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Nidanaaz Momin

@nidanaazmomin

Clinical Trial Operations professional transitioning to sponsor-side roles, coordinating trial documentation and inspection readiness.

India

Message

What I'm looking for

I’m transitioning toward sponsor-side Clinical Trial Operations and Drug Regulatory Affairs roles, where I can support protocol-compliant study delivery, regulatory documentation, audit readiness, and collaboration with investigators, CROs, and sponsors.

At Cytespace Research Pvt Ltd, I coordinated site initiation, monitoring readiness, sponsor visits, and close-out processes. I managed Trial Master File and regulatory documentation, coordinated ethics committee submissions, and supported CRF/eCRF data workflows and query resolution.

At Dr. Neeta Mehta’s Clinic, I coordinated neurology and gastrointestinal clinical trials, from participant screening and consent documentation through monitoring visits and close-out. I’m now pursuing a Ph.D. in Public Health at Datta Meghe Institute of Health Sciences, with ongoing research focused on breast cancer epidemiology.

Experience

Work history, roles, and key accomplishments

Current

Ph.D. Student – Public Health Research

Current

Datta Meghe Institute of Health Sciences

Jan 2024 - Present (2 years 10 months)

Leading ongoing research focused on breast cancer epidemiology, including study design planning, literature review, and analytical evaluation.

Epidemiology Public Health Research Study Design literature review Data Analysis

Master of Public Health Student – School of Epidemiology

Datta Meghe Institute of Health Sciences

Jan 2021 - Dec 2023 (2 years 11 months)

Executed research projects including Cancer Epidemiology in India, conducted field practicum on breast cancer public health assessment, and performed secondary epidemiological studies.

Epidemiology Public Health Research Data Analysis Field Research

Consultant Research Analyst

IMRB International (Kantar Health)

Jan 2015 - Jul 2016 (1 year 6 months)

Conducted epidemiological research and healthcare data analysis, produced analytical summaries and project reports, and coordinated project timelines and quality checks.

Epidemiology Healthcare Data Analysis Research Project Coordination Reporting

Site Solutions Executive – Clinical Research Operations

Cytespace Research Pvt Ltd

Sep 2014 - Dec 2014 (3 months)

Coordinated site initiation, monitoring readiness, QA activities, sponsor visits, and close-out processes. Managed Trial Master File and regulatory documentation, ethics committee submissions, and CRF/eCRF data workflows.

Clinical Research Trial Master File Regulatory Documentation Ethics Submissions CRF Data Query Resolution ICH GCP

Clinical Research Coordinator

Dr. Neeta Mehta’s Clinic

May 2012 - Sep 2014 (2 years 4 months)

Coordinated operational execution of neurology and gastrointestinal clinical trials, managed participant screening, enrollment, and follow-up, and ensured regulatory compliance and audit readiness.

Clinical Trials Neurology Gastroenterology Participant Screening Informed Consent Forms Regulatory Compliance Adverse Event Reporting ICH GCP

Assistant Doctor

Dr. Aparna’s Clinic

Nov 2011 - Jun 2013 (1 year 7 months)

Conducted patient case evaluations and follow-up management, and maintained clinical documentation and treatment records.

Patient Care Clinical Documentation Case Evaluations

Education

Degrees, certifications, and relevant coursework

Datta Meghe Institute of Health Sciences

Ph.D., Public Health

2024 -

Ongoing Ph.D. in Public Health focusing on breast cancer epidemiology, including study design, literature review, and analytical evaluation.

Datta Meghe Institute of Health Sciences

Master of Public Health, Public Health

2021 - 2023

Master of Public Health from the School of Epidemiology, with research projects including cancer epidemiology in India and a field practicum on breast cancer public health assessment.