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Assist Clinical Scientist, Study Responsible Scientist (SRS), &/or Study Responsible Physician (SRP) in various clinical research assigned Immunology Development clinical trials. Assist with clinical study activities such as study start up, investigator meetings, data review, etc.
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The Clinical Research Coordinator II conducts and manages multiple clinical trials from start up through study close out in accordance with the study protocol, GCP, and Velocitys SOPs. Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelinesand Velocitys SOPs.
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Provides diagnostic information by exposing and developing radiographic studies, pouring, trimming, and polishing study casts. Greater Maryland Oral Surgery and Dental Implants is looking for a Full-time Surgical Dental Assistant to support our office located in Gaithersburg 20879, Maryland.
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May study and test for additional licenses (Series 7 and Series 66) once the minimum licensing requirements are met. Current registration for FINRA Series 6 and Series 63 (or FINRA recognized equivalents) is required for this role or must be completed within a specified period.
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May perform study director/PI activities such as:Controls appropriate bioanalytical portion of studies by designing the experimental approach, overseeing the experimental execution, collating and interpreting scientific data and generating study reports, working in close co-operation with study Sponsors at all stages.
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Conduct analysis of cyber threats and IT vulnerabilities on government systems; develop, monitor, detect, report and investigate security breaches; in-depth study and investigation of Governance Risk and Compliance; evaluate and recommend new and emerging security products to design and build secure systems.
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OR You may substitute education for specialized experience as follows: A master's or equivalent graduate degree in a field of study that demonstrates the knowledge, skills, and abilities necessary to do the work of this position such as: human resources, public administration, organizational psychology, or other administrative and management fields.
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Deep chemistry and pharmacology knowledge and experience, including dose calculations and study conduct. Preparation/disposal of test materials/vehicles/reagents according to study protocols/SOPs.
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Director, Clinical Outcome Assessments (COA) And Value & Real World Evidence (VRWE) Study Management
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Knowledge of HEOR study design and conduct using real world data to generate evidence. Excellent knowledge of clinical development and research study designs and interpretation. The Director, COAs & Global Study Management will contribute to relevant components of Clinical Development trials that address GVRWE considerations.
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Experience with engineering calculations such as: load flow, short circuit and reactive capability analysis (ETAP or SKM), Arc flash analysis (ETAP or SKM), Cable ampacity study (CYMCAP or equivalent), grounding analysis, AC-DC voltage drop calculations, VOC/ISC calcs, AC/DC Cable sizing.
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Assist with the collection of study data as required by the study protocol, specifically the CBH screening form, admission forms and release of information. Complete other study procedures such as weight/height, waist/hip circumference as specified on the appropriate flow sheets.
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A Juris Doctorate (JD), Master of Laws (LLM), or Master's degree in Accounting or Taxation field of study will be considered in lieu of a Bachelor Degree in Accounting. A Juris Doctorate (JD), Master of Laws (LLM), or Master's degree in Accounting or Taxation field of study will be considered in lieu of a Bachelor Degree in Accounting.
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Maintain a vital and growing personal walk with the Lord through committed personal Bible study, prayer, and meditation. Maintain a vital and growing personal walk with the Lord through committed personal Bible study, prayer, and meditation.
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You will study part-time towards an Associate’s degree (AAS) in Biotechnology or Engineering Technology at one of GSK’s partnering community colleges fully funded by GSK- NO COLLEGE DEBT. Upon completion of the program, you will also receive a Certificate of Apprenticeship Completion from the US Department of Labor, an industry-issued, portable nationally recognized credential that certifies occupational proficiency.
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Support in vivo oncology research studies in mice as a member of the Study Services Team. Perform general study preparation and organizational activities, including sample tube labeling, supply organization and stocking, and laboratory organization.
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study job Company: National Gallery Of Art in Gaithersburg, MD
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