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Job Title: Clinical Trial Manager. Plans and coordinates all operational activities required with the collection, delivery and analysis of biological specimens within a clinical trial.
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Only qualified Clinical Operations Manager candidates located in the Foster City, CA area will be considered due to the position requiring an onsite presence. Provides sample management expertise to the Study Management Teams (SMTs), Biomarker SubTeams (BSTs), and Clinical Pharmacology Subteams (CPST.
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Clinical Operations – Biomarker and Bioanalytical Operations. Outsourcing, Clinical Operations, and Data Management) to ensure efficient execution of the study biomarker strategy. You will work with and collaborate with Clinical Operations, Biomarker Sciences, Clinical Pharmacology and other cross-functional team members.
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Excellent employment opportunity for a Clinical Trials Manager in the Foster City area. Will work with and collaborate with Clinical Operations, Biomarker Sciences, Clinical Pharmacology and other cross-functional team members.
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FUNCTION: Clinical Operations – Biomarker and Bioanalytical Operations. Clinical Operations is responsible for the worldwide execution of all Phase I - IV clinical trials across all Gilead therapeutic areas.
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POSITION SUMMARY As the Trial Master File (TMF) Specialist, you will be responsible for the day-to-day management of TMF, including oversight of the review and approval of TMF documents and generation of reports to measure completeness, accuracy, and timeliness of the TMF. This role works very closely with Clinical Operations and other departments that have a contribution to the TMF for studies.
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Meets all requirements for Senior Clinical Trial Management Associate (Senior CTMA) grade 26 position with demonstrable proficiency. PharmD / PhD with 2+ years’ relevant clinical or related experience in life sciences.
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Establishes strong cross-functional relationships and exhibits strong leadership skills with counterparts in other functional teams (e.g., Biomarker Sciences, Vendor Outsourcing, Clinical Operations, and Data Management) to ensure efficient execution of the study biomarker strategy.
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Licensed Clinical Drug and Alcohol Counselor (LCADC) is preferred. Preferred: Licensed Clinical Social Worker (LCSW), Licensed Psychologist (LP), Licensed ProfessionalCounselor (LPC), or Registered Nurse is required.
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Thorough knowledge of Food & Drug Administration (FDA), European Medicines Agency (EMA), and other applicable national regulations, International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) guidelines and Good Clinical Practice (GCP) governing the conduct of clinical studies.
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We are seeking a Senior Clinical Trial Specialist to assist in the execution of Clinical Trials. JOB TITLE: Senior Clinical Trial Specialist. Monitor progress of studies, help identify study related trends/issues and work with Clinical Trial Managers (CTM) to implement corrective actions when necessary.
$100,000 - $165,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The Quality Systems Manager is an advanced technical resource in the principles and application of quality systems and compliance. Sr. Quality Systems Manager. Our incredibly talented team of engineers, innovators, and industry leaders bring years of experience from the top healthcare companies in the world, including: Intuitive, Auris, Stryker, Johnson & Johnson, Boston Scientific, Verb Surgical, Mako, Think Surgical, Medrobotics, and Hansen.
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The Clinical Data Manager will be responsible for daily data management tasks for all phases of clinical trials including CRO/vendor oversight and support other functional areas such as clinical operations, statistical programming, and biostatistics.
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As the Corporate Accounting Manager you will work closely with a variety of team members in Accounting & Finance, Property Management, Asset Management, Resident Services, Development as well as the executive team at MidPen. Success in the role will be measured by the ability maintain and balance the technical aspects of the role, support and create internal controls and policy of the organization, demonstrate strong leadership to direct team members and across the organization.
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Previous experience working in a matrixed environment to implement flow cytometry assay development and validation to support clinical trials. In this vital role you will design, develop and implement clinical biomarker assays employing innovative flow cytometry methods and techniques to support our drug development efforts.
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Title: clinical trial manager Company: Thrive Events in Burlingame, CA
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