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This individual will work closely with leaders across Research, Early Clinical Development, Computational Sciences, and Development Sciences in gRED, and Product Development, Medical Affairs and Global Product Strategy (GPS), Spark, FMI as well as global functions across the Roche organization to contribute to strategies to discover and develop impactful therapies that provide transformative benefit for patients.
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Interact with document authors, contributors, and reviewers (including members of Biometrics, Clinical Operations, Clinical Development, Project Management, CMC, Drug Safety, and Regulatory Affairs) to acquire necessary input into documents.
$180,000 - $250,000 a yearFull-timeExpandApply NowActive JobUpdated 29 days ago - UpvoteDownvoteShare Job
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Represent Global Regulatory Affairs on the Global Artwork Team; help develop, review, and approve global package artwork in close collaboration with Supply Chain, Quality Assurance, and International Regulatory Affairs colleagues.
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The Quality Control Specialist will join our Quality team to be a key player in all scientific and documentation aspects of product development, release, stability, and investigations in support of maintaining and improving processes within the CRISPRevolution Production Team at Synthego.
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The Learning Specialist delivers instructor-led, classroom, webinar, one-on-one and web-based training to both new and existing SRG employees, with an emphasis on SRG sales, customer service, and leadership development.
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As our Senior Director, Clinical Regulatory Affairs, you’ll lead and drive Arcellx’s clinical regulatory approval strategy and implementation and oversee post-approval regulatory requirements.
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Meet is partnering with a late stage pediatric rare disease startup looking for a high-level Regulatory Affairs professional to join their team. This position will be reporting into the SVP of Regulatory Affairs and will be supporting Clinical Regulatory and Regulatory CMC functions.
$240,000 - $280,000 a yearFull-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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QUALIFICATIONS:At least 2 years of relevant work experience as a Community Health Worker, Peer Support Specialist, Medical Assistant, or similar roleHigh school graduate or GED required. The Care Specialist works in patient’s homes and community 90% of the time and virtually the other 10% to deliver chronic care management to high complexity patients.
$22 - $24 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Office of the Vice Provost for Student Affairs. Business Affairs: University IT (UIT), Redwood City, California, United States. Experience with cloud data warehousing solutions, such as Snowflake, AWS RedShift, a plus.
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IT Support Specialist. MDM solutions (Jamf & Microsoft InTune) Experience managing and supporting SaaS applications such as Google Workspace, Zoom, Okta, Slack, and Office 365. Collaboration tools (Zoom, RingCentral, Slack.
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But working at Bristol Myers Squibb is anything but usual.
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The candidate will be responsible for leading the Regulatory Affairs function and will oversee and direct the strategic planning and execution of clinical regulatory activities essential for initiating and conducting clinical trials and securing marketing authorization.
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Child Life Specialist Certificate within 12 months of hire. Current Child Life Specialist certification preferred. Ensures each childs program is consistent with The Joint Commission and other regulatory requirements.
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ArsenalBio, a privately held, clinical-stage programmable cell therapy company engineering advanced CAR T therapies for solid tumors, is seeking a talented Facilities Lead to work onsite based in our South San Francisco office.
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Bachelors or advanced degree in a scientific discipline, with a minimum of 10 years of experience working in drug development in the biopharmaceutical industry and at least 8 years of experience in Regulatory Affairs; immunology or rare disease/ orphan drug development experience desirable.
$225,000 - $255,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago
affairs job Title: regulatory affairs specialist Company: Parexel in San Mateo, CA
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