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Risk Management: Identify and mitigate risks associated with clinical trials to ensure patient safety and data integrity. Key Responsibilities:- Study Management: Lead and manage clinical trials from initiation to close-out, ensuring adherence to timelines, budgets, and quality standards.
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This will be an on-site position in the location listed below with a large CRO Job DescriptionSummary: A typical Research Assistant performs a variety of administrative tasks in support of clinical trials and assists in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies.
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Summary: A typical Research Assistant performs a variety of administrative tasks in support of clinical trials and assists in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies.
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Job Description - Clinical Research Assistant in Gulfport, MS Perform a variety of administrative tasks in support of clinical trials and assists in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies.
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Job Title: Clinical Research AssistantJob DescriptionSummary: A typical Research Assistant performs a variety of administrative tasks in support of clinical trials and assists in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies.
$20 - $30 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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This role involves managing clinical research studies in compliance with operating procedures, ensuring the integrity and quality of clinical trial data through accurate data collection and reporting.
$40 - $45 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Input research study data into trial Electronic Data Capture (EDC) system, maintaining quality control for content, accuracy, and completeness. Input visit data into Clinical Trial Management System (CTMS) to track patient visits and procedures completed against the study budget.
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Basic knowledge of clinical trials. Research queries and variances, and provide feedback to the site data collector. Experience with Patient recruitment, EDC data entry/query resolution required.
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Experience with Patient recruitment, EDC data entry/query resolution, Clinical Research Assistant~ Multiple Locations Available! At Actalent, diversity and inclusion are a bridge towards the equity and success of our people.
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Job Description - Clinical Research Assistant. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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Actalent is a global leader in engineering and sciences services and talent solutions. In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules.
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Great experience with Clinical Trials and data analytics. Support the Global Safety Officer (GSO) in the conduct of quality safety assessment and risk management processes and activities for an assigned set of products through the product's lifestyle.
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Summary: A typical Clinical Research Assistant performs a variety of administrative tasks in support of clinical trials and assists in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies.
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We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. Building a culture of care, engagement, and recognition with clear outcomes.
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Compile, collate and submit study information within established deadlines. Verify and/or correct research study information on source documents. Schedule subject visits and generate appropriate reports and documents for research subjects prior to visits.
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data quality clinical trials jobs Company: Actalent
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