- Daiichi Sankyo, Inc. (Bernards, NJ)
- …document. Collaborates as team member with AROs/CROs. Drafts development plans, protocol profiles, and sections of submission documents under guidance of higher ... data quality listings, SAP, Data Mgmt plan; Reviews patient population and protocol compliance for consistency with study strategy; Develops biomarker strategy in… more
- Merck & Co. (Rahway, NJ)
- …activities.Job ResponsibilitiesResponsible for the clinical/scientific execution of clinical protocol (s).Serves as the lead clinical scientist on the clinical ... medical monitoring team in review and interpretation of clinical data/medical protocol deviations in collaboration with the Clinical Director.Builds talent and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …works under some supervision to solve complex study problems. Responsibilities Protocol Development, Case Report Form (CRF; review), Statistical Analysis Plan (SAP), ... Leads statistical activities for complex studies including study design, protocol development, CRF review, SAP development, analysis files development, statistical… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …tasks- Backfill leader of Facilities Services on projects as needed- Security, Protocol and Reception- Partner with Security to support coverage for Reception at ... the front desk, including the greeting of visitors and employees, management of deliveries, and answering phones when needed- Partner with Security to facilitate and execute emergency management and safety procedures- Support Security manager with security… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …statistical activities for medium complexity studies including study design, protocol development, CRF review, SAP development, analysis files development, ... statistical analysis accuracy validation, results interpretation and CSR input and review. Acts as main statistical contact for the assigned studies and projects. Provides guidance to study team on all aspects of statistical activities; collaborates closely… more
- Novo Nordisk Inc. (WA)
- …of data collected at clinical trial sites in accordance with the protocol , Monitoring Plan and other associated trial documents Complies with relevant training ... of medical and scientific concepts in order to effectively interpret protocol requirements, support sites and effectively conduct monitoring activities. The CRA… more
- Aequor (South San Francisco, CA)
- …that contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations. Responsibilities include: ? Monitors or ... follows established experimental design and protocols and performs routine tasks and studies to obtain reproducible and reliable results with limited supervision ? Plans, monitors or conducts, analyzes and records experiments, and provides interpretation of… more
- Merck & Co. (North Wales, PA)
- …interprets results from clinical trials to meet objectives of the study protocol .- Independently applies and implements basic and complex statistical techniques to ... these analyses.Prepares oral and written reports to effectively communicate results of clinical trials to the project team, company Management, regulatory agencies, or individual investigators.Provides responses to queries relating to study design, analysis,… more
- Aequor (Thousand Oaks, CA)
- …that contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations. Responsibilities include: ? Monitors or ... follows established experimental design and protocols and performs routine tasks and studies to obtain reproducible and reliable results with limited supervision ? Plans, monitors or conducts, analyzes and records experiments, and provides interpretation of… more
- Novo Nordisk Inc. (Irvine, CA)
- …of data collected at clinical trial sites in accordance with the protocol , Monitoring Plan and other associated trial documents Complies with relevant training ... of medical and scientific concepts in order to effectively interpret protocol requirements, support sites and effectively conduct monitoring activities. The CRA… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …role is primarily a tactical study delivery role, reporting into an Associate Director (or above) responsible for Operational Study Strategy. This position may ... activities conducted by CROs and vendors.Provide operational input into study protocol profiles, final protocols and amendmentsLead document review & coordination… more
- Shimadzu Scientific Instruments (Tampa, FL)
- …training. EDUCATION AND/OR EXPERIENCE REQUIREMENTS: Incumbent should have at least Associate degree in Electrical Engineering or Technology; while a bachelor's ... to maintain proper housekeeping and safety standards in particular to lab safety protocol . Proper use of personal protective equipment and safety devices as required… more
- Shimadzu Scientific Instruments (Long Island City, NY)
- …necessary, customer and staff training. EDUCATION AND/OR EXPERIENCE REQUIREMENTS: An associate 's degree in Electrical Engineering or Technology with preferably at ... to maintain proper housekeeping and safety standards in particular to lab safety protocol . Proper use of personal protective equipment and safety devices as required… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Global Safety Lead(s), Global Safety Lead(s) and Global Safety Scientist(s)/ Associate within Safety Surveillance. Essential Functions Innovation and change ... Provide safety input to Product Development Plan (PDP), Trial Outline, Protocol , Clinical Trial Report, Investigator's Brochure (IB), integrated safety summaries,… more
- TalentBurst, Inc. (Newark, CA)
- Title: Research Associate ILocation: Newark, CA 94560Duration: 6 Months+Job SummaryUnder the direction of the Associate Director of QC Bioassays or department ... research and experiments following established protocols and SOPsThe Research Associate I will perform routine laboratory and equipment maintenance, assist… more
- Careers Integrated Resources Inc (Newark, CA)
- Job Title: Research Associate I (QC Bioassays) Job Location: Newark, CA, 94560 Job Duration: 06 months (possible extension) Payrate- 30-34/hr on w2 Job Summary Under ... the direction of the Associate Director of QC Bioassays or department manager, perform...Understand and follow relevant Standard Operating Procedures (SOPs) and Protocol requirements regarding all laboratory activities assigned or engaged… more
- University of Maryland Medical System (Baltimore, MD)
- …Schwartz Division of Transplantation, home to Maryland's first steroid-free protocol and pancreas/kidney transplant. From our National Cancer Institute-designated UM ... 3. Unit Management A. Notifies Chief Tech/Team Leader of requests for protocol changes. B. Communicates with clinicians regarding patient preparation for procedures.… more
- Blanchard Valley Hospital (Findlay, OH)
- …JOB DUTIES/RESPONSIBILITIES Duty 1: Organizes department. Develops orientation protocol . Orients and teaches students as necessary. Regularly demonstrates ... data. JOB DUTIES/RESPONSIBILITIES Duty 1: Organizes department. Develops orientation protocol . Orients and teaches students as necessary. Regularly demonstrates a… more
- Blanchard Valley Hospital (Findlay, OH)
- …daily oversite of clinical laboratory section and associates. Develops orientation protocol . Orients and teaches students and new associates as necessary. Regularly ... responsibilities to promote smooth operation of the department and growth of associate 's work experience. Provides immediate direction to duty assignments of all… more
- University of Maryland Medical System (Baltimore, MD)
- …Schwartz Division of Transplantation, home to Maryland's first steroid-free protocol and pancreas/kidney transplant. Our National Cancer Institute-designated UM ... to interns and students. Qualifications Education and Experience Education: Associate degree (required) Bachelor's Degree in Respiratory Therapy (preferred)… more
