IQVIA Senior Laboratory Tech Specialist in Livingston, United Kingdom
Q2 Solutions is a leading clinical trial laboratory services organization with end-to-end laboratory services and secure, enterprise-wide biospecimen and consent management solutions. With a relentless focus on quality and innovation, Q2 Solutions uses its global experience and scientific expertise to transform science and data into actionable medical insights that help customers improve human health. A joint venture of IQVIA (formerly QuintilesIMS) and Quest Diagnostics, Q2 Solutions combines the best of each parent organization’s clinical trials laboratory services capabilities to fulfill its mission of treating each sample as if a life depends on it.
Act as a specialist for the laboratory technical systems (including NewLIMS/QLIMS) and provide technical guidance on the design of the clinical trial database in collaboration with Project Services, Global Laboratory Teams, Translational Science Laboratory, Scientific Review, Data Management, Quality Assurance, Global Database Operations and Information Technology teams as necessary.
Reviews laboratory testing and test code requirements for new studies, responds to technical inquiries and provides technical documents and data either directly or by maintaining study specific databases.
Attends internal study design meetings to discuss testing requirements, test code availability and highlight potential challenges.
Submits requests for new test codes or amended test codes via the TCWA system.
Monitors the Technical Services Database Change Request Service Now ticket system to perform test code loading into clinical trial database and the completion of Blood Volume Charts.
Monitors the Technical Services Query Service Now ticket system responding to inquiries from other departments requesting specific laboratory or testing information.
May draft new standard operating procedures (SOPs) and assist in the maintenance of existing SOPs related to the departmental activities.
Assist in Quality Assurance activities by aiding senior team members investigating quality incidents and developing CAPA plans.
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
Knowledge of clinical laboratory regulations, GxP and /or ICH guidelines
Knowledge of laboratory equipment, clinical laboratory assays.
Proficiency in PC applications such as word processing, spreadsheets, database management
Excellent attention to detail, organizational skills, verbal and written communication skills
Ability to work independently as well as in a team environment
Ability to establish and maintain effective working relationships with co-workers, managers and clients
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
Bachelor’s degree in life sciences or other relevant field and 1-year relevant clinical laboratory experience; or equivalent combination of education, training and experience
At IQVIA, we have a vision. Where every healthcare decision is based on evidence. Where data science and human science come together to improve global health. Where new and creative solutions aren’t just possible – they are expected.
Thank you for your interest in growing your career with us. It takes insight, curiosity, and intellectual courage to transform healthcare. The 56,000+ employees of the IQVIA family of companies, including Q2 Solutions, are reimagining a world without the consequences of disease. We are brave minds bringing powerful ideas to reality. At IQVIA, you can truly make an impact in an environment where you’re supported to succeed.
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