Project Manager Quality Control
Resume:
Eric K. Murphy Contact Information:
High Point, NC 27265
Phone: 336-***-**** (home)
336-***-**** (mobile)
Email: ******@***.***
Medical Technologist/ Microbiologist/ Laboratory Professional with proven experience in the Clinical Laboratory. Successfully achieved value-added results in the area of Microbiology. Over 15 years of Microbiology experience within a hospital and reference lab setting.
Solstas Lab Partners (formerly Carillion-Spectrum)
Microbiology Supervisor/ Medical Technologist (Department of Microbiology)
October 2010 to Present – Full-time
• Implemented compliance procedures and regulations within the Department of Microbiology
• Identified aerobic and anaerobic bacteria by using various bio-chemicals and selective media; performed
various serological tests accurately with attention to detail.
• Review and report clinical laboratory data (i.e. electronic batch records) accurately with proficiency
Duke University Medical Center
Technologist II (Department of Microbiology – Chlamydia - STD Lab)
October 2010 to Present – Part-time/Casual
June 2009 to September 2010 – Full-time
April 2005 to May 2009 – Part-time/Casual
• Implemented compliance of various quality control procedures as indicated by standard operating procedures.
• Test for Chlamydia trachomatis and Neisseria gonorrhoeae by PCR and Tissue Culture
• Review and report clinical laboratory data (i.e. electronic batch records) accurately with proficiency
INC Research (A Full Service Contract Research Organization – Clinical Trials)
Quality Assurance Auditor
March 2008 to May 2009 – Full-time
• Wrote and issued inspection reports in accordance with standard Company formats and timelines, ensuring clear communication of audit findings to the relevant project team members and/ or functional area management.
• Reviewed responses to audit findings for appropriateness and completeness while maintaining documentation of auditing activities.
• Hosted Trial Master File audits and Sponsor’s Qualification Audits; involves the preparation and responsibility of audit schedules, audit agendas, facility tours, team meetings, teleconferencing, and meeting minutes
Esoterix Clinical Trial Services (A LabCorp Company)
Project Manager
September 2006 to February 2008 – Full-time
• Trained in the application of GLP / GCP / GMP / ICH regulations for the quality compliance of standard operating procedures (SOPs) and protocols.
• Reviewed study protocols (Phase I-IV) and standard operating procedures to implement specifications in the compliance of GLP/ GCP.
• Managed the setup of all the clinical laboratory testing for a FDA regulated central lab for over 25 clinical trial protocols (Phase I-IV). This would include pharmaceutical companies, contract research organizations (CRO) and investigator initiated studies.
Laboratory Corporation of America
Supervisor/ Team Leader/ Microbiologist (Microbiology)
July 1999 to August 2006 – Full-time
January 1998 to June 1999 – Part-time
• Managed technologists within the LabCorp organization for 7 years in the department of routine Microbiology and Clinical Trial Projects.
• Ensured compliance of all regulations and Quality Assurance procedures within the Department of Microbiology (FDA regulated laboratory)
• Motivated individuals in meeting deadlines and goals for the company.
• Implemented performance management systems designed to connect individual performance with the attainment of corporate goals and initiatives.
• Trained in Good Laboratory Practice/ Good Clinical Practice (GLP/ GCP) as it relates to the laboratory procedures.
• Routinely administered Quality Control programs with regards to the testing of samples.
• Implemented Quality Control procedures during the daily testing of patient samples.
• Performed environmental sampling of aseptic areas, personnel and utility systems
• Evaluated environmental date for adverse trends
Veteran Affairs Medical Center
Microbiologist - Medical Technologist (Microbiology and Serology)
January 1998 to June 1999 – Full-time
• Identified aerobic and anaerobic bacteria by using various bio-chemicals and selective media; performed various serological tests accurately with attention to detail.
• Listed and rationalized the requirements for the management of samples from the time of collection.
• Implemented daily Quality Control procedures in compliance of SOP.
Laboratory Corporation of America
Microbiologist - Medical Technologist (Microbiology)
July 1996 to December 1998 – Full-time
• Identified aerobic and anaerobic bacteria by using various bio-chemicals and selective media.
• Listed and rationalized the requirements for handling of specimens from the time of collection.
• Performed various tests accurately with attention to detail. Various testing methods include: Enzyme Immunoassay (EIA), Gas Liquid Chromatography (GLC), Minimum Inhibitory Concentration (MIC), Genprobe, Environmental Testing (i.e. A-test and Millipore) and Cell culture.
• Masters in Business Administration (MBA) 2005
Averett University, Danville, VA
• Bachelor of Science in Medical Technology (Clinical Laboratory Science) 1996
East Carolina University, Greenville, NC
• Other Skills: Computer Software experience includes Microsoft Office: Word, Excel, Access, and PowerPoint
• Bayer Investigator Meeting/ “New Orleans”: Power-point presentation on the role and capabilities of the Central Lab (Esoterix/ LabCorp); March 5 – 7, 2008
• Bayer Investigator Meeting/ “New York”: Power-point presentation on role and capabilities of the Central Lab (Esoterix/ LabCorp); January 28, 2008
• Certification: Medical Technologist #202732/ American Society of Clinical P
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