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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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Date Posted Friday, January 12, 2024 Position is with Lab/Branch/Program Name of Hiring Official/Investigator Job Description A postdoctoral position is available in the lab of Dr. Stavroula Mili in the Laboratory of Cellular and Molecular Biology, National Cancer Institute, NIH, Bethesda, MD.Dr. Mili's research program focuses on the roles of localized mRNAs in mammalian physiology and tumor progression.
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Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues.
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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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Description The Clinical Research Nurse Program Manager (CRNPM) is responsible for the management and overall direction of large and complex research projects, in close collaboration with the clinical investigator, including the day-to-day operations of large research programs following Good Clinical Practice (GCP) guidelines.
$150Full-timeExpandUpdated 1 month ago - UpvoteDownvoteShare Job
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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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Management of Clinical Trial PatientsCollaborates with the investigator to ascertain study patient eligibility for a clinical trial, including documentation of criteria specified in the protocol.
$70,000 - $90,000 a yearExpandUpdated 1 month ago - UpvoteDownvoteShare Job
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Gather and analyze data resulting from the collaborative research to be used for identifying disease protein profiles and biochemical and metabolic changes to complete the clinical characterization, as well as metagenomics/ microbiome sequencing.
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The Research Assistant will develop a progressive functional knowledge of Good Clinical Practices (GCP), Office of Human Research Protections (OHRP) regulations and Food and Drug Administration (FDA) regulations.
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Therefore, the section chief will be responsible for tool development that highlights, flags or streamlines safety issues and will lead clinical safety protocol activities within DCI. The position will be within the Clinical Affairs Branch of DCI, which supports the NCATS Trial Innovation Network andThe Helping to End Addiction Long-term Initiative, or NIH HEAL Initiative.
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The section chief will serve as a senior leader, representing DCI and NCATS in clinical, research and clinical trial training/career development programs across NIH, other government agencies, industry, academia and patient-support organizations.
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Provide general insight into GSK research interests and field inquiries regarding investigator sponsored scientific or clinical research projects. Attend and contribute (if required) to medical portion of regional account planning/training sessions Attend both national and regional scientific/medical meetings to gain medical voice of the customer on recent data being presented on products and disease states of interest to GSK Support clinical development activities and programs including GSK and Investigator sponsored studies as well as collaborating with R&D staff to improve site performance.
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The Clinical Research Coordinator participates in or leads day-to-day operations of clinical research studies conducted by a principal investigator. The Research Coordinator will develop a progressive functional knowledge of Good Clinical Practices (GCP), Office of Human Research Protections (OHRP) regulations and Food and Drug Administration (FDA) regulations.
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Job responsibilities are similar to the following positions: Research Scientist, Principal Investigator, Associate Professor, Clinical Researcher. Doctoral degree and 7+ years of experience in a research discipline relevant to patient-centered outcomes research (e.g., clinical epidemiology, health services research, sociology, psychology, health policy, biostatistics, economics, bioinformatics, data science, education, or health education.
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The Research Associate Scientist will perform experiments using animal models and clinical tissues obtained from clinical trials to uncover how tumor-fighting immune cells arrive at and function within tumors.
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clinical investigator jobs in Mclean, VA
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