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The Research Nurse I will be responsible for rendering patient care services to patients on research protocols approved through the Northside Hospital IRB. Responsibilities involve patient registration, data collection, data submission, adverse event reporting, patient follow-up, records management, protocol regulatory management, quality assurance and other activities related to research.
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This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace.
$50,000 - $100,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Years’ experience: Minimum of two (2) years’ experience coordinating research protocols OR (2) years' experience in cancer research OR certification as a Certified Clinical Trial Investigator (CCTI), Certified Clinical Research Coordinator (CCRC), or Certified Clinical Research Professional (CCRP) from the Association of Clinical Research Professionals (ACRP) or the Society of Clinical Research Associates (SoCRA.
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Cancer Center in Northern, NJ area are seeking Oncology Clinical Research Nurses working with medical oncology, solid tumor patient population. Must have Oncology Clinical Research experience or someone who has a strong oncology nursing background and would be willing to be trained in clinical research.
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Bachelor’s degree and minimum of 2 years’ experience as a Clinical Research Coordinator/Clinical Research Associate OR. Associate’s degree and a minimum of 4 years’ experience as a Clinical Research Coordinator/Clinical Research Associate OR.
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Patient Experience Coordinator activities include greeting new admissions and ensuring all clinical and service-related needs are met by proactive rounding, anticipating, and identifying needs, soliciting input, and addressing any issues or concerns.
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This position is based in the Cancer Clinical Research Unit, with patient visits occurring in the downtown Seattle Virginia Mason outpatient oncology clinic. Minimum one year full-time related experience within clinical research.
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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 CRC B provides regulatory assistance to more junior clinical research coordinators, meets with external and internal study monitors as needed, participates in audit preparation, maintain records in audit ready condition, track patient visits and procedures for confirmation of proper billing process, documents research required training for staff and investigators (HIPAA, ICH/GCP as well as protocol specific training.
$43,919 - $66,183 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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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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3 years of experience in clinical research in a medical/behavioral setting with knowledge about the conduct of clinical trials, research principles, and methodologies/study design.
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Learn more about Clinical Research at MSK : Research is integral to our mission at MSK and clinical trials help us discover better forms of patient care and treatment.
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Qualifications KNOWLEDGE , SKILLS, AND ABILITIES REQUIRED:BA/BS preferred in public health or related field; Associates degree or equivalent work related experience required; Minimum of 2 years of experience in clinical or public health research.
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Under the general supervision of the Clinical Nutrition Manager (CNM)/Director of Nutritional Services. Performs and documents nutritional assessments according to the MNT protocol and Stormont Vail Health Standards of Care. Collaborates inter-professionally to plan and implement patient care.
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Minimum of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years related experience in the field of clinical research.
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clinical research patient experience jobs Title: research assistant Company: Care Access
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