Manage day to day efforts and coordinate calendar of assigned team to ensure adequate pre and post sales support for designated products. Assist in setting of priorities where needed, based on business drivers. Learn the MACSima training process and support process to ensure the success of select priority customers with installation training and follow up support Work wit

With direct oversight, the Clinical Authorization Specialist Manages approval process for clinically complex cases Discusses complex medical necessity cases in all aspects of the prior authorization work (on label drug, off label drug, laboratory testing, and others as assigned) with attending physicians. Understands clinically complex medical situations and communicates

MIT Lincoln Laboratory seeks a highly motivated, detail oriented, curious and driven physicist, applied physicist, or researcher in a related field with hands on lab experience. The successful candidate will join a close knit, dynamic team pushing the forefront of quantum information processing and precision time keeping using trapped ions. As an active participant in cut

Research Scientist Analytical Instrumentation Req. # 20203 Company Name Waters Division Category Research and Development Location US MA Cambridge Type Regular Full Time Overview Come and join our diverse research team in the heart of Cambridge and help us in this new era of innovation! Participate in collaborations across departments, sites and more broadly with the scie

Please note, the functions below are representative of major duties that are typically associated with these positions. Specific responsibilities may vary based upon departmental needs. Similarly, not all duties that have been outlined will be assigned to each position. Collects & organizes patient data Maintains records and databases Uses software programs to generate gr

Per the direction of the section supervisor, performs a limited variety of laboratory procedures utilizing independent judgment and maintaining responsibility for assigned duties. Must be familiar with laboratory procedures in Micro. Must be computer literate. Must also be familiar with specimen processing protocols for both inpatient and outpatient procedures. May be req

` Town of Lexington Employment Opportunity We are currently accepting applications for the full time seasonal positions of Conservation Land Field Crew We anticipate hiring up to three full time seasonal positions Up to 29 hours per week from mid May to September; start and end dates are flexible Starting range for Crew positions $16.00/hr $18.00/hr based on experience No

Skillfully performs the job of drawing all types of blood specimens (with the exception of blood gases), from adults, children, and infants. The Laboratory Assistant is also responsible for a variety of clerical and record keeping duties, as well as specimen handling, shipping, ordering, EKG's and Holter's. Essential Job Duties and Responsibilities Specimen Handling Colle

As a temporary Laboratory Assistant in the Microbiology department at IDEXX, you will be assisting with some of the many tasks vital to the running of our network of Reference Labs. We receive thousands of clinical samples (blood, urine, fecal samples) every day from Veterinary Clinics, and we run tests on those samples to help veterinarians identify what might be wrong w

Co design and implement a target tractability system for oligo guided therapeutic mechanisms such as RNA degradation/interference, and up/down modulation of alternative splicing, poly adenylation, A> I editing, etc. Co develop a target/complex engagement model that combines target sequence, secondary+ tertiary structure, and oligo chemistry to drive binding assay designs

Associate Research Scientist Job Location Other Remote Office ID 2024 11150 Status Part Time Benefit Eligible Shift Varied Schedule Mon Fri Hours of Work varied Responsibilities The Associate Research Scientist will work collaboratively with HBFF Research Scientists to assist in the execution of high quality applied research projects, clinical research studies, evaluation

Perform routine environmental monitoring of the manufacturing facility. Perform routine sampling and testing of the utility systems. Perform Manufacturing Process Monitoring Perform QC sample receipt and aliquoting as necessary. Complete documentation in accordance with current Good Manufacturing Practices (cGMP) ensuring data integrity. Maintain QC Micro related systems

Provide scientific and medical contribution to the design and execution of clinical trials Collaborate on, or lead where appropriate, the preparation of clinical study related documents including protocols, clinical study manuals, ICFs, charters, statistical summary reports, meeting presentations, publications, and clinical sections of regulatory documents Engage with inv

Responsible for the performing of tests and/or calibrations and evaluations or results related to GMP, ISO and non GMP materials and products as appropriate Follow documented procedures and document test data as required Utilize the following techniques to characterize organic and inorganic chemicals FT NMR, GC/MS, GC, HPLC, FT IR and wet chemistry tests Write test proced

If you are wondering what makes TRIMEDX different, it's that all of our associates share in a common purpose of serving clients, patients, communities, and each other with equal measures of care and performance. Everyone is focused on serving the customer and we do that by collaborating and supporting each other Associates look forward to coming to work each day Every ass