Jon Cox Email & Phone Number

Greater Salt Lake City, Utah

Greater Salt Lake City Area

Greater Salt Lake City Area

• Prepare, advise, develop and cost proposals, ensuring accuracy and timely delivery• Responsible for the technical and regulatory accuracy of proposals generated and the intended clinical use of the test article being quoted.• Collaborate with subject matter experts/operational management on costing & design of laboratory proposals• Collaborate with Strategic Partnering Directors to communicate relevant Client information for those key accounts in their respective region• Work closely with Account Specialists, Account Managers and the Area Sales Directors to achieve regional sales targets • Provide technical direction to Associates in the sales and marketing team and within the NAMSA organization

Greater Salt Lake City Area

Monitored the initiation and performance of clinical trials at external research sites to assure compliance with all study procedures and regulatory requirements. Served as the primary liaison with research sites, tracked the progress of the study and resolved issues with study execution. Conducted site qualification, site initiation, interim monitoring, and study termination visits. Assisted in the development of study protocols, case report forms, and identifying potential research sites. Managed Phase I and II clinical trials, including overseeing CROs operations, guiding the efforts of other CRAs, and negotiating budgets.

Volunteer manager of $1.5 – 2 million in annual donations. Oversaw operating budget of $15,000-20,000. Reconciled books, cut checks, filed reports, and attended financial audits. Purchased materials and managed budgets for seven divisions. Supervised two clerks, who assisted maintaining financial records and membership database. Kept minutes of weekly meetings.

Clinical Research Associate for a prostate oncology drug trial. Initiated sites; reviewed clinical data and reports; confirmed subject eligibility; monitored site progress and adherence to study protocol; oversaw study drug shipment to sites; draft reports and correspondence to study sponsor and individual study sites.

Monitored clinical oncology drug trial at the Huntsman Cancer Institute (HCI), audited case report forms, prepared monitor reports, and reviewed findings with site. Interacted with physicians, pharmacists, consultants and HCI staff, assuring study was conducted according to the study protocol. Reviewed screening criteria and medical records to confirm eligibility of new study participants. Drafted annual report to the FDA, submitted adverse event reports to the FDA and IRB, attended Investigator Meetings. Coordinated shipments of experimental drug from China to the HCI, accounted for drugs given to study participants, and oversaw disposal of excess drug at end of study. Project manager for the collection of data, dataset review, resolution of data queries, and database entry of the phase one clinical trial data into a SAS database. Trained and supervised the database entry team members. Drafted budgets and interacted with contract companies.

Assisted physician in patient care, took patient histories, and scheduled physician’s appointments. Redesigned office documents for greater efficiency; revised filing system; filed claims with insurance companies; received and recorded payments; and performed minor bookkeeping and accounting.

Ensured completion of medical records in accordance with JACHO and Primary Children's Hospital standards. Interacted with medical staff, hospital administration, various hospital departments, and state agencies in fulfillment of the described duties. Audited patient billing statements, authorized reimbursements, and corresponded with patients and hospital administration. Reviewed pre- and post-discharge medical records for compliance with stated regulations. Participated on a number of CQI committees.

Drafted and coordinated correspondence with the office’s three networks; maintained computer and paper files for these constituencies; organized five major conferences each year; scheduled speaking appointments for various U.S. and international officials; oversaw office’s computer and supply needs; managed the organization’s intern program; supervised office’s interns; and prepared grant proposals and reports.

Coordinated events dealing with education restructuring and workforce quality initiatives; drafted correspondence with executives attending these meetings; arranged event speakers and venues.

Programmed the local and national itineraries for participants in the U.S. Information Agency's International Visitor Program; coordinated visitors' itineraries with local organizations, escort-interpreters, and U.S. Information Agency officials; proposed and maintained budgets for individual visitors and special projects.

Masters Of Business Administration

Education record

Activities and Societies: Family Practice Student Association

Bachelor Of Arts, Political Science

Activities and Societies: Member of Phi Kappa Phi, Pi Sigma Alpha, and Golden Key Honor Societies Four-month internship in Washington.