JOB OVERVIEW

Responsible for performing a variety of routine testing procedures to obtain data for use in clinical trials research.

RESPONSIBILITIES

• Performs routine analysis of specimens and documents results in accordance with SOPs and applicable regulatory guidelines.
• Evaluates validity of analytical results against the algorithms displayed by the lab computer system.
• Identifies and documents potential performance errors or otherwise unusual results and escalate to senior lab personnel.
• Responsible for preparation of buffers and solutions for analysis, as required.
• May perform secondary review of analytical results when signed-off as competent to do so for applicable instrument(s) and/or data type(s).
• Responsible for post analysis sample and reagent storage.
• Assists in the development and writing of new laboratory procedures and techniques.
• Assists in good housekeeping of the lab environment, consistent with 6S standards.
• Notifies appropriate staff of supply shortages.
• Responsible for clear, accurate, and timely communications with cross functional stakeholders.
• Participates in continuing education through self-study, attending in-services and lectures and meetings.
• Supports safety, quality, and 6S requirements and initiatives.
• Complies with company's procedures and applicable regulatory requirements.

MINIMUM EDUCATION REQUIRED AND EXPERIENCE

• High School Diploma or equivalent required or Bachelor's Degree
• Some CAP/CLIA lab locations may require a BS in chemistry, biology, or medical laboratory technology degree
• 6 months relevant lab experience required or equivalent combination of education, training and experience required

REQUIRED KNOWLEDGE, SKILLS, AND ABILITIES

• Basic knowledge of lab principles.
• Basic knowledge of Good Laboratory Practices (GLP) and applicable regulatory agency standards.
• Knowledge of laboratory safety and infection control procedures and practices including standard precautions and hazardous chemical handling.
• Knowledge of laboratory equipment, instrumentation and terminology used in the area of responsibility.
• Basic computer skills.
• Ability to maintain effective reporting procedures and control workflow.
• Ability to effectively collaborate with internal stakeholders.
• Applicable certifications and licenses as required by country, state, and/or other regulatory bodies. 

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. https://www.q2labsolutions.com/careers

We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/q2-solutions-eoe

As the COVID-19 virus continues to evolve, Q² Solutions' ability to operate and provide certain services to customers and partners necessitates Q² Solutions and its employees meet specific requirements regarding vaccination status. https://jobs.iqvia.com/q2-solutions-covid-19-vaccine-status