Dr.ABUZEAR IMAM FARUQUI
CLINICAL RESEARCH QC COORDINATOR (Lead)
BANGALORE
Summary
Certified Clinical Research Coordinator with a solid background in clinical trials and data management. Seeking to transition into a Clinical Research Associate role to utilize clinical expertise in ensuring protocol compliance and data integrity. Proactive and detail-oriented professional, highly supportive and enthusiastic, always striving for excellence in clinical research. Committed to expanding knowledge in clinical monitoring and site management, dedicated to contributing to the success of clinical trials and advancing patient care through meticulous oversight and continuous learning.
Overview
3
3
years of professional experience
6
6
years of post-secondary education
5
5
Certifications
Work History
Clinical Research QC Coordinator
Kalkon Clinical Pvt. Ltd
11.2021 - Current
- Utilized Clinical Trial Management System (CTMS) software to retrieve patient data, review reports, and manage patient data. .
- Administered screening process for subject enrollment, ensuring compliance with protocol requirements and regulatory standards.
- Conducted Source Document Review (SDR) and manual data review, verifying accuracy and completeness of clinical data in CRFs.
- Managed and resolved data queries, driving query resolution to closure within agreed timelines to maintain data integrity.
- Maintained eDiary responses and tracked adverse events using eDiary portal, ensuring adherence to study protocols.
- Collaborated with Key Opinion Leaders (KOLs) and site staff to foster strong professional relationships and ensure alignment with clinical objectives.
- Conducted vendor reconciliations to ensure accuracy and consistency in data management, supporting audit readiness and regulatory compliance.
- Delivered frequent and detailed updates to management, providing transparency on project progress and ensuring adherence to timelines and budgets.
- Identified and mitigated potential risks related to site performance and data integrity through proactive monitoring and regular communication with site staff.
- Provided training and mentorship to junior clinical research staff, enhancing their understanding of clinical trial processes and data entry.
Education
Doctor of Pharmacy - Pharmacy
RAMAIAH UNIVERSITY OF APPLIED SCIENCE, Represented University
Bangalore 08.2014 - 07.2020
Skills
CTMS data review
GCP
Quality Assurance
MS Office
Resource optimization
Documentation Review
Quality control techniques
Problem-Solving
Teamwork and Collaboration
Strong Work Ethic
Decision-Making
Languages
English
Upper intermediate (B2)
Hindi
Excellent
Urdu
Excellent
Kannada
Average
Software
IMedidata EDC
Inform EDC
Veeva Vault
Imednet
Advanced MD(EHR)
Athenanet(EHR)
Kareo(EHR)
CRIO(CTMS)
IQVIA(e-Consent)
Zelta EDC
Labcorp Lab portal
Clario Ecg portal
PPD Lab portal
Autocruitment Referal portal
Subject well Referal porta
Clinical conductor CTMS
ECW EMR
Walgreens Referal portal
Onco EMR
Accomplishments
- Ensured Study Maintenance: Provided comprehensive training to over 5 Clinical Research Coordinators (CRCs), ensuring they were well-equipped to execute their roles effectively, which contributed to the successful management of more than 50 studies across various major therapeutic areas.
- Effective Discrepancy Monitoring: Vigilantly monitored discrepancies and promptly resolved over 800 data queries, ensuring the accuracy and reliability of study data and maintaining compliance with regulatory standards.
- Timely Issue Resolution: Proactively addressed and resolved study-related issues within 24 hours on average, preventing disruptions and ensuring smooth project progression across multiple clinical trials.
- Project Management in Orthopaedics and Physiotherapy: Led a 7-month project in the Department of Orthopaedics and Physiotherapy, focusing on the critical evaluation of prescribing patterns, which improved medication management practices.
- Clinical Pharmacology Experience: Worked as a Clinical Pharmacologist across multiple departments, including General Medicine (4 months), Respiratory Medicine (2 months), Orthopedics (2 months), Surgery (2 months), Oncology (1 month), and Pediatrics (1 month). Conducted over 150 critical evaluations of prescribing patterns, Medication History Interviews (MHI), Pharmacoeconomics assessments, and patient counseling sessions.
- Protocol and ICF Development: Developed protocols and Informed Consent Forms (ICF) for multiple projects, ensuring adherence to regulatory requirements and ethical standards.
- Chief Investigator Role: Served as the Chief Investigator for a study on deprescribing analgesics in patients with knee osteoarthritis, leading to the successful implementation of a physiotherapy-based treatment plan that improved patient Quality of Life (QoL) by 20% within one month.
- Literature Review: Conducted comprehensive literature reviews for project development, contributing to evidence-based decision-making and study design.
Certification
Medidata Classic Rave Certified Clinical Research Coordinator
Publications
Deprescribing of analgesics and replacement with physiotherapy in the department of orthopedics for knee osteoarthritis patients deprescribing of analgesics and replacement with physiotherapy in the department of orthopedics for knee osteoarthritis patients.
Value in health-elisever publication · Nov 9, 2019
Timeline
Good Clinical Practice(GCP)
11-2024
Medidata Classic Rave Certified Clinical Research Coordinator
07-2024
Crash course in Clinical Research and Pharmacovigilancesite training Certificate.
03-2022
Clinical Research QC Coordinator
Kalkon Clinical Pvt. Ltd
11.2021 - Current
CRIO CTMS Training certification
11-2021
Good Clinical Practice(GCP)
11-2021
Doctor of Pharmacy - Pharmacy
RAMAIAH UNIVERSITY OF APPLIED SCIENCE, Represented University
08.2014 - 07.2020
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