Taimur Malik

Experience

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  MOSES CONE MEMORIAL HOSPITAL

  Jun 2014 - Aug 2014

  Clinical Intern

  ● Treated patients from initial admission, through history taking and examination, until release.● Conducted daily morning and evening rounds under Dr. Suresh Nagapan, Head of Pediatrics● Presented on common genetic disorders in children to attending physicians during grand rounds.

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  Capital Digestive Care

  May 2016 - Nov 2020

  Medical Assistant & Hepatitis C Coordinator

  ● Assisted Drs. Birns, Gloger, Witten & Bhinder at their gastroenterology clinic● Collected patient histories and vitals, help patients with medications as well as deliver lab and imaging results● Assisted Hepatitis C patients manage their illness by counseling them in treatment options, risks and benefits of treatment● Aided patients in finding alternative options such as clinical studies or new medication in case of unsuccessful treatment

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  The GW Medical Faculty Associates

  Nov 2020 - Apr 2022

  Lead Clinical Research Coordinator

  ● Coordinate NIH/Federal as well as industry sponsored Phase II-IV clinical trials and grants from site initiation(SIV) to site close out.● Work with local and central IRBs to receive approval for prospective clinical trials.● Assist in contract and budget development for both federal and industry sponsored trials.● Develop SOPs and MOPs for grants and studies.● Recruit patients for trials from GWU MFA and Hospital and conduct necessary sample collections including blood draws.● Monitor patients for any adverse events and document as necessary.● Assist in creating trial protocols, informed consent forms, and conduct data and statistical analysis for grants.● Perform data monitoring and integrity checks and enter data into various EDC systems. Show less

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  AstraZeneca

  May 2022 - now

  Global Study Manager - Early Oncology

  Manage a pivotal global multi-arm, phase II, platform study for non-small cell lung cancer with over 90 sites in 12 countries.Provide oversight of all CRO activities conducted on the study including site start-up, data and sample management, Track sample shipments and sample data including blood and surgical samples.Lead development of study documents including informed consent forms, study plans, and patient facing materials.Oversee drug supply activities to ensure timely shipments of investigational products. Manage and oversee third party vendors including start-up, budgets, contracts, and data delivery.Review and raise queries for missing or incorrect information in electronic data capture systems (EDC) Guarantee study is in regulatory compliance by tracking trainings, trial master file metrics, and safety information distribution metrics. Show less