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You are a RN or Certified Nurse Midwife (CNM) with 3+ years of obstetrics or maternal fetal clinical experience. This includes designing the overall strategy for participant and clinician engagement, and defining the clinical components and structure for our maternal health programs.
$109,000 - $187,000 a yearFull-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Accountable in partnership with the Clinical Scientist and Statistician for the design, execution, and analyses of each study led by the CTPs and CSs. Should work to proactively partner with these roles.
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Significant experience with EDC platforms and database design, including Medidata Rave and Oracle Clinical Inform. Reporting to the VP of Biometrics, the Director/Sr. Director, Clinical Data Management is responsible for all clinical data management activities related to the effective planning and timely delivery of complete, high quality and reliable clinical trial data.
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The Real World Evidence (RWE) lead provides clinical leadership for evidence generation activities, supporting the integration of RWE into Sarepta key strategic initiatives. The role functions in a company matrix team environment interacting with several key stakeholder groups including; Clinical Development, Pharmacovigilance, Regulatory Affairs, Quality Assurance, Manufacturing, Commercial, Medical Affairs, Research and Legal.
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Highly competent in clinical data management, various EDC systems, CDASH/CDISC standards and medical coding dictionaries. Liaises with various internal and external groups (Clinical Development, Clinical Operations, Statistics, Statistical Programming, Pharmacovigilance, and external vendors including CROs) for the implementation of data management activities needed for clinical studies within his/her platform.
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A minimum of one-year experience in landscape installation and maintenance, including primary turf maintenance and snow removal techniques required.
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Build and maintain strong collaborative relationships with various key partnering functions, e.g. GI Drug Discovery Unit (GI DDU), GI Therapeutic Area Unit (GI² TAU), Clinical Science, Clinical Biomarker, Quantitative Science, and other functions and teams.
$205,100 - $322,300 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Full-time/Part-time Licensed Independent Clinical Social Worker (LICSW) Needed at Tranquil Minds Wellness in Cambridge, MA. Minimum 1 year of clinical experience, focusing on substance abuse therapy.
$80,000 - $100,000 a yearPart-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Title:Clinical Data Management Study LeadCompany:Ipsen Bioscience, Inc. Job Description:Clinical Data Management Study LeadSummary/Purpose of the Position:The Clinical Data Management (CDM) Study Lead defines, implements, and monitors the Data Management strategy for one or more clinical studies in Ipsen portfolio.
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The Opportunity: As Clinical Project Associate, you will be accountable for providing clinical trial coordination support, along with implementing operational plans in accordance with regulatory guidelines and ICH/GCP standards.
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Appropriate certification required: DESE School Social Worker License and Clinical Licensure (LMHC, LCSW, LICSW) The Social Worker will support Summer Academic program staff in the delivery of social emotional learning through modeling, coaching, and consultation.
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Lead statistician on multiple complex projects regarding Non-Clinical Efficacy and Safety (NCES) related Research activities with minimal direction from group head. The Non-Clinical Efficacy and Safety (NCES) team, within the Global Biostatistics and Programming Department of Sanofi R&D, contributes to reliability, scientific quality and optimization of Projects/Programs support from "target identification" to "compounds in development” by providing appropriate non clinical statistical support for efficacy and safety internal or external studies for all R&D entities.
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licenses: RN, LPN
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Provide input from the data management perspective regarding the design of clinical trial protocols. Minimum of 8-10 years of experience in Clinical Data Management. Manage and supervise a team of Clinical Data Managers (CDMs.
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Identifies and cultivates thought leaders in order to gain their inputs on emerging science in drug and biomarker research, disease knowledge, and design of clinical development studies and programs.
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Title: clinical social worker in Cambridge, Raleigh, West Virginia
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