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Informs Investigator Initiated Study (IIS) strategy and can act as Docent for IISs. The Associate Scientific Director provides medical and scientific strategic and operational input into core medical affairs activities such as: health-care professional and provider interactions (HCPs, Patients and Payers); generation of clinical and scientific data (enhancing therapeutic benefit and value); educational initiatives (medical education, data, guidelines, and value proposition); safeguarding patient safety (risk minimization activities and safety surveillance activities.
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As lead of the Study Core Team the CS will lead via a matrix organization Epidemiology, Biostats, Clinical Operations, Medical/Scientific Affairs, Regional, Pfizer laboratory assay group, and external team members.
$145,400 - $269,400 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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This clinical research coordinator (CRC) position may provide study coordination for multiple clinical research studies depending on complexity that range from moderate to complex.
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Proven proficiency in survey research methodology/research study design, hypothesis testing and qualitative data interpretation and application. Provides input towards study design, develops analysis plans and interpretation of study results for review of Senior Scientist; may include presentation to TPMG, KFH/P managers and committees.
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These activities may occur at various stages of the clinical trials, including study start-up, maintenance, close-out, and/or archival. High school diploma/GED and at least 2 years of relevant experience in clinical trials research.
$29 - $34 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Requires basic knowledge and techniques to conduct various experiments in molecular biology and protein chemistry and the ability to adapt to new technologies related to the research projects. Experience Required: Five years of experience in scientific or experimental research work.
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May collaborate with study investigators, nurses, study coordinators, and study sponsors to coordinate study start-up activities, which include collection and distribution of regulatory, budget, contract, and coverage analysis documents.
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Here, you can apply your scientific curiosity in Biology, Animal Science, Zoology, Animal Behavior, Veterinary Technology, Dairy Science, Equine Science or similar majors to pursue advances in animal welfare and research the effectiveness, safety and toxicity of drugs in early development animal research studies.
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Works directly with investigators and study team members on the development and revision of clinical research protocols and Informed Consent Forms (ICFs), and facilitates the activities of writing and regulatory review with bi-directional dialogue and feedback.
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Ability to work in a clinical research setting with multiple teams independently and within a team to facilitate efficient completion of study tasks. The Frederick National Laboratory is a Federally Funded Research and Development Center (FFRDC) sponsored by the National Cancer Institute (NCI) and operated by Leidos Biomedical Research, Inc. The lab addresses some of the most urgent and intractable problems in the biomedical sciences in cancer and AIDS, drug development and first-in-human clinical trials, applications of nanotechnology in medicine, and rapid response to emerging threats of infectious diseases.
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Provide training on the Diplomatic Security Identity Assurance System (DSIAS) to students attending the Basic RSO, RSO In Service, Assistant Regional Security Officer-Investigations, Foreign Service National Investigator, and Foreign Service National Investigator In Service training classes at the Diplomatic Security Training Center.
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Under the general supervision of the investigator, performs complex laboratory experiments in the field of cell biology including: cell culture, ELISA, DNA/RNA isolation, PCR, general biochemistry, immunohistochemistry, flow cytometry, and microscopy.
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Research Engineer serves as principal investigator for multiple research projects investigating electronic assembly processes, assembly materials, interconnect reliability or novel assembly manufacturing equipment as they relate to existing or developmental electronic packaging technologies.
$92,000 - $107,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Clinical Trial Manager, Site Start-up will lead internal process improvements related to study start up activities to ensure clinical trials are executed with high quality standards in compliance with regulatory requirements, GCP, and company SOPs.
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The scope of responsibility for a Research Interventionist is greater than that for a Clinical Research Specialist due to any combination of the following: greater level of independent safety or clinical decision making required; greater level of specialized clinical knowledge required; substantial contribution to areas such as project intervention materials, plans, study design and research papers; and comprehensive consultation role on policies and methodology.
$54,000 a yearFull-timeExpandUpdated Today
clinical research investigator study start up jobs Company: Cedars Sinai
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