Summary
Overview
Work History
Education
Skills
Certification
Key Oncology Trial Experience
Timeline
Generic
FAHEEMA PARVEEN

FAHEEMA PARVEEN

Senior Clinical Research Associate
New Delhi

Summary

Experienced clinical research professional with a proven track record of successfully managing and monitoring clinical trials for over 6 years. Specializes in site initiation, patient recruitment, data management, and ensuring regulatory compliance. Experienced in coordinating multi-site trials, maintaining quality standards, and facilitating effective communication with stakeholders. Dedicated to upholding ethical practices and ensuring efficient execution of clinical research projects.

Overview

6
6
years of professional experience
4
4
Certifications

Work History

Senior Executive-Clinical Research (Sr. CRA)

Meril Life Sciences
05.2024 - 05.2025
  • Lead and monitor multi-center oncology trials, including CAR-T therapy studies, ensuring protocol compliance, regulatory adherence, and effective cross-functional coordination across stakeholders.
  • Collaborate with investigators, ethics committees, and sponsors, managing essential documentation and regulatory requirements while proactively resolving site-level challenges.
  • Experienced in all phases of oncology trials, including global studies, with a strong interest in transitioning to a centralized role to leverage coordination and monitoring expertise.

Assistant Manager/CRA- Oncology Clinical Research

Max Super Specialty Hospital
06.2023 - 05.2024
  • Conducted routine monitoring visits to ensure protocol adherence, GCP compliance, and proper documentation of informed consent across study sites.
  • Collaborated with site staff to address patient recruitment challenges, while overseeing timely and accurate reporting of AEs and SAEs.
  • Reviewed and maintained essential regulatory documents, including IRB/IEC approvals, ICFs, and delegation logs, ensuring compliance throughout the study lifecycle.

Clinical Research Coordinator

All India Institute of Medical Sciences (AIIMS)
11.2020 - 06.2023
  • Conducted study visits in compliance with ICH/GCP and FDA regulations, assessed patient eligibility per protocol, completed CRFs, and accurately extracted source data to support study integrity.
  • Collaborated with principal investigators, sponsors, and site staff to facilitate daily trial activities, coordinated subject appointments, and served as a liaison to ensure smooth patient and physician engagement.
  • Participated in pre-study, initiation, monitoring, and closeout visits; monitored patient safety and reported AEs/SAEs; assisted with regulatory submissions, including IRB approvals, ensuring ongoing compliance.

Clinical Research Coordinator

Max Super Specialty Hospital
05.2019 - 11.2020
  • Created and maintained clinical trial databases and study documentation.
  • Coordinated trial closures, final data analysis, and study reporting.

Education

MBA - Pharmaceutical Management

Jamia Hamdard University
New Delhi, DL

Bachelor in Pharmacy - undefined

Jamia Hamdard University
New Delhi, DL

Diploma in Pharmacy - undefined

Jamia Hamdard University
New Delhi, DL

Skills

  • Knowledge of clinical trial regulations
  • Protocol adherence expertise
  • Informed consent management
  • Experience with AE/SAE tracking
  • Readiness assessment for audits
  • Management of clinical trial processes
  • Regulatory document management

Certification

Advanced P.G. Diploma in Clinical Research & Clinical Data Management (CDM), Clinosoft Research

Key Oncology Trial Experience

  • Navigate Study, Phase II, Breast & Lung
  • Aranote Study, Phase III, Prostate
  • Darolutamide, Phase IV, Prostate
  • Veritac Study, Phase III, Breast
  • CART-NAL, Phase 1 & 2, NHL & ALL
  • Apollo PMS, Phase IV, Brain, Lung, Ovarian
  • Trumab, Phase III, Breast
  • MyeloCART, Phase 1, Multiple Myeloma

Timeline

Senior Executive-Clinical Research (Sr. CRA)

Meril Life Sciences
05.2024 - 05.2025

Assistant Manager/CRA- Oncology Clinical Research

Max Super Specialty Hospital
06.2023 - 05.2024
Advanced P.G. Diploma in Clinical Research & Clinical Data Management (CDM), Clinosoft Research
04-2023

Clinical Research Coordinator

All India Institute of Medical Sciences (AIIMS)
11.2020 - 06.2023

Clinical Research Coordinator

Max Super Specialty Hospital
05.2019 - 11.2020

Bachelor in Pharmacy - undefined

Jamia Hamdard University

Diploma in Pharmacy - undefined

Jamia Hamdard University

MBA - Pharmaceutical Management

Jamia Hamdard University
FAHEEMA PARVEENSenior Clinical Research Associate