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Murari Yatish

Centralize Monitoring | Risk-Based Monitoring (RBM) | Clinical Operations | CTMS | eTMF | Veeva Vault | Study Startup | Clinical Trial Management | R | SQL

New Delhi

3+ years of work experience

IQVIA
May 20242 yrs 3 mosPresent

• Collaborated as functional central monitor, resolve data issues and improve study performance. • Increased work efficiency by creating workflow for site follow up and IP reconciliation by using R. • iSP creation and site follow up. • Prepare documents for SIV and SSV. • Managed action items and protocol deviations in CTMS ensuring timely closure and compliance. • Supported 7+ clinical studies across startup, conduct, and closeout phases. • Generated iSP reports, prepared iSite packs, and maintained centralized monitoring documentation. • Conducted trend analysis on aging queries, KRIs, SDV backlog, and missing pages. • Performed Risk-Based Monitoring reviews using Clinical Analytics and CM platforms. • Managed eTMF systems migration and follow up on missing documents (Veeva Vault, Wingspan, sponsor specific). • Conducted subject-level data review and investigational product reconciliation. • Maintained site readiness, training compliance, and monitoring trackers. • Extracted SUSARs, investigator alerts, and regulatory reports from CTMS and DrugDev. • Supported financial operations including investigator payments, purchase orders, and invoice reconciliation.
Mar 20239 mosNov 2023

• Patient IP audit, IP indent and document reconciliation.

Education

Master's degree, Pharmacy

Kumaun University, Nainital

20212 yrs2023

Bachelor of Pharmacy, Pharmacology

Kumaon University Nainital, Uttarakhand

20183 yrs2021

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Headline

Centralize Monitoring | Risk-Based Monitoring (RBM) | Clinical Operations | CTMS | eTMF | Veeva Vault | Study Startup | Clinical Trial Management | R | SQL

About

Acquired skill and knowledge for positive growth.

Location

New Delhi

Work experience

clinical oprations at IQVIA, May 2024 - Present · 2 yrs 3 mos, • Collaborated as functional central monitor, resolve data issues and improve study performance. • Increased work efficiency by creating workflow for site follow up and IP reconciliation by using R. • iSP creation and site follow up. • Prepare documents for SIV and SSV. • Managed action items and protocol deviations in CTMS ensuring timely closure and compliance. • Supported 7+ clinical studies across startup, conduct, and closeout phases. • Generated iSP reports, prepared iSite packs, and maintained centralized monitoring documentation. • Conducted trend analysis on aging queries, KRIs, SDV backlog, and missing pages. • Performed Risk-Based Monitoring reviews using Clinical Analytics and CM platforms. • Managed eTMF systems migration and follow up on missing documents (Veeva Vault, Wingspan, sponsor specific). • Conducted subject-level data review and investigational product reconciliation. • Maintained site readiness, training compliance, and monitoring trackers. • Extracted SUSARs, investigator alerts, and regulatory reports from CTMS and DrugDev. • Supported financial operations including investigator payments, purchase orders, and invoice reconciliation.

Clinical Pharmacist at Mendanta Hospital, Mar 2023 - Nov 2023 · 9 mos, • Patient IP audit, IP indent and document reconciliation.

Education

Master's degree, Pharmacy, Kumaun University, Nainital

Bachelor of Pharmacy, Pharmacology, Kumaon University Nainital, Uttarakhand

Murari Yatish - clinical oprations in New Delhi | Tal