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Experience in Good Clinical Practice (GCP) and regulatory compliance guidelines for clinical trials. In this exciting role as the Senior Field Clinical Research Specialist, you will be responsible for clinical trial site management, case coverage, and clinical trial data tracking.
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Clinic Research Coordinator II The Clinical Research Coordinator II , will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor.
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The Clinical Sales Specialist (CSS) - Ophthalmology will provide technical sales support for all Medical products. Clinical Sales Specialist - Ophthalmology. Leica Microsystems is one of the market leaders in the fields of microscopy, imaging, and analysis.
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Collaborate cross-functionally with Clinical Operations, Manufacturing, Regulatory Affairs, and Quality Assurance to forecast, plan, and execute IMP supply plans including IMP utilization, labeling and packaging, inventory control, and depot management for assigned clinical studies.
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We are currently enrolling two Phase 2 clinical trials for patients with SM and a global Phase 3 trial for GIST patients. Rare diseases/oncology clinical trials. The successful candidate will be responsible for supporting all aspects of clinical trial management for a novel precision kinase inhibitor in rare disease.
$125,000 - $175,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Experienced Clinical Research Associates- a ccelerate your hematology/oncology career by joining Medpace today! Candidates must have at minimum a Bachelor's degree in a health or science related field, minimum one year of clinical research experience or relevant direct industry experience (e.g., CRC), ability to travel nationwide, must be detail-oriented, strong time management, and communication skills.
$90,000 - $140,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Experience in rare disease, pediatric, and/or complex clinical trials preferred. You will be responsible for the successful execution of clinical trials from protocol finalization through closeout.
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This individual is the subject matter expert in GCP, is responsible for developing standards and partnering with Clinical Operations, Regulatory, Biostatistics, Safety, Medical Affairs, and other functions to establish and document risk based GCP processes and procedures.
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As an Rheumatology Clinical Account Specialist (CAS) you will be responsible for driving demand for the assigned product, CIMZIA® (certolizumab pegol), by reinforcing the clinical features of the product and UCB value within an assigned territory; engaging and building relationships with clinical decision makers and office support staff to create the best experiences for patients living with severe immunologic diseases who are treated in the home care setting.
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Knowledge of industry-standard data analysis and reporting software, such as SAS, SQL and/or Oracle Clinical. Proficiency in electronic data capture (EDC) systems and clinical data management software.
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Wage: Between $84 - $131 an hour Are you a licensed Clinical Social Worker looking to launch a private practice, or grow your existing practice? Wage: Between $84 - $131 an hour Are you a licensed Clinical Social Worker looking to launch a private practice, or grow your existing practice.
$131 a dayRemoteExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Manage a region of 7+/- Biomarker Integration Managers and Hospital System Executives (HSEs) and clinical educators to grow overall test volumes. Minimum 2 years of clinical demand generation focused sales activity in the hospital setting.
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Verifies information with clinical research nurse and/or principal investigator. Independently or in conjunction with other clinical research staff and/or research nurse, recruits and enrolls research subjects onto clinical research projects according to study protocols.
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Lumenis is looking for a Per Diem Clinical Application Specialist. Maintain open communication with the Clinical Application & Training Manager and sales staff. Lumenis is seeking Per Diem Clinical Applications Specialists to provide training and professional support on multiple aesthetic and vision device platforms.
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Responsible/Accountable for the management of global oversight monitoring for the Company sponsored clinical studies or programs, ensuring monitoring oversight quality is following SOPs, regulations and ICH/GCP guidelines.
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Title: clinical trials Company: Parexel in Newton, MA
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