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We work with companies funded by the best investors including Sequoia Capital, Lightspeed Ventures, Tiger Global Management, A16Z, Accel, DFJ, and more. You will be selling the best outbound tool on the market to SMB accounts (early stage startups, marketing companies, and professional service companies pre their first sales hire.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Key ResponsibilitiesStrategy and Execution:Uses an understanding of disease biology, the drug development process (particularly cross-functional connectivity), and relevant late-stage challenges (e.g., trends in disease area therapeutic advances, and evolving regulatory, patient advocacy and market access environments) to create a vision for each asset, then design and execute effective development programs in support of the overall R&D portfolio goals.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Uses an understanding of disease biology, the drug development process (particularly cross-functional connectivity), and relevant late-stage challenges (e.g., trends in disease area therapeutic advances, and evolving regulatory, patient advocacy and market access environments) to create a vision for each asset, then design and execute effective development programs in support of the overall R&D portfolio goals.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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As a staff member of CMC Regulatory Affairs Department of Japan Development Division, a person in charge who is willing to contribute in CMC Regulatory Affairs (RA) tasks from initial stage of new drug development to NDA filing and the approval, addition of dosage form, and change controls.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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As GMP QA Associate Director you will be an important part of the global GMP QA team to ensure compliance to industry standards and regulations. In this position, the Quality Assurance (QA) Associate Director will set the quality direction for Genmab’s Late-Stage Development products.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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ADC Therapeutics (NYSE: ADCT) is a global, rapidly growing commercial-stage biotechnology company that is improving the lives of cancer patients with its next-generation, targeted antibody drug conjugates (ADCs) for patients.
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Design/Develop/maintain the batch programs in IBM Mainframe using COBOL, JCL. Conduct project execution in a global delivery model and contribute to every stage of the software development cycle such as analysis, design, development, maintenance of applications and systems.
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Extensive early/late stage drug development experience ideally including time in role such as a Global Project Leader at Sr. Director level or equivalent preferred. The Executive Director, Global Clinical Operations Study Management Group Head has leadership and overall strategic oversight of study management and delivery for all therapeutic areas.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Executive Director, Global Clinical Operations Study Management Group Head. The role reports into the Global Clinical Operations VP and is accountable for ensuring the clinical trial portfolio and submissions are delivered to time, quality, and cost.
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About the Department Our East Coast Global Development Hub brings together the best minds in life science innovation with facilities in Lexington, MA and Plainsboro, NJ. We support programs from early research through late-stage clinical development.
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Safe and timely execution of Phase I studies; close collaboration with internal and external clinical study support staff and scientists (including discovery research, biostatistics, drug metabolism, modeling and simulation, regulatory affairs, and global clinical trials operations.
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