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The Senior Principal Scientist at Amgen is responsible for clinical pharmacology components of multiple clinical programs, including study design, protocol preparation and reporting. Plans timing for, designs, leads, and may act as clinician for healthy volunteer phase I and dedicated Clinical Pharmacology studies including (but not limited to) SAD/MAD, DDI, Food-Effect, ADME, Hepatic/Renal Impairment, BA/BE, and PK bridging.
$162,147 - $189,560 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Responsible for assisting the Study Director in the reporting of protocol/ SOP deviations and responding to Study Audits and findings. Compile all report comments and assure they are conveyed to the Study Director at the CRO Responsible for assisting in the management of all aspects of the studies, including data quality and integrity, efficiency, and regulatory compliance in the execution of study protocols.
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In Vivo Study Monitor Kelly® Science & Clinical is seeking In Vivo Study Monitor for a position at a Biotech company in Thousand Oaks, CA. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.
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Collaborate with cross-functional teams on protocol review, testing preparation, change control process, and deviation & CAPA. Collaborate with cross-functional teams on protocol review, testing preparation, change control process, and deviation & CAPA.
$35.98 an hourExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Collect, process and ship specimens as directed by protocol, under the direction of the CRC. Complete visit procedures as required by protocol, under the direction of the CRC. The Clinical Research Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while learning the skills necessary to be a Clinical Research Coordinator.
Full-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Author and revise controlled documents (SOPs, PCSs, RPTs, APPXs) in CDOCS and PLM system. Author and revise controlled documents in document management system. Under supervision by senior personnel, the individual will apply engineering principles and follow current SOPs to help execute the design, qualification and implementation of thermal packaging systems.
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Experience in animal husbandry/in-vivo study conduct within Toxicology strongly preferred. Kelly® Science & Clinical is seeking In Vivo Study Monitor for aposition at a Biotech company in Thousand Oaks, CA. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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With minimal supervision, plans, conducts or monitors experiments, records and organizes data, analyses results, generates robust and reliable data and/or Ensures that contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations.
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As a travel physical therapist with Nomad, youre expected to communicate and document all required details as per facility charting protocol, monitor patients condition and assess needs to provide the best possible quality of care, and deliver age-specific direct patient care according to unit scope of service.
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Skills: ; degree in Biology, Biochemistry or Analytical Chemistry ; experience in a Biopharmaceutical working environment. Supporting a protein microarray screening platform to Client Client molecular glues as a new therapeutic modality based on targeted protein degradation.
ExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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You will be responsible for planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP.
$32.65 - $52.53 an hourExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Answers, screens, and forwards incoming phone calls in accordance with National Vision protocol. Experience as a Receptionist, Front Office Representative or similar role preferred but not required.
Part-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Clinical Pharmacology, Modeling & Simulation- Senior Principal Scientist page is loaded. Clinical Pharmacology, Modeling & Simulation- Senior Principal Scientist. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.
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Follows the clinical standards of care for the center, including, but not limited to operating practices and procedure, incident tracking/reporting, quality maintenance, surgical protocol, updating medication protocol, patient, and occupational health and safety.
$125,000 - $135,000 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Experience with NASA World Wind Java, ATAK, Cesium, Protocol Buffers, Avro, OpenGL/OpenCL, and/or CUDA. Experience with NASA World Wind Java, ATAK, Cesium, Protocol Buffers, Avro, OpenGL/OpenCL, and/or CUDA.
$150,000 - $200,000 a yearFull-timeExpandApply NowActive JobUpdated 9 days ago
protocol job in Newbury Park, CA
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