Job Overview Perform routine analysis of patient specimens according to standard operating procedures (SOPs). Evaluate specimen acceptability upon receipt and during the review of analysis results. Evaluate validity of specimen results against the algorithms displayed by the lab computer system. Document all corrective actions taken. May perform secondary review of patient results when signed-off as competent to do so for applicable instrument(s) and/or data type(s). Responsibilities Maintain quality control of all laboratory testing to ensure accurate and timely lab reporting. Perform pending workload review periodically during the day; find pending assays and resolve outstanding work prior to the completion of testing for the day. Assist in the development and writing of new medical laboratory procedures and techniques. Follow safety procedures as per laboratory SOPs. Notify appropriate staff of supply shortages. Participate in continuing education through self-study, attending in-services and off-site lectures and meetings. Minimum required education and experience Bachelor's Degree in a Science Discipline Equivalent combination of education, training and experience Applicable certifications and licenses as required by country, state, and/or other regulatory bodies Required knowledge, skills and abilities Ability to follow verbally communicated or written procedures Experience in routine laboratory procedures Attention to detail when performing laboratory procedures Ability to develop clear and efficient experimental documentation Ability to establish and maintain effective working relationships with coworkers, managers and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $24,400.00 - $50,900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
