Jalyn Thompson Email and Phone Number

Assists in developing materials and tools to train study participants on protocol requirements, research plans, and visit schedules Records and manages data collected from participants during and after their visits Ensures the study complies with regulations from medical facilities and pharmaceutical companies. Maintain ISF documents.Supports and coordinates activities related to the clinical trial Communicates with participants about the study's objectives and administers questionnaires Manage the collection, labeling, storage, and transport of specimens Ensures all equipment are calibrated in the required time allowed and supplies needed for the study are in stock and working properly.Maintains research records, including case report forms, drug dispensation records, and other regulatory forms Ensures that I'm up to date on all trainings and help educate and mentor clinical staff, research team, and other coordinators Schedules patients, documents trial progress, and performs data entry Work with principal investigators (PIs) and Sub-Is to determine if the study is viable.

- Communicate the customer requirements of existing and new projects to new hires and management. - Coordinate and conduct interviews for various positions ranging from entry level to management.- Hire, train, and conduct staff members and new hire orientation for temporary and full-time employees.- Perform payroll administrative duties such as payroll setup, entry, and approval.- Investigate grievances and training issues while providing solutions and alternatives that meet the needs of business.- Coordinate and administer transfers, promotions, disciplinary actions and terminations.- Create and manage daily reports while communicating updates and adjustments to management and customers - Manage and run operations of different shifts and ensure that any rotating shifts are staffed, trained, and certified

- Traveled up to 80% regionally and nationally to monitor and audit various projects: Areas of projects worked: Hematology Oncology – Glioblastoma (III)(MV), Lung (II, III)(MV,COV), Breast(I,II,III), Multiple Myeloma (II, III) - Maintained timely and effective communication with management, team members and site staff. Routinely anticipated/identified potential issues and implements corrective actions while keeping project leadership apprised of team issues, seeking guidance as needed. - Provided direction and training for other CRAs assigned to a project or study as well as co-monitor with them. - Regulatory Documentation - Assured compliance within local regulations, CFR/ International Conference of Harmonization (ICH) and GCP guidelines, and Company and Sponsor SOPs. - Responsible for site management and site staff performance including: monitored all types of clinical trials; participated in all types of site visits; assured compliance with all protocol requirements; assured effective patient identification and recruitment plan is in place- Assured timely reporting of Adverse Events (AEs)/Serious Adverse Events (SAEs) and protocol violations; ensures proper storage, dispensation, and accountability of all Investigational Product(s) and trial-related materials- Data Handling - Performed source data verification according to contractual requirements.

- Analyzed, planned and coordinated the development of each individual claim in advance, implemented the plan expeditiously to meet deadlines. This required an extensive collection of medical and vocational work reports accumulated through contact with many sources.- Consulted physicians to obtain and discuss medical facts, findings, and inferences so that a correct, final decision may be made on disability claims.- Evaluated and judged medical information regarding a claimant’s mental and/or physical residual functional capacity through utilization of extensive knowledge of anatomy and physiology.- Requested authorization for very large amounts of tax monies for various medical examinations, specific laboratory tests, x-ray procedures, etc., on a daily basis.- Conducted conferences with claimants and/or other representatives to explain the technical reasons for denial of benefits.- Interfaced with other professionals to explain the SSA (Social Security Administration) regulations utilizing technical knowledge.