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Under the guidance of the CRD he/she collaborates with the Coding specialist, Biostatisticians, Data Managers, Global and Regional Study Managers, Feasibility Managers, Pharmacovigilance representative, Medical Writer (e.g. planning and review of narratives) on high quality medical review, as needed.
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He/she supports the CRD to ensure appropriate documentation and consistency of the data and investigations of safety cases with the Clinical Trial Team (Monitoring Teams) or Pharmacovigilance. He/she supports the CRD to ensure appropriate documentation and consistency of the data and investigations of safety cases with the Clinical Trial Team (Monitoring Teams) or Pharmacovigilance.
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This role is key to help the medical supervision of clinical studies by Clinical Research Directors (CRD) and to ensure scientific management of clinical studies to be performed by the Clinical & Sciences Operations Platform (CSO) and Development Units in.
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Lead implementation and delivery ensuring coding, unit testing, system integration, defect resolution, and technical documentation adheres to our standards. Promote shared ownership of code though code reviews, standards, and documentation.
Full-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Contribute to definition of the centralized monitoring strategy in consistency with the planned statistical analysis and is involved some of the study data validation and review processes, support the CRD for the Clinical Case review (safety events reported to Pharmacovigilance or safety events of special interest.
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This role is key to help the medical supervision of clinical studies by Clinical Research Directors (CRD) and to ensure scientific management of clinical studies to be performed by the Clinical & Sciences Operations Platform (CSO) and Development Units in Client R&D.
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This role is key to help the medical supervision of clinical studies by Clinical Research Directors (CRD) and to ensure scientific management of clinical studies to be performed by the Clinical & Sciences Operations Platform (CSO) and Development Units in company's R&D.
$55 - $82 an hourExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Previous experience in Clinical Research and/or Drug Development (e.g., at least 5-10 years within pharma industry or CRO or other clinical trial sites). The applicant must be familiar with all medical and operational aspects related to the conduct of late-stage clinical trials.
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This role is key to help the medical supervision of clinical studies by Clinical Research Directors (CRD) and to ensure scientific management of clinical studies to be performed by the Clinical & Sciences Operations Platform (CSO) and Development Units in R&D.
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Open to candidates willing to relocate at their own expense Must be able to start ASAP Paid parking is required on-site Hybrid, a minimum of 2 days onsite (with flexibility to adjust due to business needs, required meetings etc.
$70 - $80 an hourExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Finance team is looking for an Accounts Payable Specialist who will be responsible for general ledger coding of invoices, inputting invoices for payment, and preparing documentation for payment of invoices.
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Under the guidance of the CRD candidate collaborates with the Coding specialist, Biostatisticians, Data Managers, Global and Regional Study Managers, Feasibility Managers, Pharmacovigilance representative, Medical Writer (e.g. planning and review of narratives) on high quality medical review, as needed.
$85.52 - $89.52 an hourExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Identifies when documentation relevant to coding the procedure is missing, lacks specificity, or is inconsistent and communicates with physicians via EPIC in basket messaging to obtain the missing information.
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Oversee, develop and maintain study-specific documentation, including Data Management Plans, eCRF specifications, CRF Completion Guidelines, Data Validation Guidelines, Data Transfer Specifications, Coding Guidelines, Post Production Database Change Control Documentation, Database Audit and Lock Procedures.
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You will be involved in all stages of the development and execution of studies such as conducting literature reviews, developing study protocols (qualitative and quantitative), developing statistical analysis plans, preparing study documentation for ethical review, interviewing clinical experts and patients, qualitative coding and analysis, reporting results, and writing presentations, conference abstracts/posters, and journal manuscripts.
$29ExpandApply NowActive JobUpdated Yesterday
documentation coding jobs in Boston, MA
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