Scientist I / Medical Technolgist I - Hematology

Work Schedule Other Environmental Conditions Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description This is a fully onsite role based at our Global Central Laboratory in Highland Heights, KY. We welcome applicants from all locations within the US. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate.  Must be legally authorized to work in the United States without sponsorship. Must be able to pass a comprehensive background check, which includes a drug screening. This will be located on-site in Highland Heights, KY 2nd Shift: Tuesday-Saturday from 12-8:30 PM ET *Shift differentials provided* At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic experts. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations. The Scientist I or Medical Technologist I (If certified) performs analysis and evaluates individual and related laboratory data, recognizes patterns or trends that suggest significance of results and determines the level of clinical significance. Evaluates individual and related laboratory data to recognize patterns or trends that suggest significance of results. Assists in authoring and modifying SOPs (standard operating procedures). We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. What You'll Do: • Supports the Hematology Group • Perform, review, and interpret complex, esoteric, and routine chemical, hematological, coagulation, renal, lipid, and hormonal analyses by manual, automated, and/or microscopic methods. • Integrate analytical results with specific and varied clinical trial protocols to evaluate the credibility, appropriateness, and accuracy of test results in order to facilitate the inclusion or exclusion of subjects from research programs. • Operate, maintain, troubleshoot, and repair clinical laboratory equipment, including performing routine preventative maintenance, calibrations, and safety checks. Recognize and resolve instrument problems, independently evaluating and taking appropriate action to ensure accurate patient data when major instrument issues occur. • Evaluate analytical reagents, calibrators, and QC standards to ensure the accuracy of analytical results. • Evaluate quality control procedures and results, and implement corrective actions when indicated. Perform ongoing statistical data analysis to detect trends or problems and undertake corrective action. • Conduct comparison studies for precision, accuracy, and linearity on new or existing assays or instruments. Assist in the design and implementation of new procedures and in the modification of existing methods. • Provide instruction for new employees and students in the theory and practice of laboratory medicine and the interpretation of