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The Senior/Executive Director may also work closely with global Development teams, Therapeutic Area Program Phase, Early Phase / Clinical Pharmacology, and Translational Medicine teams in new product development activities over the entire spectrum of drug development and clinical trial phases.
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3 years' experience in the pharmaceutical industry in drug development, clinical research experience, and/or marketing, market research, consumer engagement or consumer journey expertise.
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Seven years of experience in clinical research/drug development, including the design and implementation of large global clinical trials. In addition to his/her management and focused administrative responsibilities, the Associate Vice President – Medical Development drives strategic planning and, with operations teams and management, oversees the clinical research and overall medical support activities of the group.
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Excellent knowledge of drug development, clinical research operations and regulatory requirements including ICH-GCP, HCC and applicable regulations is required. Expertise or experience working in novel clinical research methods, particularly in digital and decentralized clinical trials is required.
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The Clinical Design Physician must have deep understanding of the biopharmaceutical industry, drug development, Diabetes-associated comorbidities, clinical research, and clinical study design.
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We are a market leader in automated bio sample management solutions and genomic services across areas such as drug development, clinical and advanced cell therapies for the industry's top pharmaceutical, biotech, academic and healthcare institutions globally.
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Our global teams of analysts, journalists and consultants keep their fingers on the pulse of the pharmaceutical, biomedical and medtech industries, covering it all with expert insights: key diseases, clinical trials, drug R&D and approvals, market forecasts and more.
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Five or more years of global regulatory CMC experience, or equivalent experience supporting CMC functions contributing to clinical trial phases of development in various regions, including US, EU, and Asia. Or 5 years’ experience in large molecule/biologics research and development or formulation.
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Oversight of clinical planning, budgeting, and execution Responsible for affiliate evaluation and input into clinical planning and contribution to clinical trials and communicates research needs to global Development team, Health Outcomes and Pricing, Reimbursement & Access (PRA) teams to ensure registration and post-registration clinical programs meet the needs of local/regional customers.
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