AHMEDABAD · FULLTIME
Regulatory Analyst

cliantha research ltd
Ahmedabad · onsite · Posted 4d ago
Sourced from
Undisclosed4–7 yrsfulltimeAhmedabad
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Section · 01
About this role
Key Responsibilities
- Prepare responses to regulatory inspections and client audit observations and submit it within a defined timeline.
- Collaborate with QA and Bioanalytical teams to collect, review, and compile data required for regulatory and audit responses.
- Track compliance commitments and ensure their effective implementation.
- Support in-process and retrospective bioanalytical monitoring activities.
Host client site qualification visits and confidently present laboratory capabilities and compliance systems
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Section · 02
Skills
Regulatory Auditsclinical researchregulatoryRegulatory Affairsregulatory submissionsregulatory requirementsMethod DevelopmentMethod ValidationRegulatory Guidelinesregulatory operationsbioanalyticalRegulatory ReportingRegulatory Compliance
Section · Company
About Cliantha Research

cliantha research ltd
Clinical Research
894
employees
2004
22 years old
Ahmedabad, Gujrat
India
₹4.8L PA avg
Avg at Cliantha Research
About
Cliantha Research is a Clinical Research Organization offering comprehensive services aimed at ensuring regulatory compliance in clinical trials across various therapeutic areas.
Industries
Clinical ResearchBiotech & Life sciencesAnalytics & KPO
Employee ratings
10 reviews
4.1/ 5
Culture
3.6
Career growth
3.2
Work-life
3.9
Employees rate it well for
Job Security44Overall Company41
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