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Muhamad Khizar Hayat
Clinical Research Associate
Lahore,Non-US
Summary
Analytical Clinical Research Associate with talents in project development and screening to document and report clinical study progress. Coordinates and facilitate research activities and submits protocols for regulatory approval. Serves as point-of-contact for clinical research professionals and coordinates lab samples to compile detailed data. Organized and dependable candidate successful at managing multiple priorities with a positive attitude. Willingness to take on added responsibilities to meet team goals.
Overview
2
2
years of professional experience
Work History
Clinical Research Associate and Clinical Data Manager
Tigermed Group
02.2021 - Current
- Responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical studies in accordance with Tigermed or sponsor StandardOperating Procedures (SOPs), International Conference of Harmonization Good Clinical Practice standard (ICH-GCP), ClinicalPractice standard (GCP) and other applicable regulations .
- The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget .
- Be guided to electronic and Clinical data review for the data in database against CRFs
- Develop positive communication channel with team and customers
- Be guided to assist in database QC
- Conduct medical coding for Adverse Event, Medical History,Concomitant Medication, etc
- Issue and resolve data queries related to medical coding.
Quality Assurance Officer
High noon Laboratories Limited
05.2020 - 01.2021
- Assure the quality of product according to GMP guidelines and SOPs of Highnoon laboratories limited.
- Responsible for finding out areas where errors prevail, minutely observing every activity and the drugs being manufactured or packed for visible defects.
- Responsible for assuring ongoing compliance with quality and industry regulatory requirements
Education
Bachelors - Science
Lahore Pharmacy College Pharmaceutical
01.2020 - 01.2001
Intermediate - undefined
Punjab Groups of College Science
10.2013 - 09.2014
Skills
Time Management
Accomplishments
- Designing and conducting effective long term follow up studies (ICON)
- FY 2021 Generic Drug Science and Research Initiatives (FDA)
- Centralize, Track and Empower data review GCP (PerkinElmer)
- Good Clinical Practice (NIDA & GCP finding)
- Modernizing Neuroscience Clinical Trials Using a Virtual Framework A Perspective on Endpoint
- Measurement and Best Practices (ICON)
- Elevating the Site-Sponsor Experience: Learning Management SaaS in Clinical Trials (IQVIA)
- Covid 19 Phase III CRA: Source Data Verification
- Covid 19 Phase lll CRA: Site selection, SSV Report, EC submission,SIV, Enrollment, Biological Sample shipment, TMFdocuments
- Covid 19 Phase lll CRA: Site selection, SSV Report, EC submission,TMF documents
- Covid 19 Phase III CRA: Site selection, SSV Report, EC submission,TMF documents
- Covid 19 Phase III DM: Manual Data Review and Medical Coding(WHO and MeDRA Coding)
- Covid 19 Phase III DM: Manual Data Review
- Covid 19 Phase III DM: WHO Medical Coding
Interests
Work Availability
monday
tuesday
wednesday
thursday
friday
saturday
sunday
morning
afternoon
evening
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Timeline
Clinical Research Associate and Clinical Data Manager
Tigermed Group
02.2021 - Current
Quality Assurance Officer
High noon Laboratories Limited
05.2020 - 01.2021
Bachelors - Science
Lahore Pharmacy College Pharmaceutical
01.2020 - 01.2001
Intermediate - undefined
Punjab Groups of College Science
10.2013 - 09.2014
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