Regulatory/Sr Regulatory Associate Hiring at Syneos Health

Regulatory/Sr Regulatory Associate Jobs in Gurugram – Apply Now for Pharma Graduates Explore Regulatory/Sr Regulatory Associate vacancies at Syneos Health in Gurugram. Openings for BS/BA graduates with 2–4 years’ experience. Apply now for top pharma jobs!

Regulatory/Sr Regulatory Associate Careers at Syneos Health, Gurugram

If you are a pharma graduate seeking dynamic career growth in regulatory affairs, Syneos Health offers a compelling opportunity as a Regulatory/Sr Regulatory Associate (Module 1, Regulatory Submission) at its Gurugram, India location. Syneos Health is a global leader in biopharmaceutical solutions, renowned for accelerating the development and delivery of innovative therapies. With a presence in over 110 countries and a workforce of 29,000 professionals, Syneos Health is the ideal place to advance your regulatory career.

Why Choose Syneos Health?

• Work with a company that has contributed to 94% of all novel FDA-approved drugs in the past five years.

• Be part of a collaborative, product development-focused team that values innovation, diversity, and personal growth.

• Experience a supportive culture that prioritizes career development, training, and employee well-being.

Job Overview: Regulatory/Sr Regulatory Associate (Module 1, Regulatory Submission)

Location: Gurugram, India (Hybrid)

Syneos Health is hiring talented professionals for its Regulatory/Sr Regulatory Associate position, focusing on Module 1 regulatory submissions. This role is perfect for candidates with a BS/BA degree (or equivalent) and 2–4 years of regulatory experience, especially those familiar with Veeva Vault and Regulatory Information Management Systems (RIMS).

Key Responsibilities

• Interpret health authority approval letters and update registration data for both marketed and investigational products.

• Independently manage the intake, archival, and extraction of data from health authority correspondence.

• Ensure accurate data entry into RIM systems, supporting content plans and registration records.

• Coordinate data review with relevant stakeholders to meet reporting timelines.

• Identify and escalate non-compliance or quality issues to the Regulatory Information Management team.

• Deliver high-quality information processing within tight deadlines, adhering to standard operating procedures.

• Support project-specific activities with minimal supervision, managing multiple concurrent assignments.

• Build and maintain client relationships, attending meetings as required.

• Review and track the performance of regulatory associates, collaborating with project managers and directors.

• Mentor and train team members as needed.

• Maintain up-to-date training records and complete all mandatory training.

Required Qualifications

Candidates from the following educational backgrounds are encouraged to apply:

• B Pharm, M.Pharm, BSc. (Life Sciences), MSc. (Biotechnology, Microbiology, Biochemistry)

• Pharm.D, B.Tech/M.Tech (Biotechnology), BDS, MBBS (with regulatory experience)

• Postgraduate diplomas in Regulatory Affairs, Clinical Research, or related fields

• 2–4 years of relevant regulatory experience, with at least 2 years in Veeva Vault and RIMS.

• Strong analytical, interpersonal, and communication skills.

• Advanced proficiency in Microsoft Office applications.

• Ability to work independently, follow detailed instructions, and manage multiple projects.

• Fluent in English (spoken and written).

What Makes This Role Stand Out?

• Global Impact: Work on projects that contribute to the approval and delivery of life-changing therapies worldwide.

• Career Progression: Access to technical and therapeutic training, peer recognition, and advancement opportunities.

• Inclusive Culture: Thrive in a diverse, supportive environment that values your unique background and perspective.

• Hybrid Work Model: Enjoy flexibility with a hybrid work arrangement in Gurugram.

How to Apply

If you are a qualified professional passionate about regulatory affairs and ready to make a difference in the pharma industry, Syneos Health wants to hear from you. Click “Apply Now” to join a team where your expertise matters and your career can flourish.

Frequently Asked Questions

What educational qualifications are required?
A BS/BA degree in pharmacy, life sciences, or a related discipline, or equivalent practical experience.

Is experience mandatory?
Yes, 2–4 years of regulatory experience is required, with at least 2 years in Veeva Vault and RIMS.

Where is the job located?
Gurugram, India, with a hybrid work model.

What are the key skills needed?
Analytical skills, attention to detail, advanced Microsoft Office proficiency, and strong communication abilities.

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