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Contribute to the writing of key study and regulatory documents (e.g. protocol, ICF, study manuals, briefing books) Proficient knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations.
$170,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Be compliant with infection control procedures and environmental safety protocol within a facility. Build a strong occupational therapy programEnhance clinical expertise, professional and management skills through interaction with managers, therapists and other professional staff, self-study, and other continuing education activities.
$50 - $55 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Work closely with functional partners (Data Management, Biostatistics, Regulatory, GCO) to ensure an integrated and strategic approach to flawless execution and systematic oversight of study protocol(s) in clinical development in close collaboration with key functional stakeholders.
$332,500 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Build a strong physical therapy program Enhance clinical expertise, professional and management skills through interaction with managers, therapists and other professional staff, self-study, and other continuing education activities.
$41.28 - $54.86 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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EXPERIENCE: One (1) year of research experience in subject recruitment, informed consent, understanding of IRB requirements, and following a research study protocol; OR a combination of education, training, and experience to equal five (5) years.
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Operating the 3T Siemens MRI scanner for research MRIs as outlined by the study protocol, and for clinical patients’ MRI. Work closely with research study groups to ensure success as outlined in the study design.
$45 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Possesses the knowledge and skills level to administer treadmill and ergometer protocols for a variety of stress tests which includes: monitor, record, and interpret EKG tracings for diagnostic purposes, determine appropriate testing protocol, recognize presence of permanent pace maker, calculate and record diagnostic parameters, monitor and evaluate patient tolerance to test including chest pain, and prepare study for physician interpretation.
$37 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Recruiting Department: MGH Cancer Ctr - Protocol. The Cancer Center Protocol Office (CCPO) provides essential support for clinical investigators and their patients through patient recruitment, regulatory compliance, data collection, financial organization, administrative support, and other vital services.
Full-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Provides Just-in-Time documentation and evidence of compliance, including Human Subjects Research (IRB) and Vertebrate Animal Research (IACUC) protocol approvals, Other Support pages, salary confirmations, and other information as needed.
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This role serves as the primary or backup medical monitor contact in study protocols to investigators and study sites team regarding protocol compliance issues and safety of the subjects enrolled, and is a critical member of the Clinical Development team within Unither Bioengineering.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Contributes to the establishment and maintenance of common formats and templates for key Biostatistics documentation (e.g., statistical section of protocol, standard CRF pages, Statistical Analysis Plans, Tables, Figures and Listings.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Studies protocol preparation and facilitation of study procedures, institutional review board application (IRB) and animal protocol (IACUC) preparation. This positions facilitates performance of clinical studies, including protocols preparation, preparation of study design, interacting with clinical teams and students, sampling processing, preparation of reports, publications and grants.
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This includes working with life sciences toxicologists, pathologists, non-clinical IT teams, CDO/CIOs for end to end trial management, protocol management, study data creation, reporting and SEND submissions.
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This role primarily focuses on supporting a clinical research trial titled "Enhancing Intensive Transdiagnostic Cognitive Behavioral Therapy for Veterans with PTSD and Anxiety Disorders," led by Dr. Ellen Teng, PhD. Job Duties:Conduct treatment protocol adherence and fidelity ratings for the intervention conditions evaluated in this study.
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Responsibilities Assists with the development and Institutional Review Board (IRB) submission of research protocol applications and consent forms on behalf of the study Principal. Performs quality control, research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring that Good Clinical Practices (GCP) are adhered to and communicating protocol deviations appropriately per Standard Operating Procedures (SOP), GCP, and applicable regulatory requirements.
Full-timeExpandApply NowActive JobUpdated 15 days ago
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