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Proficient knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations. Protocol and ICF development process with minimal guidance; including writing, reviewing, adjudication/resolution of cross functional comments and ensuring high clinical quality (collaboration with Medical Writing.
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ArsenalBio, a privately held programmable cell therapy company engineering advanced CAR T therapies for solid tumors, is seeking a talented Associate Director, Clinical Business Operations to work hybrid or remotely.
$207,000 a yearFull-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Reporting to the Executive Director who oversees NonClinical Development and Clinical Pharmacology, the Clinical Pharmacology Associate Director/Director will be mainly responsible to support pegozafermin clinical program.
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The Associate Director of Clinical Quality Assurance will be responsible for building the clinical quality assurance processes and providing quality oversight for the clinical programs and CRO throughout the development stages of antibody-based radiopharmaceuticals.
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Associate Director, Clinical Supply Chain Who We Are Olema Oncology is a clinical-stage biopharmaceutical company focused on the discovery, development and commercialization of targeted therapies for women’s cancers.
$195,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Lead Clinical Research Associate manages the design, execution, and monitoring of internal and external clinical studies, coordinates the development of operating procedures, coordinates in the development of standard procedures in executing experiments, evaluation, and documentation of results, and contributes to the development of clinical strategy for ADC products.
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The Associate Director, Clinical Development creates the overall program strategy for early development/first-in-human through life cycle management and developing and overseeing the execution of the clinical study portfolio designed to meet objectives of a novel platform in gene regulation.
$226,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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We're looking for independently driven and detail-oriented individuals to join our team in Clinical Operations. Support clinical growth and innovation through evaluation of market- and clinical best practices, translating these insights into recommendations to inform our roadmap.
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As the Associate Director of Clinical Supply Chain reporting to the Senior Director, Clinical Supply Chain, you will plan, create, implement, build, and optimize the clinical supply chain to ensure uninterrupted and timely clinical drug supply for Olema’s clinical programs.
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Represent and provide clinical pharmacology expertise and leadership at cross-functional development project team, clinical subteam, study team, partnering with clinical research, biometrics, project management, clinical operations, drug metabolism, biology/biomarkers, toxicology etc.
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Reporting to the Executive Director, CDM, the Associate Director, CDM will be a highly motivated, quality-focused individual who can work collaboratively in a fast-paced, cross-functional team environment, and will manage data management activities across multiple studies from study start-up through study closure in support of clinical trial objectives and corporate goals.
$202,000 a yearFull-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Health Sciences /Clinical X/ In Residence- Assistant/Associate/Full Professor. The Department of Dermatology at the University of California, San Francisco is seeking outstanding applicants for a full-time position as an Assistant, Associate, or Full Professor for our Surgical-Mohs division.
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The Sr. Clinical Trial Manager/Associate Director manages the operational activities of assigned clinical programs. Minimum eight years of experience in Clinical Operations, working with CROs and other vendors at all stages of development within the biopharma industry.
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The Clinical Research Associate will assist in the clinical execution and management of all aspects of assigned clinical studies. Title: Clinical Research Associate.
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As the Associate Director, Clinical Data Management (CDM), you will be is responsible for supporting the leadership of CDM across multiple drug development programs including the development and implementation of data standards based on CDASH/SDTM, CRO/FSP CDM oversight, developing CRO partnerships.
$231,000 a yearFull-timeExpandApply NowActive JobUpdated 9 days ago
Title: clinical associate in Brisbane, CA
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