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Document Management Functions: Maintains the integrity of the Clinical Data Repository (CDR) with comprehensive Matter Expert knowledge of applications, workflow, and integration within Hyland OnBase, Solarity, and Maestro Care related to scanned document archival to troubleshoot user concerns.
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Review the New/Return patient form with the patient Complete global assessment for every return patient Complete a learning assessment for every patient on each encounter Assisting in tracking infection rates during suture removal Record vital signs, medication reconciliation and allergy identification.
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Design, oversee, and conduct classical and modern test theory analyses, interpretation of meaningful change, and post-hoc statistical analyses to support evaluations of clinical outcome assessments for regulatory review.
$100,000 - $165,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Calculates, measures, and documents appropriate values on the tests performed for review and interpretation by physicians. Communicates with physicians, managers, and co-workers as appropriate about changes in patients clinical conditions while undergoing echocardiogram.
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Serves as a member of the Development Team for Duke LifePoint Healthcare in the evaluation of potential hospitals including assisting in the development, and review of RFP responses, due diligence and go/no go recommendations.
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Qualifications: Educational, Certification & Licensure Requirements: - Certification through the American Board of Anesthesiology or specialty qualifications that are acceptable to the ACGME Review Committee - Academic credentials and experience to qualify for appointment at the rank of Associate Professor or Professor in the Duke University School of Medicine - Current and ongoing clinical activity in anesthesiology.
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Review and approve collateral material for the Clinical Affairs function. Support development and maintenance of systems (, electronic trial master file (eTMF), clinical trial management systems (CTMS), consultant management) to ensure effective management of clinical studies.
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Facilitating and coordinating communication with and among internal Duke business and legal stakeholders (, legal counsel, risk management, corporate compliance, administrators, business managers, program directors and clinical leaders) to ensure appropriate internal review and input for each contract.
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Provide assessment of batch acceptance and perform final batch disposition decision for clinical and commercial production batches. You will be responsible for the strategic and tactical oversight of batch documentation review, continual evaluation during batch production, as well as providing material acceptance decisions for production batches.
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Conduct regular contract review meetings with suppliers and key stakeholders to ensure performance meets expectations. As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas.
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Conduct batch record review for clinical and commercial product manufactured for Humacyte. Under limited direction and supervision, create, review, and revise standard operating procedures.
$80,000 - $81,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Strong clinical skills and proficiency in acute care management. Participate in quality improvement initiatives, peer review, and performance evaluation processes to monitor and enhance the quality and safety of patient care.
$260,000 a yearExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Under supervision, may perform TMF review and oversight at country and site level. Under supervision, may assist with clinical supplies (including medication) order, receipt, inventory storage, distribution, return/recall and reconciliation.
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Provide medical consultation and guidance to healthcare providers regarding complex patient cases, clinical protocols, and treatment options. Stay informed of industry trends, regulatory changes, and advancements in medical practice and technology, and incorporate best practices into clinical operations.
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Worked as the lead writer on >3 (Senior Medical Writer) or >5 (Principal Medical Writer) of at least 3 of the following: Clinical Study Protocols, Clinical Study Reports, Clinical Summaries in the CTD format, Investigator Brochures, IMPDs/INDs, scientific publications.
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review clinical jobs in Durham, NC
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