As a temporary Laboratory Assistant at IDEXX, you will assist with some of the many tasks vital to running 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 with someone's pet. In this role, you will be

As a temporary Laboratory Assistant 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 with someone's pet. In this role

As a temporary Laboratory Assistant 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 with someone's pet. In this role

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting opera

Accurately and quickly perform routine lab tasks, physical or chemical testing of finished goods, materials in process, or raw materials. Interprets these results with minimal supervision. Assists in developing new test methods, running non routine and new tests. Develops special customer tests and assesses new equipment by running trials. Performs routine calculations as

The Clinical Trial Assistant (CTA) will be responsible for a wide variety of matters in support of Pharming's growth as we increase the number of both pipeline and marketed products. Core functions include Set up, organize, and maintain clinical study documentation (e.g. Trial Master File documents, clinical study site documents, email correspondence, training materials,

The Clinical Laboratory Trainer Histology prepares and facilitates training for new hire and existing employee training in the clinical laboratory, with guided direction from operational and training leadership. This role supports the histology department through subject matter and training expertise to ensure all team members are trained properly and competencies are suc

Otsuka Pharmaceutical Company is a global healthcare company with the corporate philosophy "Otsuka people creating new products for better health worldwide." Otsuka is seeking an Associate Director/Director/Senior Director, Global Clinical Development (remote) responsible for the design and oversight of clinical research programs and protocols for OPDC products under good

Identification and validation of patient reported outcome measures (PROMs) and Clinical Outcome Assessments (COAs; i.e., patient reported outcome [PRO], clinician reported outcome [ClinRO}, observer reported outcome [ObsRO], performance outcome [PerfO], digital health technologies [TechRO]) as well as other patient centered outcomes (e.g., patient relevant biomarkers or v

Provides exceptional customer service to all consumers and members of the clinic staff Fills prescription orders and makes them available for verification under direct supervision of the registered pharmacist Orders, receives and stores incoming pharmacy supplies Receives and processes wholesaler medication orders Verifies medication stock and enters data in computer to m

Provide superior clinical consultation and clinical account management with a focus on client satisfaction, client retention, and trend management Collaborate with the client to establish achievable but aggressive clinical program goals, implementation and ongoing management of utilization management programs, improvement in medication adherence rates, improvements in the

Independently perform the following responsibilities under the direction of the Product Development Manager and/or Program Head to coordinate, manage, and lead the overall execution of clinical studies or group of clinical studies while following appropriate GCPs and SOPs Provide scientific insight into study design and disease process; Lead protocol development and writi

This position will work with the central scheduling manager with retrospective and active data entry to support Non clinical studies within an electronic database. Additionally, this position will support scheduling in vivo activities as needed to ensure a timely proposed schedule for non clinical study directors using project management software. The contract research ass

of Position Assist and support the Associate Director in managing Contract Development and Research Organizations (CDMO) in the areas of Clinical Supplies . Review master batch records (MBR), Master Packaging Work Orders (MPWO), and clinical related supplies related documents . Assist and support the review of packaging, labeling, storage, logistics, and distribution docum

Maintains the ordering and stocking of medications and supplies as needed in the clinic. Under supervision of appropriate licensed healthcare professional as defined by State regulations, prepares and mixes medications. Coordinates with drug sales representatives, and pharmaceutical companies to obtain samples, teaching aids, and compassionate drugs. Acts as liaison betwe