Minakshi Chauhan profile photo 1 on Tal

Minakshi Chauhan

Clinical Research Associate @ Patanjali Research Foundation

Dehradun

2+ years of work experience

Patanjali Research Foundation
Jan 20266 mosPresent

Haridwar

• Managed end-to-end monitoring activities for Ayurveda and integrative medicine clinical studies. • Ensured regulatory and protocol compliance under AYUSH-GCP standards through meticulous oversight. • Conducted Source Data Verification (SDV) to maintain data accuracy and integrity across CRFs and source documents. • Collaborated with investigators and quality assurance teams to uphold ICH-GCP and AYUSH regulatory adherence.
Auriga Research Private Limited
Jan 20251 yr 1 moJan 2026

Conducted 30+ monitoring visits including SIV, IMV, and Close-Out Visits for clinical studies. Performed SDV to ensure protocol compliance, subject safety, and accurate clinical data collection. Maintained TMF/eTMF documentation and ensured inspection readiness. Collaborated with investigators and site coordinators for query resolution and study progress tracking. Assisted during audits and inspections while ensuring compliance with ICH-GCP standards.
Auriga Research Private Limited
Aug 20246 mosJan 2025

Supported Phase II nutraceutical clinical trials from study start-up to close-out. Assisted in preparation and version control of Protocols, CRFs, and ICFs. Managed investigational product tracking and essential document collection. Coordinated communication between CRAs, investigators, and study teams.
Auriga Research Private Limited
Feb 20247 mosAug 2024

• Assisted in the organization of the Trial Master File (TMF) and regulatory file management in compliance with SOPs and ICH-GCP. • Supported data entry, Case Report Form (CRF) tracking, and query follow-up under the supervision of Clinical Research Associates (CRAs). • Gained hands-on experience in site management, data quality control, and regulatory operations at Auriga Research Private Ltd.

Education

Swami Rama Himalayan University

Masters degree, Clinical Research

Swami Rama Himalayan University

20222 yrs2024
Hemvati Nandan Bahuguna Garhwal University ( A Central University )

Bechlors, Microbiology, Botany, Zoology

Hemvati Nandan Bahuguna Garhwal University ( A Central University )

20193 yrs2022

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Headline

Clinical Research Associate @ Patanjali Research Foundation

About

Clinical Research professional with 2.5+ years of cumulative experience across clinical trial operations, site monitoring, regulatory documentation, and clinical data review in BA/BE studies, oncology, endocrinology, nutraceutical, and Ayurveda-integrative medicine trials. Currently working as a Clinical Research Associate at Patanjali Research Foundation, managing monitoring activities and ensuring protocol compliance under AYUSH-GCP and ICH-GCP standards. Previously associated with Auriga Research Pvt. Ltd., where I conducted 30+ on-site and remote monitoring visits including Site Initiation Visits (SIV), Interim Monitoring Visits (IMV), and Close-Out Visits (COV). Experienced in Source Data Verification (SDV), TMF/eTMF maintenance, regulatory documentation, audit readiness, and investigator coordination.

Location

Dehradun

Work experience

Clinical Research Associate at Patanjali Research Foundation, Jan 2026 - Present · 6 mos, Haridwar, • Managed end-to-end monitoring activities for Ayurveda and integrative medicine clinical studies. • Ensured regulatory and protocol compliance under AYUSH-GCP standards through meticulous oversight. • Conducted Source Data Verification (SDV) to maintain data accuracy and integrity across CRFs and source documents. • Collaborated with investigators and quality assurance teams to uphold ICH-GCP and AYUSH regulatory adherence.

Clinical Research Associate at Auriga Research Private Limited, Jan 2025 - Jan 2026 · 1 yr 1 mo, Conducted 30+ monitoring visits including SIV, IMV, and Close-Out Visits for clinical studies. Performed SDV to ensure protocol compliance, subject safety, and accurate clinical data collection. Maintained TMF/eTMF documentation and ensured inspection readiness. Collaborated with investigators and site coordinators for query resolution and study progress tracking. Assisted during audits and inspections while ensuring compliance with ICH-GCP standards.

Clinical Trial Assistant at Auriga Research Private Limited, Aug 2024 - Jan 2025 · 6 mos, Supported Phase II nutraceutical clinical trials from study start-up to close-out. Assisted in preparation and version control of Protocols, CRFs, and ICFs. Managed investigational product tracking and essential document collection. Coordinated communication between CRAs, investigators, and study teams.

Clinical Research Intern at Auriga Research Private Limited, Feb 2024 - Aug 2024 · 7 mos, • Assisted in the organization of the Trial Master File (TMF) and regulatory file management in compliance with SOPs and ICH-GCP. • Supported data entry, Case Report Form (CRF) tracking, and query follow-up under the supervision of Clinical Research Associates (CRAs). • Gained hands-on experience in site management, data quality control, and regulatory operations at Auriga Research Private Ltd.

Education

Masters degree, Clinical Research, Swami Rama Himalayan University

Bechlors, Microbiology, Botany, Zoology, Hemvati Nandan Bahuguna Garhwal University ( A Central University )