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Responsibilities: Conducting all trial visits Completing all study-specific assessments (e.g. vital signs, EKG, blood collection) Processing all samples and shipping to Central Lab Maintaining study source Entering data into sponsor EDC and query resolution as the sole Senior Clinical Research Coordinator (SCRC) on-site, the chosen candidate must be adept at protocol comprehension and be capable of working autonomously.
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Our core practice areas include vaccine research, development, and production; microbiology and infectious disease research; biodefense; clinical research; global health security; and HIV/AIDS programs.
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Job Description: The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as documenting and reporting on the daily operations of assigned trials.
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Licensed Mental Health Professional (CA Department of Health Care Services): Licensed Clinical Social Worker (LCSW), or; Licensed Professional Clinical Counselor (LPCC) recognized by the Department of Health Care Services (DHCS); or Certified as an Alcohol and Drug (AOD) counselor at the CADC II level with a certification recognized by the Department of Health Care Services (DHCS.
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The clinical role of this position at LAC+USC Medical Center will consist of cancer genetic counseling services in a busy academic clinical medical oncology setting. The genetic counseling position is comprised of both research and clinical roles.
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Job Summary The Clinical Research Coordinator will support the research programs of Dr. Garber, including multi-site, NIH-funded studies of refeeding in body composition in anorexia nervosa, and a new pilot study on microbiome recovery in malnutrition.
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Rush University Medical Center , a nationally recognized clinical and academic institution and the teaching hospital for Rush Medical and Nursing Colleges, located in downtown Chicago, invites applications for the position of Instructor, Gender Affirmation Surgery in the Division of Plastic and Reconstructive Surgery, with a start date of July 1, 2025.
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MINIMUM QUALIFICATIONS Valid California Clinical Laboratory Scientist (CLS) license or limited CLS license in Histocompatibility. Certification by the American College of Histocompatibility and Immunogenetics (ACHI) as a Certified Histocompatibility Technologist (CHT) or ACHI Certified Histocompatibility Specialist (CHS) or certification as a Medical Technologist by the American Society of Clinical Pathologists, MT(ASCP.
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Frye Regional Medical Center employs more than 1500 professional and clinical staff. Responsibilities include: establishing and maintaining accurate and compliant policies, procedures and protocols related to sample collection and phlebotomy practices; supervision (clinical) of the phlebotomy team; timely review of periodic reports/temp logs and other data related to phlebotomy, and performs tasks in a safe manner and in accordance with all safety and health programs.
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Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Histotechnology, Medical Technology or meet local regulatory (CLIA & State) requirements. Provide leadership and direction to cytology, histology, IHC, and transcription departments across multiple sites, ensuring consistent, high-quality service delivery.
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The Sr Clinical Trial Manager is accountable for delivery of selected and/or regional activities within a trial (e.g., manage and oversee vendor deliverables, collaborate with functions to set up activities [e.g. DM, IRT, eRT], support site activation and recruitment, support data review/cleaning activities, support PI/ICF development.
$190,625 a yearFull-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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The department of Computational Biology is seeking an experienced lead or principal-level bioinformatics research scientist to provide direction and lead the development of pipelines for use in our clinical genomics program.
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Strong knowledge with CDISC (CDASH/SDTM), medical dictionary coding standards, FDA and ICH guidelines, GCP, 21 CFR Part 11, Clinical Data Management best practices. Liaise directly with internal customers (Biometrics, Clinical Operations, Safety/Pharmacovigilance, Regulatory Affairs, etc.
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Basic Qualifications: Experience Minimum two (2) years post masters practice experience as a Licensed Clinical Social Worker OR Licensed Professional Counselor OR Licensed Marriage and Family Therapist.
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One year of approved clinical laboratory experience, which must include a clinical rotation through the following sections of the laboratory: Blood Banking, Microbiology, Chemistry, and Hematology, Immunology, and Urinalysis/Body Fluids in the U. S. or with an accredited laboratory within the last 5 years.
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Title: clinical Company: Wellness Healthcare Solutions
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