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Purpose The Home Study and Post Release Services Caseworker (HS and PRS Caseworker) in Lancaster, PA will provide collaborative home study services to Unaccompanied Immigrant Children’s sponsors to support the safe and timely release of Unaccompanied Children (UC) from Federal care.
$52,800 - $66,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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This role is responsible for overseeing all aspects of drug safety study operational activities from study start up to close out. Oversee Drug Safety Study Team Leads activities including review of study protocols, case report forms, Investigator Brochures and participation on IND Annual Reports in support of the Drug Safety Physician.
$210,000 - $297,500 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Oversight and review of drug safety operations practices. Ensure case reports are appropriately scheduled in Argus based on regulatory reporting matrix in conjunction with Drug Safety submissions. Develop and/or update SOPs, processes and practices for SAE and other safety data collection in accordance with drug safety and pharmacovigilance regulations, ICH standards and guidelines as appropriate to ensure timely and compliance submissions to worldwide regulatory agencies.
$210,000 - $297,500 a yearExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Purpose: The Home Study and Post Release Services Caseworker (HS and PRS Caseworker) will provide collaborative home study services to Unaccompanied Immigrant Children’s sponsors to support the safe and timely release of Unaccompanied Children (UC) from Federal care.
$52,800 - $66,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Complete reports within 10 days of receiving Home Study referral with assessment information and findings. Responsibilities: Home Study Conduct in-person home visits to interview and provide psychoeducation to Sponsors.
$52,800 - $66,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Serves as Study Coordinator for pharmaceutical trials. Supports regulatory staff submission of study protocols and amendments, consent forms, and recruiting materials to the Institutional Review Board and department for approval with oversight from supervisor.
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Wages under this position are paid from Work Study awards administered by the CSN Financial Aid Department. Student's cannot work another part-time position within NSHE at the same time they are employed as a CSN College Work Study student.
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Based out of Newark, NJ area, The Travel Clinical Research Coordinator primary responsibilities are to utilize Good Clinical Practices (GCP) in the process of screening, as well as enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.
ExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Additionally, a large of component of this position requires development of computational biology course materials and to teach our graduate students wet-lab study design for NGS studies and computational analysis.
$85,000 - $92,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Senior Registry Specialist/Study Project Manager will lead and manage the daily activities for one or more AtriCure sponsored Registries and Registry projects in support of strategic real-world evidence (RWE) initiatives to meet company goals.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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The Senior Scientist functions as a study director to manage the design, execution, analysis, and reporting of pre-clinical discovery research studies across various therapeutic areas. The Senior Scientist is expected to deploy their scientific domain expertise to 1) lead communications with sponsors, 2) interface with business development teams, 3) engage laboratory staff and IACUC, and 4) coordinate with project management and data analysis teammates to manage all aspects of studies from initial pre-clinical study design to final report.
Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Maintain Registry Clinicaltrials.gov updates and study-level central Institutional Review Board (IRB) approvals. Facilitate the preparation of project and study newsletters, correspondence, study documents, and progress reports.
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The Statistical Analyst B will use SAS, STATA, SQL, and/or R programming skills to develop and execute analysis plans, conduct sample size calculations, assist with database development, and develop and generate reports and projections to support study management and overall operations.
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Effectiveness and College Relations is seeking a work-study student to join our team as a Social Media AssistantThe Social Media Assistant will support the Web Marketing and Communications Coordinator with promoting LCC events, resources, and academic information.
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Contribute to the build and test of Real-World Evidence databases by defining study requirements specifications such as data validation specifications and participating in User Acceptance Testing (UAT) as needed.
$107,064 - $167,911 a yearExpandApply NowActive JobUpdated Today
study job Company: Focusgroupjobs
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