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The R&D Sourcing and Contracting Associate will be responsible for assistance in the pre-clinical / research, clinical sourcing in support of Gilead’s global Phase I-IV clinical trials, and other ad hoc projects in the Vendor Outsourcing department.
$50 - $56 an hourExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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As a team member you will be a key contributor to a fast-paced team responsible for the management of drug development vendors.
$70 - $80 an hourExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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You will attend trials in district courts across the country, as well as briefings and oral hearings at thePTAB, as well as represent clients before the Federal Circuit and the International Trade Commission.
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Experience in scientific research, clinical trials desirable. personnel in Global Medical Affairs, across Medical Affairs, Commercial, Development Business Operations, Global Safety and Medical Communication.
ExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The R&D Sourcing and Contracting Associate will be responsible for assistance in the pre-clinical / research, clinical sourcing in support of global Phase I-IV clinical trials, and other ad hoc projects in the Vendor Outsourcing department.
$50 - $56 an hourExpandApply NowActive JobUpdated 26 days ago - UpvoteDownvoteShare Job
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The R&D Sourcing and Contracting Associate will be responsible for assistance in the pre-clinical / research, clinical sourcing in support of company’s global Phase I-IV clinical trials, and other ad hoc projects in the Vendor Outsourcing department.
ExpandApply NowActive JobUpdated 26 days ago - UpvoteDownvoteShare Job
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S global Phase I-IV clinical trials, and other ad hoc projects in the Vendor Outsourcing department. Assists other Vendor Outsourcing staff in resolving moderately complex issues relating to contract negotiation or management and with the support of internal customers and the Legal department, assists in the contract negotiation process, especially with less complex, or low value contracts.
ExpandApply NowActive JobUpdated 26 days ago - UpvoteDownvoteShare Job
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Our client is a pre-IPO biotech company in South San Francisco that has raised over $300M in financing and has a several drugs in late-stage clinical trials. Our client is a pre-IPO biotech company in South San Francisco that has raised over $300M in financing and has a several drugs in late-stage clinical trials.
$215,000 - $235,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Oversee multiple global clinical trials at a time through pre-study visits, close out visits, monitoring visits, and initiation visits. Oversee multiple global clinical trials at a time through pre-study visits, close out visits, monitoring visits, and initiation visits.
ExpandApply NowActive JobUpdated 6+ months ago - UpvoteDownvoteShare Job
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Provide strong cross-functional leadership for global filings including authoring and reviewing sections of IND, CTA, NDA, MAA, and other global submission documents in support of clinical trials and marketing applications, as well as their amendments, in conformance with local regulatory requirements.
$250ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Facilitating accurate and timely payments to investigators participating in clinical trials is essential. Facilitating accurate and timely payments to investigators participating in clinical trials is essential.
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Most trials don't require much effort and will be located near you. Potentially get paid to access the most cutting edge medicines combating your disease. Whether you are healthy, or have a specific illness, we'll connect you with the right trial.
Part-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Ability to manage delegated aspects of assigned clinical trials. Ability to manage delegated aspects of assigned clinical trials. Ability to identify potential risks that may impact the studies, e.g., study data, ethical conduct and adherence to ICH guidelines and provides risk mitigation solution.
RemoteExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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SCIENCE- Guardant Health, Inc. in Redwood City, CA seeks Clinical Trial Manager: Approve study-specific documentation such as diagnostic protocols, trial monitoring plans, & deviation management plans that align with clinical study protocol & regulatory requirements for medical device trials.
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Prior solid tumor oncology disease/drug experience in late-stage drug development and understands registrational trials is strongly preferred. Proficient user of MS Office suite (e.g., PowerPoint, Word, Excel, Project), experience using electronic document management systems, document review tools and expertise in standard project management software (Smartsheets) required.
ExpandApply NowActive JobUpdated 2 days ago
trials job in Foster City, CA
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