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Manage all study specific data management activities such as CRF design, CRF flow definition, DMP preparation, database setup and validation, data entry, data review, discrepancy management, data review, CRF/DCF tracking, data reporting, data coding, database lock, project documentation, transfer to biostatistics for analysis, electronic submission and archiving.
$110,000 - $140,000 a yearFull-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Perform lab testing to demonstrate the ability of the product/device to function as intended under study director/management supervision. Precisely follow company tissue requests, study designs, protocols and SOPs for the complete processing of tissue based products with minimal supervision.
Full-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Participate in the programming processes from study start up to database lock. Works collaboratively to meet study deliverables and timelines for statistical data analysis and reporting.
ExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Provides guidance to study team on all aspects of statistical activities; collaborates closely with data manager to ensure high quality data. Protocol Development, Case Report Form (CRF; review), Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Leads statistical activities for complex studies including study design, protocol development, CRF review, SAP development, analysis files development, statistical analysis accuracy validation, results interpretation and CSR input and review.
ExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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This includes, but is not limited to: identifying optimal study designs, defining data analysis strategies, implementing statistical analysis plans, interpreting the resulting findings and crafting and communicating key messages to internal audiences and selected key external stakeholders.
Full-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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Assist in the conduct of clinical trials as specified by the study protocol under the supervision of designated Principal Investigator and departmental management. Perform data entry and data review to ensure study quality.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Partner with key functional key stakeholders to capture all operational details of ISS, RWE, study data milestones, and budget specific to all studies defined in the Medical plan. Partner with Clinical Study Operations to ensure a robust clinical feasibility process to ensure alliance budgets are accurate early in the clinical development, allowing for smooth transitions into the alliance governance process.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Biostatistician (2 x openings) in Somerset, NJ : Write/review clinical research protocol, SAP and study report for clinical trials projects; develop and validate statistical models and SAS programs for analysis, management and reporting of clinical trials data, generate and validate safety and efficacy TLGs, analysis datasets (SDTM, ADaM) and clinical trial reports.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Work with clinical study teams to evaluate outsourcing needs for global clinical trials and assist in developing specifications for contracted deliverables. Work with clinical study team to monitor supplier’s compliance with contract terms, conditions, commitments and notifications.
$104,400 - $195,400 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Represents Biostatistics as a member of cross functional teams, accountable for statistical aspects of statistical design, study setup, execution, analysis and reporting of clinicals. This role leads the protocol statistical section development, study setup, execution, analysis, and reporting of clinical trials, and interacts with cross-functional teams.
$140,000 - $200,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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The path to becoming a Financial Professional begins with the Pre-Contract CDP Affiliate phase, during which you will study towards obtaining the required FINRA and resident state licenses, with the cost of fees and exam study materials from approved vendors covered by the Company.
$50,000 - $75,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Bachelors Degree (BA/BS) Accounting, Finance, or other financial area of study - Required. Specialized Knowledge - JD Edwards, Proficient in Excel. Ability to cross-train and learn additional areas of responsibility within Trade Finance, such as rebates, contract administration, etc.
Full-timeExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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Collaborate with clinical, regulatory, and quality team members to ensure department/study activities comply with FDA regulations, guidelines, and principles of ICH GCP and company SOPs. Experience with all aspects of trial and site startup, vendor selection and management, study management, and monitoring.
Full-timeExpandApply NowActive JobUpdated 4 months ago - UpvoteDownvoteShare Job
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8+ years of professional experience and a Bachelor of Arts/Science or equivalent degree in computer science or related area of study; without a degree, three additional years of relevant professional experience (11+ years in total.
ExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Acts as the lead programmer or project lead on studies of significant complexity, working directly with project team leaders and client representatives to conduct team meetings, develop and maintain project timelines, assess and forecast resources, and monitor study budgets.
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toxicology study jobs in Bridgewater, NJ
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