Responsibilities- Implemented coordinate daily clinical trial activity provides guidance on administration; compliance, financial and other related aspects of clinical studies, Train and mentor new study personnel. Skilled in medical laboratory and clinical procedures, tactful communicator, adept at prioritizing managing tasks and meeting all deadlines, Support and assist the Principal Investigator in conducting and managing clinical trials.

~Coordinate, manage clinical trials start to finish. ~Assure prompt accurate data flow to Pharmaceutical Sponsor. ~Participate inform process with PI, obtains appropriate signatures, dates, on forms. ~Reviews, comprehends protocol. ~Attends investigator meetings. ~Implement recruitment strategies, accordance with IRB requirement approvals. ~Screen subjects eligibility using protocol specific inclusion/exclusion criteria, review patient clinic Charts, medical records. ~Collects data required per protocol, maintains study timelines. ~Proficient data entries; web-based source documentation. ~Experienced all laboratory procedures, 18 years Hospital/Clinical laboratory experience, IATA certified 2015, Phlebotomist certified. ~Proficient EKG's, 24 hr. Holter monitoring, Master-scope Spirometry. ~Coordinates, Facilitates monitoring visits, assist PI promptly reporting unanticipated problems, Involving risks to research participants. ~Maintains accurate records, study drug dispensing/return, drug storage, lab supplies, ~Keeps daily temperature logs. ~Obtain; vital sign, study specific assessments per protocol. ~Proficient computer skills, micro-soft office, word, ms-outlook, excel.

Advanced Histology Dept; organized, accessioning, processing surgical specimens, Pathological examination, performed MOHS frozen process; cut, stain for path exam

specimen processing, equipment calibrations,Worked other departments; chemistry, urinalysis, and bacteriology.

~Support, Coordinate, and facilitate daily clinical trial activities, with Principal investigator. ~Guidance on administration compliance, financial, protocol Requirements; training study specific, conducts, and participates with informed consent process, including answering any questions related to the protocol, obtains appropriate signature, dates on forms. ~Assures that amended consent forms are appropriately implemented and signed. ~Attends investigator meetings, prepares study materials Include; but not limited to; the informed consent document, case report forms, enrollment logs. ~Establishes organize study files, source documentation, screen subject for eligibility using protocol specific inclusion/exclusion criteria, documenting each potential participant's eligibility applying to a data base excel program, coordinates participants tests and procedures required by sponsor, collects data required per protocol. ~Assures timely completion of case report forms, maintains study timelines. ~Maintains accurate inventory of study supplies, device accountability logs, adhere to protocol requirements.