Experience

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  Modern healthcare hospital

  Jun 2014 - Jan 2015

  Clinical pharmacist

  Job Duties Includes:Prescription Review Drugs dispensingInventory ControlMedical Camp Organizer

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  Pakistan national joint registry (pnjr)

  Jan 2015 - Dec 2016

  Regional research coordinator (north)

  My responsibilites includes;1. Help the PI's to maintain their Registry account. 2. Monitor the Sites involved in the Registry3. Provide technical help in PNJR form filling.

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  Metrics research (pvt) ltd

  Jan 2015 - Dec 2016

  My responsibilities includes* Manage Global Multi-center Phase III Oncology Trials in Pakistan for Roche Pakistan* Monitor the Global Multicenter Phase III Oncology Trials in Pakistan for Roche Pakistan* Prepare Regulatory Documents for the Trials* Train the Trial Site Staff to conduct the trials according to the ICH-GCP Regulations* Provides Protocol, eCRF and other mandatory trainings to the Trial Site Staff. My responsibilities include1. Manage Global Multi-center Phase III and IV Trials: PHASE III Early Breast Cancer PHASE III Metastatic Breast Cancer 2. Monitor Observational study: Prevalence of Osteoporosis in Pakistan3. Involve in site management, monitoring, training of the site staff.

  • Lead /Sr. Clinical Research Associate (Roche Oncology Division)

    Jul 2016 - Dec 2016

  • Clinical Research Associate

    Jul 2015 - Jun 2016

  • Clinical Research Coordinator

    Jan 2015 - Jun 2015
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  Ferozsons laboratories limited

  Dec 2016 - Jan 2021

  Product Manager Cardio Metabolic - Diabetes Assistant Product Manager Hepatology

  • Product Manager

    Jul 2019 - Jan 2021

  • Assistant Product Manager

    Mar 2018 - Jun 2019

  • Clinical Research Associate

    Dec 2016 - Feb 2018
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  Drk pharma solutions gmbh

  Feb 2021 - Apr 2021

  Sr. clinical research associate/lead

  • Supervision of ongoing clinical research projects • eTMF preparation of Safeher and Peruse Trials (Roche Pakistan)• Monitoring of different ongoing Clinical Trials as a Compliance Officer• Development and writeup of study documents e.g., Clinical Trial Protocols, Case Report Form (CRF)• Locate and Assess the Feasibility of Sites• Liaise with Doctors, Consultants and Investigators conducting Trials.• Manage Regulatory Authority Applications and Approvals• Verify data on CRFs, Monitor Schedules/Visits of Patients according to Protocol, File and Collate trial documentation and reports, Archive study documentation and correspondence, Preparing Final Reports, and detailed Follow up letters after Monitoring Visits.• Training of the Clinical Trial site staff regarding Protocol, Investigational Product Management, Case Report Form filling and Good Documentation Practice. Show less

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  Iqvia asia pacific

  Apr 2021 - now

  • Senior Clinical Research Associate 2

    Oct 2024 - now

  • Senior Clinical Research Associate 1

    Apr 2022 - Sept 2024

  • Clinical Research Associate 2

    Apr 2021 - Mar 2022