• Conducted site qualification, initiation, interim monitoring, and study closeout visits.• Ensured safety and protection of study subjects through compliance with the study monitoring plan, AbbVie SOPs, ICH Guidelines, and applicable regulations.• Monitored activities conducted by clinical investigative sites to ensure successful execution of the protocol.• Trained site staff on therapeutic areas, protocol requirements, proper source documentation, and timely EDC completion.• Assisted fellow CRAs as an eTMF subject matter expert by answering questions, conducting training, holding office hours, and presenting monthly reports to management.

• Conducted site qualification, initiation, interim monitoring, and study closeout visits for Phase 1-4 studies.• Ensured safety and protection of study subjects through compliance with the study monitoring plan, AbbVie SOPs, ICH Guidelines, and applicable regulations.• Monitored activities conducted by clinical investigative sites to ensure successful execution of the protocol.• Trained site staff on therapeutic areas, protocol requirements, proper source documentation, and timely EDC completion.• Assisted fellow CRAs as an eTMF subject matter expert by answering questions, conducting training, and presenting monthly reports to management.

• Screened and obtained informed consent from potential subjects using the protocol’s inclusion/exclusion criteria• Collected patient vitals and specimens and shipped them to the central laboratory adhering to IATA standards• Preformed EKGs, spirometry (PFTs), and capillary puncture tests• Maintained effective and ongoing communication with sponsors, CRAs, IRBs, research participants, and the primary investigator• Prepared and maintained study materials and regulatory documents for site initiation visits, interim monitoring visits, and study closeouts• Created source documents and CRF templates based on individual study protocols• Ensured accuracy of eCRFs in sponsor specific online portals through data verification and query management• Trained new Clinical Research Coordinators and study staff on protocol procedures

• Greeted patients and visitors and directed/escorted them to their destinations• Assisted patients with their non-medical needs and provided support services for staff• Performed clerical support including answering phones and filing medical documents

• Ensured the health, safety, and protection of patrons• Enforced the rules and regulations of the public pool• Rescued swimmers in distress and provided First Aid• Treated injuries, sudden illnesses, and other medical emergencies

• Screened potential subjects using the protocol’s inclusion/exclusion criteria• Obtained informed consent from study participants and increased enrollment• Collected and monitored patients’ vitals and weekly lab results to compare effectiveness of study medication and ensure patient safety• Managed clinical trial site independently through communication with the study sponsor, time management, and product accountability

• Scanned case studies for genetic and phenotypic information relating to a rare genetic kidney disease (FJHN)• Compiled and analyzed characteristics of the disease using Survival Analysis• Discovered correlations between genetic factors and age of kidney failure in FJHN patients• Presented research findings at scientific meetings• Assisted research fellows by performing data entry and analysis of dialysis patients’ treatments

• Conducted interviews with residents in assigned areas by following stringent guidelines and confidentiality laws • Explained the purpose of the census and answered residents' questions in different languages• Recorded and verified data from selected addresses on questionnaire forms