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Job Overview: Seeking a Clinical Research Scientist with strong expertise in Oncology, Immunology, or Immuno-oncology to lead the implementation, planning, and execution of clinical trial activities, collaborating with various stakeholders and driving Clinical Development strategy in a fast-paced, collaborative environment.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Monitor fund activities on an ongoing basis and reconcile fund balances upon clinical trial closure by working with MGH Cardiology financial leaders and Grant Accounting to ensure timely account closure.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Ensure the activities described in the Data Management Plan (DMP) are executed in accordance with the DMP, including data acquisition, data transfer, data reconciliation and review, medical coding, data extract and rolling data freeze, data lock and database lock.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Author, review, and approve SOPs and policies related to QC activities, including management of stability data, expiry assignments, and product specifications. This position reports to the Associate Director Quality Product Testing and will oversee compliance of GMP activities for assigned Contract Testing Laboratories (CTL)/Contract Manufacturing Organizations (CMO) as it relates to QC testing of ImmunoGen products.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Draft, review, revise or provide input to GCP/GLP SOPs to assess consistency and compliance with regulatory requirements/internal standards. Work closely with GCP/GLP functional groups to ensure/coordinate appropriate and complete resolution of findings/non-compliances, deviations, investigations, CAPAs in a timely manner, including oversight and approval of all abovementioned activities, as necessary.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Perform high quality clinical data review and identify clinical data insights through ongoing patient level review and trends analysis, thereby supporting for example Interim Analysis, Database and Post Lock activities and resolution of scientific & medical issues throughout the study lifecycle.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Review of master and executed batch documentation and assurance of compliant release of drug substance and drug product batches to support commercial supply activities and any development and validation requirements.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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In collaboration with PI and manager, develops and implements new research protocols including design, data collection systems, and institutional review board (IRB) approval. Independently coordinates all activities of clinical trials and clinical research including but not limited to supervising the daily activities of research assistants, implementing, and maintaining quality assurance procedures, designing research protocols, and overseeing and conducting study enrollment and activities.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Assists the physician as follows, but not limited to Utilization Review, Quality Assurance, Program Evaluation, Infection Control, Safety Committee activities. Ensure completion of all required documentation of patient care activities in accordance with TPR policy.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Collaborate and liaise with clinical sites to support overall clinical trial participant management, data review activities and facilitating issue resolution. Perform ongoing and timely clinical trial data review in the form of listings, tables, patient profiles and live clinical database.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Assist with clinical study activities such as study start up, investigator meetings, data review, etc. The range of tasks will include activities assigned by the Clinical Lead, Clinical Scientist and/or study physician, and may vary to some degree depending on the therapeutic area and trial-specific requirements.
InternExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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The Director of Planning and Program Development in Seattle, WA (Region 10), provides leadership and expert technical guidance to carry out the Region’s core functions related to grant and project development, which includes all state and local planning, and environmental compliance activities which support critical infrastructure investments.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Duties, responsibilities, and activities may change at any time with or without notice. Work in a Beautifully Remodeled Office Professional Growth & Stability Innovative Training Programs Benefits: 401(k) Dental insurance Health insurance Paid time off Vision insurance Duties and Responsibilities: May include all or part of the following but not limited to: Review menu prior to preparation of food.
$17 - $19 an hourExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Ensure that CDM documentation is filed into the Trial Master File (TMF) according to SOPs and the study plans; review CDM files for completeness and accuracy. We are seeking a Senior Manager to lead Clinical Data Management (CDM) activities for clinical studies or clinical program(s.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Familiarity with clinical trial design and analysis activities and basic knowledge of regulatory guidelines (FDA/CFR, ICH/GCP) Lead inspection activities for CDM and manage any findings to resolution.
ExpandApply NowActive JobUpdated 4 days ago
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