Tisha Williams Email & Phone Number

Hayward, Ca, Us

Quality Lab Technician (licensed phlebotomist): • Performed daily LDX cassette testing using Fingerstick, whole blood and serum test samples for QC final release testing for Cholestech’s product disposition. • Dual responsibility in Phlebotomy for recruiting and scheduling donors when Phlebotomy work is necessary. Maintained all QC laboratory inventory items such as laboratory supplies, donor money payment, and tracking donor blood volume via a database. • Perform basic laboratory tasks by performing daily verification of QC LDX bank optic checks, LDX data entry into a server database, temperature monitoring of cold room and freezers, and laboratory cleaning.• Acquired basic knowledge and understanding of GLP/GMP and FDA QSRs by weekly exams administered by the QC manager. • Solid knowledge and skills on the understanding of patient safety, donor confidentiality rules and bio-hazardous requirements with personal protection equipment.

Quality Lab Technician (licensed phlebotomist): • Performed daily LDX cassette testing using Fingerstick, whole blood and serum test samples for QC final release testing for Cholestech’s product disposition. • Dual responsibility in Phlebotomy for recruiting and scheduling donors when Phlebotomy work is necessary. Maintained all QC laboratory inventory items such as laboratory supplies, donor money payment, and tracking donor blood volume via a database. • Perform basic laboratory tasks by performing daily verification of QC LDX bank optic checks, LDX data entry into a server database, temperature monitoring of cold room and freezers, and laboratory cleaning.• Acquired basic knowledge and understanding of GLP/GMP and FDA QSRs by weekly exams administered by the QC manager. • Solid knowledge and skills on the understanding of patient safety, donor confidentiality rules and bio-hazardous requirements with personal protection equipment.

• Recruited patients for clinical trials; via newspaper, radio, phone and/or television in collaboration with CDM.• Positive Partners II for super-infection in HIV positive individuals and their significant other(s). • Participate in study team meeting(s) and presentations, as well as other CR&D-related meetings with limited supervision.• Responsible for AE/SAE reconciliation and writing IRB approvals. • Maintain a detailed log of regulatory materials; data entry, ordering supplies and keeping inventory.• Increased minority response to HIV (AIDS) awareness by 25% just in No. California (2007).Follow-up participants care and helping identify new medication(s) approved by FDA for HIV. Schedule and conducted visitation appointments; obtained patient medical history, vital signs, venipuncture, exam preparation. payment compensation and travel expenses.

• Coordinates recruitment of participants and develops information packets for the participants. • Monitors and tracks participants progress through-out the project and provides follow-up as needed. • Assisted with the development of research instruments and training of new research assistants. Edits and manipulates data; performs data manipulation to produce progress reports including basic statistical analyses. Maintaining project(s) records & reports, and reviewing regulatory literature relating to research project(s). • Conducted detail, and complex in-person and/or telephone interviews. Responsible for data quality assurance and general coordination of small scale research projects as well.• Calling IVRS for collection and dispensing of study drug(s).

As, Chemistry

Activities and Societies: Toast Masters

Economics