Open to opportunities

madhuri vaishnava

@madhurivaishnava

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Clinical research scientist specializing in drug safety, pharmacovigilance, and trial coordination.

India

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What I'm looking for

I am seeking clinical research or pharmacovigilance roles where I can lead trial coordination, ensure regulatory compliance, and contribute to impactful, patient-focused studies with collaborative teams and clear opportunities for scientific growth.

I am a dedicated healthcare professional with a Master’s in Drug Design and Discovery and a Doctor of Pharmacy, bringing hands-on experience across clinical research, pharmacovigilance, nanomedicine, and pharmaceutical sciences.

I have supported clinical trial protocol implementation, managed CRFs and source documentation per ICH-GCP, coordinated ethics submissions, and worked with CROs and multi-site teams to ensure timely study enrolment and data integrity.

My technical strengths include analytical laboratory techniques (HPLC, UV, TLC, SDS-PAGE), cell culture and cytotoxicity assays, MedDRA/WHO coding, Argus Safety, and EDC tools; I am also a Registered Pharmacist with strong documentation and time-management skills.

I have contributed to clinical trials and research projects including Phase III and IV studies, nanoparticle interaction research, and prospective registries, and I aim to apply my scientific rigor and coordination skills to advance patient-centered clinical research.

Experience

Work history, roles, and key accomplishments

Current

Project Research Scientist

Current

Nizam's Institute of Medical Sciences

Nov 2024 - Present (1 year 2 months)

Supported clinical trial protocol implementation and regulatory compliance, managed CRFs and source documents per ICH-GCP, and contributed to literature reviews and ICMR progress reports.

Clinical Trial Management ICH GCP CRF Regulatory Ethics Submissions Data Management

Clinical Research Coordinator

Nizam's Institute of Medical Sciences

Jul 2024 - Sep 2024 (2 months)

Coordinated site activities with CROs and hospital staff, pre-screened subjects to support study enrolment, and maintained Site Master File and essential study documents.

Research Assistant

All India Institute of Medical Sciences

May 2023 - Dec 2023 (7 months)

Recruited participants, collected and managed study data, coordinated multi-site teams to monitor progress, and assisted in reporting and literature reviews.

Data Collection literature review

Pharmacy Advisor

Walgreens Boots Alliance

Oct 2022 - Dec 2022 (2 months)

Dispensed medications, provided pharmaceutical guidance and medication therapy management, and counselled patients on safe medicine use.

Patient Counselling Medication Management

Drug Safety Associate

Vigilare Biopharma

Mar 2019 - Feb 2020 (11 months)

Maintained EDC and clinical databases, supported case processing in Argus Safety, and assisted in signal detection, MedDRA coding, and adverse event reporting.

Pharmacovigilance MedDRA Signal Detection Adverse Events

Clinical Research Intern

Sunshine Hospitals

Jul 2018 - Jul 2019 (1 year)

Validated clinical data, managed queries and TMF documents, participated in ward rounds and ADR reporting, and supported patient counselling for rational medication use.

TMF Patient Counselling Query Management