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With a combination-focused pipeline that exploits the power of six scientific platforms (Immuno-Oncology, Tumor Drivers and Resistance, DNA Damage Response, Antibody-drug Conjugates, Cell Therapy and Epigenetics) to help address unmet clinical needs in a host of hematological cancers, we are motivated by a dedication to the scientific discovery and collaboration that will one day help eliminate cancer as a cause of death.
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Podcast episodes are pre-recorded 60 minute interviews with a blood cancer expert about their open clinical trials. 3+ years of experience in a health-related setting working with patients: health coach, health educator, public health, nursing, social work, psychology, nutrition, etc.
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We are seeking a Clinical Research Coordinator to join the Division of Digestive & Liver Disease within the Department of Medicine at CUIMC. This role will be instrumental in coordinating the research activities of multiple ongoing projects, including NIH/NCI grant-funded studies and industry-sponsored clinical trials.
$75,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Unique International Collaborative Team for MPNs: The MPD Clinical Consortium is the only large, multi-centered, international academic collaboration involving 45 clinical centers within the USA and 7 other countries that is focused on developing scientifically based, hypothesis testing clinical trials for the treatment of MPN patients.
$98,827 a yearExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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As the Director of Trial Master File Operations, you will be responsible for leading the TMF (Trial Master File) operations function for clinical trials across Eikon Therapeutics. The successful candidate will be a strong leader with excellent communication and collaboration skills, and experience in managing TMFs for clinical trials.
$218,500 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Advancing the health and wellness of society through clinical trials, Flourish Research is one of the largest integrated clinical research site companies in the US, with best-in-class sites who have a strong brand and track-record of recruiting and retaining a highly diversified patient populations in the therapeutic areas of cardiology, metabolic disorders/renal, CNS, pulmonology, and vaccines.
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The job purpose and scope of the Structural Heart Clinical Lead Specialist (CLS) is an integrated part of clinical trials and commercial sales in collaboration with the Regional Sales Directors and the Clinical Lead Manager (CLM.
$145,300 a yearFull-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Collaborates with cross functional teams (Biostatistics, Clinical Operations, Data Management, Regulatory, PK/ADME, Pharmacovigilance, Commercial) during design, execution, and reporting of early-stage clinical trials.
$264,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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CPD scientists focus on developing safe, economical, sustainable, and robust processes to support clinical trials and the launch of new medicines across various drug modalities including small molecules, peptides, oligonucleotides, and antibody drug conjugates.
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This role involves negotiating complex standalone commercial transactions that advance technologies through clinical trials and toward FDA regulatory approval. Requirements:Juris Doctor (JD) degree from an accredited law school.
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Interpret clinic schedule and protocol into a resource that can be used to identify the date/time to compound/prepare and dispense IP for clinical trials. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials.
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Prior experience in providing MSL-level support to products or devices in endocrinology and/or rare disease, including KOL development, investigator-initiated clinical trials, publications and educational programs, highly preferred.
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Responsible for oversight of all components of the grants cycle, including pre-award budget development, post-award monitoring, program sub-contract management, and grant closeout procedures.
$97,790 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Worked on drug trials that use a biomarker to select patients into the trial, include but not limited to, understand clinical trial assay (CTA) requirements with diagnostic partners, sample testing/shipping regulations in different countries, and CDx development requirements.
Full-timeRemoteExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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A large medical device company located in Irvine, CA is looking for a Clinical Study Associate to support the planning, executing, and management of clinical trials. Coordinate and manage logistics for clinical trials.
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