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This position independently manages relationships with internal (CSPV, Regulatory, Clinical, Medical Affairs, HEOR and other stakeholders to ensure expectations are clearly defined and met across participating teams) and external stakeholders.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Education Qualifications (from an accredited college or university) - Bachelor's Degree (preferred in Life Sciences) with relevant clinical development experience required Experience Qualifications - 2 or More Years with Bachelor of Science required - Experience considered relevant includes clinical or basic research in a Pharmaceutical company, a Medical device/Diagnostic company, Academic Research Organization (ARO) or Contract Research Organization (CRO.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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This role will also work closely with global and regional (Osaka, Japan [SHQ]; Florham Park, New Jersey [SI]; and London, England [SEU/SBV]) cross-functional team members including Medical Affairs, HEOR, Clinical Development, Regulatory, Market Access, Commercial teams and external collaborators/vendors to lead and conceptualize research questions, propose study designs, identify appropriate databases, write and review protocols, oversee data analyses, reports, presentations, and publications.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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This position entails effectively interfacing and collaborating with key stakeholders including: Ethics & Compliance, Legal, Medical Affairs, Clinical Research, Oncology Patient Advocacy, US Pharmas Grant Office (NOGE), and Finance.
Full-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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The Associate Director, for the Oncology Office of Grants and Education (OGE), is responsible for supporting the Head of OGE with the development of medical education plans, assist in providing direction and oversight for all continuing medical education initiatives, and implementing Novartis policies and procedures in alignment with external regulations.
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The Associate Director, for the Oncology Office of Grants and Education (OGE), is responsible for supporting the Head of OGE with the development of medical education plans, assist in providing direction and oversight for all continuing medical education initiatives, and implementing client policies and procedures in alignment with external regulations.
Full-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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The Associate Director, Clinical Records & Information Management will partner with cross functional teams as well as Clinical Research Organization (CRO and Functional Service Provider (FSP) to ensure timely and quality delivery of the TMF. This role is a member of the Clinical Records leadership team to ensure optimum implementation of the TMF technical capabilities and oversight of standardization, training, quality, and timely clinical trial documentation across the clinical program.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Qualifications:+ 3+ years of experience in Clinical Research supporting Clinical Trial Managers/Clinical Research Manager on studies + eTMF Experience (Experience maintaining the eTMF (file, upload, scan, QC all study documents such as 1572, financial disclosures, informed consents, CV’s (etc.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Possesses proficient scientific expertise to propose, design, and execute clinical research and development studies for early and/or late stage assets; able to conceive and communicate strategy proposals well-grounded in supporting literature.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The Associate Director, Clinical Scientist leads in the development, evaluation, planning and execution of hematology oncology clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program.
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About CRN Founded in 2002, Clinical Resource Network (CRN), a division of Solomon Page, provides clinical research and talent solutions for pharmaceutical, biotech, and medical device companies.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Requirements Excellent communication skills (interpersonal, written, verbal) Basic computer skills to include Word, Excel, as well as proprietary applications unique to the clinical research industry (such as Study Manager)Organized.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Coordinates PE activities within Novartis, Global Business Solutions (GBS) and vendors under supervision of a PE lead Manages multiple projects to collect information from patients about their disease/condition and to gather patient input into clinical trial design and treatment goals via social media listening, online bulletin boards, online surveys, online patient panels, desk-side research, etc.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Experience in clinical research and development, or medical affairs in Hematology/Oncology preferredOperational experience across a range of commercial and/or R&D roles a plusMust demonstrate ability to lead strategically, drive performance, build alignment, inform, negotiate and collaborate.
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Founded in 2002, Clinical Resource Network (CRN), a division of Solomon Page, provides clinical research and talent solutions for pharmaceutical, biotech, and medical device companies.
ExpandApply NowActive JobUpdated 10 days ago
clinical research associate jobs in Morristown, NJ
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