David Ealy Email & Phone Number

Madison, Wi, Us

Madison, Wi, Us

Champaign, Illinois, Us

Securities offered through Cetera Advisor Networks LLC, member FINRA/SIPC, a broker/dealer. Advisory Services offered through Cetera Investment Advisers LLC, a registered investment advisor. Cetera is under separate ownership from any other named entity. 3 FREMONT CIRCLE, MADISON, WI 53704

Burlington, North Carolina, Us

Provides administrative and scientific support for toxicology studies, including prestudy tasks e.g., protocol development, costing, scheduling, monitoring the inlife progress of assigned studies, interacting with clients, and/or reporting (including peer reviews). Drafts and finalizes protocols and amendments, including incorporation of client comments and quality assurance review remark. Also draft reports, incorporates contributions, submits and addresses quality assurance inspection items on Good Laboratory Practices regulated studies, finalizes reports, completes report amendment, and prepares tabulated summaries. Responsible for reviewing data and identifying and resolving deficiencies, compiling data for clients for regular study progress updates, hosting client visits, and assisting in regulatory visits as appropriate. Identifies opportunities for process improvements, takes ownership of processes, drives process improvement to completion, and participates on other process improvement teams

Burlington, North Carolina, Us

Responsible for facilitating rapid proposal development within mammalian toxicology by acting as the point of contact and generator of non-standard responses. Served as the principal liaison between Toxicology and Client Services/Business Development at Proposal Status meetings. Prepared documents that meet tight turnaround times demanded by internal clients and monitors correspondence, including toxfile and telefax traffic, to anticipate incoming requests. Also assisted with initial development of draft protocols, protocol outlines, or other related information to assist in the costing process for standard inquiries.

Princeton, New Jersey, Us

Responsible for providing administrative and scientific support to Study Directors, with the assistance from senior staff. Responsibilities included writing Protocols and Amendments and ensuring compliance with appropriate standard operating procedures, Good Laboratory Practices, and regulatory agency guidelines. Initiated costings, scheduled studies, and monitored the inlife portions of studies. Also assisted Study Directors with proposal management and provided technical/scientific guidance and leadership to ensure accurate project completion. Involved in Client visits, met with Clients to discuss study progress, and participated in study meetings.

Princeton, New Jersey, Us

Responsible for conducting technical phases of infusion specialty studies, including study management, Client communication, and quality check procedures in compliance with appropriate Standard Operating Procedures, Good Laboratory Practices, and regulatory agency guidelines. Prepared costings, staff plans, and scheduling activities; assisted in the development of new procedures and Standard Operating Procedures; and helped to train new and less experienced staff.

Princeton, New Jersey, Us

Responsible for collecting, documenting, and managing pertinent data, including animal observations, test material administration, and clinical sample collection to ensure compliance with appropriate Standard Operating Procedures, Good Laboratory Practices, and regulatory agency guidelines. Monitored animal health and welfare in compliance with the Animal Welfare Act and also responsible for compliance with the Association for Assessment and Accreditation of Laboratory Animal Care International standards. Responsible for independently carrying out technical parts of most toxicology studies, which included study management, data organization, responding to quality assurance audits, using communication skills with internal and external Clients, and performing quality check procedures. Performed advanced dosing and clinical sampling techniques, reviewed his own and others’ data, and identified potential problems. Trained, assisted, and instructed less experienced staff. Assisted in Client tours or Client interaction during study initiation.

Master'S Degree, Biotechnology

Bachelor Of Science (B.S.), Integrative Biology And Chemistry

Education record

Education record