Regulatory Technology Analyst CLIN BIOSCIENCES
CLIN BIOSCIENCES
Office Location
Full Time
Experience: 1 - 1 years required
Pay: INR 2200000 - INR 3400000 /year
Type: Full Time
Location: Hyderabad
Skills: HealthTech, pharmacompliance, regulatoryaffairs, drugsubmissions, lifesciencesit, regulatoryit, regulatorytech
About CLIN BIOSCIENCES
Job Description
Roles and Responsibilities
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Implement and manage Regulatory Information Management Systems and eCTD platforms
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Automate regulatory submission workflows, ensuring compliance.
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Work with regulatory affairs teams to manage submission timelines and document lifecycle
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Configure and support Veeva Vault RIM, Liquent Insight, EXTEDO, or other regulatory platforms
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Extract, validate, and analyze structured data from submissions and global regulatory databases
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Assist in audit readiness, quality assurance, and compliance tracking
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Coordinate with IT and compliance teams for system upgrades, validations, and user training
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Monitor global regulatory changes and ensure systems are aligned to evolving requirements
Qualifications
- Bachelor's or Masters in Life Sciences, Pharmacy, Biotechnology, Computer Science, or related discipline
- Experience with regulatory affairs workflows and technology tools.
- Certifications in regulatory affairs (RAC), Veeva Vault, or similar are a plus.
- Excellent communication and interpersonal skills.
- Ability to work independently and as part of a team.
Interested to apply can share CV or call/WhatsApp to 9384592766