, life sciences, regulatory, or clinical research settings. This role is well‑suited for fresh graduates who are eager to begin their careers and gain hands‑on exposure in a professional regulatory environment.
- A Bachelor’s degree in a scientific or technical discipline is required for this role. Candidates with an academic background in pharmacy, life sciences, biotechnology, chemistry, or related fields are strongly encouraged to apply.
- Demonstrates the ability to work effectively within a team environment, contributing positively to shared goals and deliverables.
- Performs assigned tasks within broad project guidelines, under the direction of a Project Technical Lead or Project Manager.
- With appropriate guidance, shows the ability to prioritize tasks and manage time efficiently to achieve defined project outcomes and deadlines.
- Actively seeks opportunities to improve individual performance, welcomes feedback, and applies learnings shared by project leads and colleagues.
- Uses instructions, training, and information provided by senior team members to successfully complete assigned project activities.
- Consistently delivers high‑quality work that meets the expectations of both the Project Lead and the client
⭐ Job Role Insight
The Junior Regulatory Affairs Associate role is an entry‑level position that helps professionals understand how regulatory compliance supports product development and approvals. By working on documentation and submission support tasks, candidates gain insight into how regulatory activities impact the lifecycle of pharmaceutical products. This role builds a strong foundation for advanced regulatory positions.
🎯 Who Should Apply
- This opportunity is suitable for:
- Individuals with documentation or compliance exposure
- Fresh graduates interested in Regulatory Affairs
- Candidates seeking entry‑level RA roles
- Professionals transitioning into regulatory functions
💰 Salary & Work Model Insight
- Salary Range: As per company standards
- Work Mode: Remote (with structured work schedules)
- Compensation depends on experience, skill set, and internal policies.
💡 Preparation Tips
- Revise basic regulatory terminology and concepts
- Learn how regulatory documentation is structured
- Highlight attention‑to‑detail skills in your resume
- Be prepared to explain your interest in regulatory affairs
🔗 Application Process
Interested candidates should apply only through the official company career website using the link provided below.
Important Disclaimer
This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official website before applying.
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FAQ – Junior Regulatory Affairs Associate
1. Who is eligible to apply for this role?
This role is suitable for candidates with 0 to 2 years of experience in an industry‑related environment. Fresh graduates with a relevant scientific or technical background are encouraged to apply, provided they are eager to learn and grow in a regulatory or life sciences setting.
2. What educational background is required for this position?
Applicants must have a Bachelor’s degree in a scientific or technical discipline. Degrees in pharmacy, life sciences, biotechnology, chemistry, or related fields are highly preferred.
3. Is this role suitable for freshers?
Yes. This is an entry‑level position designed for fresh graduates or early‑career professionals. The role offers structured guidance, supervision, and learning opportunities to help candidates develop practical industry skills.
4. What type of work environment can candidates expect?
Candidates will work in a collaborative, team‑oriented environment under the guidance of a Project Technical Lead or Project Manager. The role emphasizes communication, teamwork, and adherence to defined project guidelines.
5. Will training or guidance be provided?
Yes. Candidates will receive ongoing guidance and support from project leads and senior colleagues. Learning is encouraged through feedback, practical exposure, and application of knowledge provided by experienced team members.
