Sankskrithi Murugan
Clinical & Safety Publishing | eCTD & Regulatory Documentation | GCP Certified | Experience with Veeva Vault (EDMS) | Advancing Expertise in Regulatory & Clinical Operations
- Role
- Associate Clinical and Safety Publisher at Novo Nordisk
- Location
- Bengaluru, KA, IN
- LinkedIn followers
- 500 followers
About Sankskrithi Murugan
Clinical research professional with experience in clinical and safety document publishing, regulatory submissions support, and end-to-end documentation management for global regulatory deliverables at Novo Nordisk. Skilled in eCTD-compliant document handling, electronic QC, EDMS (Veeva Vault), and coordination with cross-functional teams including Regulatory Affairs, Medical Writing, Biostatistics, and Clinical Operations.Previously trained in site-level clinical coordination (CRC), giving me a strong understanding of clinical trial execution, source documentation, ethics submissions, and GCP compliance from the ground level.I bring a blended background in Regulatory Documentation + Clinical Operations, making me well-suited for Regulatory Operations, Submission Publishing, CTA, In-House CRA, Clinical Documentation Specialist, or TMF roles in CROs.Core Skills:eCTD publishing · DSUR · PSUR · CTR · RMP · TMF docs · GCP documentation · Veeva Vault · eQC · Argus Safety · Regulatory compliance · Clinical trial workflow · Stakeholder coordination · SOP adherenceCertifications:ICH-GCP (Global Health Network) · PG Diploma in Clinical Research · Medical Terminology (Ongoing)Currently exploring CRO-based roles where I can expand my regulatory and clinical operations expertise while contributing to high-quality, compliant clinical submissions.
Experience
Associate Clinical and Safety Publisher
Jul 2025 — Present · Bangalore Urban, IN
Education
BSA Crescent Institute of Science and Technology
Bachelor of Science - BS, Biotechnology
REVA University
Master of Science - MS, Microbial Technology
Banglore Clinical Research Institute
PG Diploma , Clinical Research
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