Summary
Overview
Work History
Education
Skills
Websites
Skills And Certifications
Certification
Timeline
Generic

Samin Chopra

Queens

Summary

Results-oriented Oncology Clinical Research Supervisor with expertise in protocol implementation and clinical trial management. Enhances study execution and compliance through cross-functional collaboration and mentorship. Utilizes Medidata Rave to maintain data integrity and promote accountability within research teams.

Overview

7
7
years of professional experience
1
1
Certification

Work History

Oncology Clinical Research Supervisor

Northwell Cancer Institute
New York
12.2025 - Current
  • Led planning, implementation, and execution of clinical trial activities across oncology and Phase I portfolios.
  • Oversaw study start-up, conduct, and close-out activities, ensuring adherence to timelines, enrollment targets, and data quality expectations.
  • Co-led study team discussions with investigators and operational partners to align study objectives; collaborated cross-functionally with safety data, regulatory, and sponsor teams to enhance study execution.
  • Provided matrix leadership to clinical research coordinators and support staff; educated team members on protocol requirements, study conduct, and GCP/ICH compliance.
  • Acted as the primary site-facing contact for clinical and protocol-related inquiries, escalating scientific or safety concerns to investigators and sponsors.
  • Reviewed clinical narratives and safety documentation to uphold high standards for AE/SAE reporting and ensure data consistency.
  • Supervised research teams to maintain compliance with protocols and regulations while coordinating timelines across multiple studies.
  • Supported sponsor budget planning and CRO coordination by providing protocol-specific operational input.

Oncology Senior Clinical Research Coordinator

Northwell Cancer Institute
New York
06.2025 - 12.2025
  • Led execution of multiple oncology and Phase I basket trials with minimal supervision, ensuring protocol adherence and data integrity.
  • Managed clinical data review, discrepancy identification, and query resolution within EDC systems, ensuring data accuracy and integrity.
  • Mentored coordinators on protocol requirements, CRF completion, safety reporting, and monitoring readiness, enhancing team compliance and knowledge.
  • Supported protocol amendments, ICF updates, and cross-functional comment resolution in collaboration with regulatory and sponsor teams.
  • Facilitated sponsor-led study meetings, monitoring visits, and audit responses, contributing to effective communication and compliance.

Oncology Clinical Research Coordinator

Northwell Cancer Institute
New York
02.2023 - 05.2025
  • Managed day-to-day conduct of Phase I-III oncology clinical trials across Phase I basket and genitourinary disease teams.
  • Ensured accurate execution, data capture, and patient safety oversight for assigned protocols.
  • Coordinated study start-up, site initiation visits (SIVs), interim monitoring visits (IMVs), and close-out visits (COVs) to ensure compliance with regulatory standards.
  • Analyzed clinical data trends and safety signals; escalated critical findings to investigators, sponsors, and medical monitors to enhance patient safety.
  • Entered, reviewed, and validated clinical data in Medidata RAVE, InForm, REDCap, and ancillary systems; resolved queries and ensured data quality.
  • Contributed to protocol and ICF review processes, identifying operational and clinical considerations for sponsors and investigators.
  • Collaborated with pharmaceutical sponsors, CROs, investigators, project managers, and external vendors to streamline communication and project execution.
  • Supported development of site training materials and investigator meeting preparation.

Oncology Clinical Research Assistant

Northwell Cancer Institute
New York
12.2021 - 01.2023
  • Facilitated clinical data generation and validation for oncology trials to ensure accuracy and compliance.
  • Coordinated with cross-functional teams to meet protocol timelines and uphold study quality objectives.
  • Conducted monitoring visits and prepared for audits while maintaining comprehensive source documentation.

Research Technician

Feinstein Institute
New York
07.2019 - 10.2020
  • Executed DNA extraction and quantification via spectrophotometry to ensure sample integrity for downstream applications.
  • Contributed to preclinical therapeutic research through data collection, analysis, and documentation to support study objectives.
  • Conducted experiments to support biomedical research initiatives at the Feinstein Institute.
  • Collected and analyzed data for ongoing clinical studies and trials.
  • Maintained and calibrated laboratory equipment for optimal performance and accuracy.

Education

Bachelor of Arts - Biology

Barnard College of Columbia University
New York
05.2019

Skills

  • Protocol implementation
  • Clinical trial leadership
  • Phase I oncology
  • Study start-up and close-out
  • Clinical data review
  • Adverse event management
  • Medical terminology expertise
  • GCP and ICH compliance
  • audit and inspection readiness
  • Medidata Rave proficiency
  • REDCap experience
  • Data review tools expertise
  • Oracle database management
  • ClinPhone usage
  • Parexel imaging knowledge
  • Triad collaboration
  • Electronic medical records management
  • Matrix team leadership
  • Cross-functional collaboration skills
  • Sponsor and CRO liaison
  • effective scientific communication
  • Training and mentorship programs
  • Project planning and execution

Skills And Certifications

Protocol Implementation, Clinical Trial Leadership, Phase I Oncology, Study Start-Up, Conduct & Close-Out, Clinical Data Review & Trend Identification, AE/SAE Management (CTCAE), RECIST, Medical Terminology, GCP/ICH, Audit & Inspection Readiness, Medidata RAVE, InForm, REDCap, J-Review-like data review tools, Oracle, ClinPhone, Parexel Imaging, Triad, EMR, Matrix Team Leadership, Cross-Functional Collaboration, Sponsor & CRO Liaison, Scientific Communication, Training & Mentorship, Project Planning, Certified Clinical Research Coordinator (CCRC), ACRP, 10/01/24, 11/01/26

Certification

Certified Clinical Research Coordinator CCRC ACRP

Timeline

Oncology Clinical Research Supervisor

Northwell Cancer Institute
12.2025 - Current

Oncology Senior Clinical Research Coordinator

Northwell Cancer Institute
06.2025 - 12.2025

Oncology Clinical Research Coordinator

Northwell Cancer Institute
02.2023 - 05.2025

Oncology Clinical Research Assistant

Northwell Cancer Institute
12.2021 - 01.2023

Research Technician

Feinstein Institute
07.2019 - 10.2020

Bachelor of Arts - Biology

Barnard College of Columbia University
Samin Chopra