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Licenses and Certifications Preferred: Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC.
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Moreover, the Estimating Coordinator is the forward face of Adams Group and are responsible for establishing a professional work environment that includes, fostering a positive atmosphere, promoting proactive and effective communication, facilitating problem solving and for minimizing and resolving conflicts.
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It has direct responsibility for implementing a diverse portfolio of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or programmatic clinical research activities, such as a clinical database and biorepository.
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Preferred: Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) is preferred. Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) certification, along with a minimum of two years additional professional experience, will be considered in place of degree.
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The primary responsibility of the Clinical Research Coordinator I is to assist in managing all aspects of conducting clinical trials. As one of the primary resources for the protocol, the Clinical Research Coordinator I acts as a liaison between the patient, investigator, Institutional Review Board and sponsor.
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Clinical Research Coordinator for Large Neuroimaging Study of Aging and Alzheimer’s disease. The Mormino Lab within the Department of Neurology and Neurological Sciences is seeking a Clinical Research Coordinator Associate (CRCA) to work on new projects involving high-frequency data collection in older adults.
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Keywords: #indeed, Monster, Talroo-allied health, epidemiology, clinical research specialist, clinical research coordinator, public health, research project lead. Sentara Health sClinical Trials Office located at Sentara Norfolk General Hospital is hiring a Research Outcomes Data Coordinator.
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Qualifications Supervisory Skills and Communication Experience operating heavy equipment 5 years experience in site work , underground utilities or concrete work Ability to read blueprints and understand job specifications Strong organizational and problem solving skills Ability to work independently as well as with a team Valid drivers license Understand production goals and how to meet them Understand Project schedules Powered by JazzHR.
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Job Description Grow your career at Cedars-Sinai Join our team and use your skills with an organization known nationally for excellence in research This position functions as a Clinical Research Finance Coordinator (CRFC) responsible for coordinating and executing the financial billing of clinical trials.
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The University of Pennsylvania's Center for Weight and Eating Disorders seeks a part-time Clinical Research Coordinator to participate on studies of the treatment of obesity, under the direction of Tom Wadden, PhD, Ariana Chao, PhD, CRNP, and Sharon Leonard, RD. The Coordinator will work on two or more industry-sponsored trials that are assessing behavioral and pharmacological interventions for obesity.
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Provide in-person assessment, triage, crisis intervention and problem-solving services for LEAD participants experiencing complex health, mental health and/or substance use challenges. Active/Valid BBS license as a Licensed Clinical Social Worker (LCSW) or Licensed Marriage and Family Therapist (LMFT.
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The primary responsibility of the Clinical Research Coordinator is to manage all aspects of conducting clinical trials. As the primary resource for the protocols, the Clinical Research Coordinator will act as liaison between the investigators, primary care providers, the institutional review board (IRB), and the sponsor.
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Healthy Brain Clinic, a research site specializing in clinical trials of Alzheimer's Disease, is seeking applicants for a Clinical Scientist (Psychological Rater). Higher salary is negotiable with candidates who have experience with Psychometrician / Psychological Rater experience in pharmaceutical clinical trials.
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The EHS Coordinator must be able to align the site s EHS activities with Valmont s overall environmental, health and safety strategies. The EHS Coordinator will interact with site production employees to identify and control hazards that can result in harm.
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The Residency Program Coordinator must demonstrate initiative, resourcefulness and problem solving skills by applying a detailed knowledge of the ACGME Resident Review Committee (RRC) program requirements (PR) and Common Program requirements (CPR.
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