IQVIA Hiring for Regulatory Affairs Officer in Bangalore. Explore responsibilities, qualifications, and online application process here.
IQVIA Regulatory Affairs Officer Recruitment 2025
IQVIA, a global leader in healthcare intelligence and clinical research services, is inviting qualified candidates to apply for the position of Regulatory Affairs Officer based in Bangalore, India. This is a full-time opportunity for professionals who are passionate about supporting global clinical development and regulatory operations. IQVIA Hiring for Regulatory Affairs Officer
The Regulatory Affairs Officer will be responsible for preparing and reviewing regulatory submissions and documentation to support clinical trial activities and marketing authorization efforts. This position plays a vital role in ensuring compliance with regulatory requirements and supporting clients across the life sciences and healthcare sectors. IQVIA Hiring for Regulatory Affairs Officer
If you are seeking a challenging and rewarding role in a global organization committed to innovation, collaboration, and improving patient outcomes, this opportunity at IQVIA could be the next big step in your career. IQVIA Hiring for Regulatory Affairs Officer
About IQVIA
IQVIA is a world-renowned organization providing advanced analytics, technology solutions, and clinical research services to the life sciences industry. The company is known for creating intelligent connections that accelerate the development and commercialization of innovative medical treatments. IQVIA Hiring for Regulatory Affairs Officer
With operations in over 100 countries and a strong global team, IQVIA helps clients improve healthcare delivery, enhance patient outcomes, and drive innovation across the pharmaceutical and biotechnology industries. By combining data, technology, and deep scientific expertise, IQVIA continues to play a critical role in transforming how healthcare decisions are made and therapies are delivered. IQVIA Hiring for Regulatory Affairs Officer
Learn more about the organization at https://jobs.iqvia.com.
Job Overview
Position: Regulatory Affairs Officer
Location: Bangalore, India
Job Requisition ID: R1500693
Employment Type: Full-Time
Application Deadline: November 1, 2025 (Apply Soon)
Work Schedule: Standard (Monday to Friday)
As a Regulatory Affairs Officer, you will work under general supervision to prepare and review regulatory submission documents, supporting both clinical trial and marketing authorization activities for internal and external clients. You will also assist in managing day-to-day regulatory operations, ensuring that projects are completed efficiently and in compliance with international regulatory standards. IQVIA Hiring for Regulatory Affairs Officer
Key Responsibilities
The Regulatory Affairs Officer will be responsible for a range of duties supporting regulatory submissions, compliance, and project coordination. Key functions include: IQVIA Hiring for Regulatory Affairs Officer
1. Regulatory Documentation and Support
- Prepare, review, and manage regulatory documentation for clinical trials and product registrations.
- Ensure that all regulatory submissions comply with applicable guidelines and client requirements.
- Support Chemistry, Manufacturing, and Controls (CMC), Lifecycle Maintenance, Marketing Authorization Transfers, and Labeling projects.
- Provide guidance to internal and external teams regarding regulatory expectations and documentation standards.
2. Project Management and Collaboration
- Act as a Regulatory Team Member on small to medium-scale regulatory projects.
- Collaborate with senior regulatory staff to manage project timelines, deliverables, and client communications.
- Identify project needs, implement client requests, and track milestones to ensure successful project completion.
- Participate in team meetings with internal and external clients and communicate confidently in straightforward regulatory matters.
- IQVIA Hiring for Regulatory Affairs Officer
3. Quality and Compliance
- Maintain a strong understanding of applicable laws, regulations, and global regulatory frameworks.
- Support the development and maintenance of Standard Operating Procedures (SOPs) to ensure compliance with regulatory standards.
- Identify areas for process improvement and contribute to the enhancement of systems and workflows.
- Ensure audit readiness and maintain accurate records of submissions and communications.
4. Training and Development
- Support internal training sessions and assist in preparing training materials related to regulatory procedures.
- Participate in knowledge-sharing initiatives to build regulatory expertise within the organization.
- Stay updated with the latest regulatory guidelines, including changes to international standards affecting clinical and marketing submissions.
5. Client Interaction and Communication
- Support business development efforts by preparing background materials and presentations for client meetings.
- Communicate effectively with clients to address queries, provide updates, and ensure alignment on project goals.
- Collaborate across departments, including clinical, quality, and project management teams, to achieve regulatory success.
Required Qualifications and Experience
To be considered for the Regulatory Affairs Officer position, candidates must meet the following educational and professional requirements: IQVIA Hiring for Regulatory Affairs Officer
Education
- Bachelor’s Degree in Life Sciences, Pharmacy, or a related discipline (Required)
- Master’s Degree in Life Sciences or related field (Preferred)
Experience
- At least 2 years of relevant experience in regulatory affairs, clinical research, or pharmaceutical development.
- Practical experience with CMC documentation, labeling, or marketing authorization submissions.
- Good understanding of the Research and Development (R&D) process, including preclinical, clinical, and manufacturing stages.
Technical Skills
- Proficient in Microsoft Office and relevant publishing tools used for regulatory documentation.
- Strong writing and editing skills for technical and scientific documents.
- Ability to manage multiple projects under supervision, ensuring accuracy and adherence to timelines.
- Knowledge of international regulatory frameworks, including ICH, EMA, and FDA requirements.
Soft Skills
- Excellent verbal and written communication abilities.
- Strong organizational and time management skills.
- Self-motivated with a strong desire to learn and grow in the regulatory domain.
- Demonstrated ability to work collaboratively within cross-functional teams.
Key Competencies
- Attention to detail: Accuracy in preparing and reviewing regulatory documents.
- Regulatory knowledge: Understanding of guidelines governing product development, clinical trials, and post-marketing activities.
- Collaboration: Ability to coordinate with teams across multiple departments and geographic locations.
- Adaptability: Capability to adjust quickly to changing project requirements and timelines.
- Problem-solving: Analytical mindset with the ability to identify solutions to regulatory challenges.
Why Join IQVIA?
Working at IQVIA means becoming part of a global community dedicated to driving innovation in healthcare and improving lives around the world. As a Regulatory Affairs Officer, you will have the opportunity to work on groundbreaking projects that shape the future of pharmaceuticals and clinical research. IQVIA Hiring for Regulatory Affairs Officer
Benefits of joining IQVIA include:
- Exposure to global regulatory operations and international markets.
- Opportunities to grow professionally in a dynamic, fast-paced environment.
- Collaborative and inclusive workplace culture.
- Access to advanced technology tools for regulatory and clinical operations.
- Career advancement through structured learning and mentorship programs.
At IQVIA, employees are encouraged to think creatively, contribute ideas, and drive positive change across the organization. IQVIA Hiring for Regulatory Affairs Officer
About the Work Environment
- Location: Bangalore, India
- Type: Full-Time (Onsite)
- Department: Regulatory Affairs
- Schedule: Standard working hours, Monday to Friday
The role is ideal for professionals who thrive in structured, team-based environments and who enjoy contributing to projects that have a global impact on healthcare and medicine. IQVIA Hiring for Regulatory Affairs Officer
Equal Employment Opportunity (EEO)
IQVIA is an Equal Employment Opportunity (EEO) employer committed to diversity and inclusion. The company does not discriminate based on race, religion, gender, sexual orientation, national origin, disability, or veteran status.
IQVIA also provides accessibility assistance to candidates with disabilities during the hiring process. Applicants requiring accommodations can contact the dedicated accessibility service via the phone number provided on the careers website. IQVIA Hiring for Regulatory Affairs Officer
How to Apply
If you are passionate about regulatory affairs and want to contribute to the global healthcare and life sciences industry, follow these steps to apply for the Regulatory Affairs Officer position at IQVIA:
- Visit the official IQVIA careers page: https://jobs.iqvia.com
- Search for the job title “Regulatory Affairs Officer” or use the Job Requisition ID: R1500693.
- Review the detailed job description and qualifications.
- Click “Apply Now” and sign in (or create an account) to start your application.
- Complete the application form, upload your updated resume, and submit before the deadline on November 1, 2025.
Start your journey with IQVIA today — where your expertise in regulatory affairs can help accelerate innovation and improve healthcare outcomes worldwide. IQVIA Hiring for Regulatory Affairs Officer
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