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CommunicationIndependently/collaboratively performs responsibilities of Level I.Collaborate closely with study coordinator on patient updates and clinical issues to ensure prompt, accurate reporting to sponsor or other entities is handled within protocol/ regulatory guidelines.
$72,940 - $100,380Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Senior Research Coordinator will ensure precise implementation of and adherence to study protocol, create all study documentation, oversee operating procedures, timelines, IRB applications, data preparation, and other research-related activities.
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Enter study participants in the study participant tracking system, and study logs, maintain appointment calendarsConduct screening visits and study protocol specific study participant visits, assist staff physicians in assessment of concomitant medications, adverse events, lab results, and other test results.
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Be compliant with infection control procedures and environmental safety protocol within a facility. Build a strong physical therapy program Enhance clinical expertise, professional and management skills through interaction with managers, therapists and other professional staff, self-study, and other continuing education activities.
$33 - $49 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Conduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, inspection of study files, and related monitoring functions.
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Substantial clinical study protocol experience, as lead author, required. Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias.
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Review study protocol for feasibility of conducting study at Axon Clinical Research. Oversee and/or Conduct outpatient study procedures, as required by specific research project/protocol.
Part-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Prepares for upcoming study visits: research bio-specimen collection order preparation/placement, laboratory and EKG order placement, scheduling of biopsies and scans, interpreter requests, facilitating tumor assessment form completion from the investigator, QOL, AE and ConMed form completion in conjunction with a licensed professional (CRN/APP/MD) and other tasks as needed to support seamless, safe, and compliant clinical research conduct per protocol.
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Assists in the implementation and operation of all aspects of the OPTIONS study; operationalizes protocol based on study objectives, sound research principles and regulatory requirements under the direction of the Principal Investigator.
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Provides assessments and ensure protocol compliance while participants are in a study. May also assist with providing assessments and ensuring protocol compliance while participants are in a study.
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Collaborate closely with study coordinator on patient updates and clinical issues to ensure prompt, accurate reporting to sponsor or other entities is handled within protocol/ regulatory guidelines.
$72,940 - $100,380 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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The Feasibility Strategic Analytics Lead (FSAL) (Sr. Manager) will be responsible for partnering with Clinical Study Team Lead (CSTL), Participant Recruitment (PR), GSSO roles, and Clinical Leads to enable the predictable delivery of Pfizer’s portfolio by providing rapid, accurate and robust assessments of program and protocol feasibility, recruitment enrollment assumptions, and site strategy plans.
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Demonstrated understanding of the overall drug development process with clinical trial design, study implementation, sponsor/site interactions, scientific and clinical methodology, protocol design, project management and regulatory requirements for clinical studies to be reviewed by health authorities.
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Develops and prepares study or research related documentation such as protocol worksheets, procedural manuals, adverse event reports, case report forms, and institutional review board documents.
$56,000 - $62,000 a yearFull-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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The CRC follows protocol, institutional and regulatory requirements to assure accuracy of the study procedures being conducted. CRC conducts day-to day activities of multiple studies with respect to compliance, regulatory, recruitment, study site initiation, monitoring and close out throughout the course of the research trials.
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protocol study jobs in Baltimore, MD
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