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.

 
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 required.

MINIMUM REQUIRED EDUCATION 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 required.
• 6 months relevant lab experience required Or
• Equivalent combination of education, training and experience required.

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