Iqra Choudhry, MPH

• Reviewed the protocol, Informed Consent Form, and follow-up procedures in detail with potential study subjects as well as Clinical Research Coordinators on site. • Partnered with global and local CRO and Sponsor teams to provide high level country strategy and actively drive study progress and local/country level study delivery • Accountable for site-level goal setting and study-specific deliverables within the clinical sites • Regularly communicated with central and local ethics board representatives, IRB, and maintained trial regulatory documents on-site. • Routinely involved in study/protocol activation processes and submission of regulatory documents to ethics board through WCG, Advara etc • Ensured adherence to protocol requirements, scheduled subjects for follow-up visits, and managed distribution and documentation of investigational, background, and rescue medications in accordance with regulatory guidelines • Responsible for training new coordinators in trial activities, ensuring PIs and Sub-Is are all up-to-date in their trial training, and mentoring clinic volunteers in clinical research • Experience with preparing for and taking the lead at SIVs, SQVs, SMVs, SMCs, and completing site feasibility questionnaires at the discretion of the Principal Investigator

• Planned, implemented and coordinated all aspects of data collection and source documentation, as per ICH/GCP guidelines and study protocols. • Experience conducting spirometry, ECG, FeNO, PEF measurements, phlebotomy, biological sample processing and shipping, and actigraphy • Extensively familiar with conducting data entry via RAVE, ERT, IXRS/IWRS, IQVIA,Covance, Q2 Solutions, Eurofins, InForm, Cenduit, EndPoint, Signant Health, DrugDev, WCG, SAFRNS, TrialManager, and more • Ensured peers delivered accurate data entry through quality control and monitoring. • Organized Regulatory Documents through IRB and updated accordingly and in a timely manner. • Liaised with relevant study sponsors, external monitors and all investigators; providing logistical support to other initiatives and events as well as basic lab support, as needed

• Communicated effectively with staff, patients and insurance companies by email, telephone and paperwork. • Utilized ZOHO and Accuro EMR to manage and confirm patient data, such as insurance, demographic and medical history information. • Researched and compiled statistical data to support cost control and care improvement initiatives. • Examined, interviewed and measured patients in order to determine orthotics and compression stocking needs and identify factors affecting appliance fit.

The removal of the Ara h 1 allergen from the common peanut (Arachis hypogaea) genome using CRISPR-Cas9.

Study was done to verify the effects of laser therapy performed with Ga-Al-As Diode Lasers (780 nm, 2500 mW) on human cartilage cells in vitro.