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The Staff Scientist I is a junior career research position that reports to the principal investigator. Conducts research and development of new next generation sequencing clinical assays.
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Uses accepted methods and techniques, solves well-defined problems and performs specific and limited portions of broader projects under the technical guidance of the principal investigator and the senior staff scientist.
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Accredited Healthcare Fraud Investigator (AHFI), Health Care Anti-Fraud Associate (HCAFA), Certified Insurance Fraud Investigator (CIFI), Certified Financial Crimes Investigator (CFCI), Certified Fraud Examiner (CFE), and Certified in Healthcare Compliance (CHC) Certifications.
$75,600 - $172,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Maintain communication with the principal investigator and clinical research coordinator regarding study and enrollment. Assist the principal investigator and clinical research coordinator with management of day-to-day operations related to clinical research projects in the ED.
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We are examining therapeutic targets for traumatic brain injury (TBI) and evaluating candidate therapeutics for repurposing to TBI as a new clinical indication. The person selected for this position will conduct research in experimental models to screen therapies to promote regeneration and plasticity to protect against neurodegeneration and chronic symptoms associated with traumatic brain injury (TBI) and related clinical conditions.
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Assists in the preparation of new drug application safety updates, investigational new drug safety reports, investigator communication, product labeling/package inserts, and other reports as necessary.
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Proven experience in hematology/oncology drug development, designing and managing clinical trials (Ph 1b/II and Ph III) through investigator and regulatory interactions; experience with early-clinical development, including FIH and IND, is a plus.
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General Summary of Position Under the direction of the Principal Investigator (PI) and within the scope of nursing practice, the competent Clinical Research Nurse Coordinator I (CRNC I) with moderate supervision, assesses, plans and implements and evaluates the nursing care of potential research participants from pre-screening through study exit.
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Clinical Research Nurse, Clinical Research Unit - Georgetown University Medical Center. The CRN operates as part of a team of both nursing staff and research assistants who assist the study coordinator and Investigator in protocol implementation.
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The successful candidate will work under the direction of the Principal Investigator of the Laboratory of Vascular Thrombosis and Inflammation. The faculty in the NHLBI DIR is an outstanding group of internationally recognized biomedical researchers covering a wide range of basic and clinical research topics (please see ) complemented by the other research institutes within the DIR (please see.
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Tracks site budget and investigator grant estimates when needed via Medidata Grants Manager. Emmes requires all US based Clinical Research Associate new hires to be fully vaccinated before their first day of employment.
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With over 40 research groups conducting basic neuroscience research and clinical investigations of mental illnesses, brain function, and behavior. May serve as an associate or principal investigator for specific protocols, or assist with IRB and regulatory documentation for protocols the service is involved in.
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Write or lead all aspects of the writing of clinical study reports and Investigator Brochures for products in all phases of clinical development (phases 1-4) + Write CTD sections including the Summary of Clinical Efficacy, Summary of Clinical Safety, Summary of Clinical Pharmacology, Summary of Biopharmaceutics, Clinical Overview, Table of All Studies, briefing documents, and safety narratives.
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The MEL conducts critical activities that support advancing science, educating on evolving clinical practices, transforming science into patient care, and facilitating the development of new research collaborations (including Investigator Initiated Trials and Real-World Evidence.
$270,000 - $305,000 a yearPart-timeRemoteExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Clinical Research Coordinator I will perform delegated duties such as protocol required visit procedures, administering questionnaires and subject material, administering, and dispensing medication, adhering to regulatory guidelines, and participating in subject recruitment efforts, under the oversight of the study Principal Investigator.
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clinical investigator jobs in Silver Spring, MD
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