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Working within pharma in both biologic development and cell and gene therapy and reporting directly to the Senior Director of Global Compliance. 5+ years QA GCP/GLP experience (biopharma/cell & gene therapy a plus.
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We are currently seeking an experienced and motivated individual to fill the role of Associate Director/Director Clinical Operations with our client, a small start-up immuno-oncology biotech company located in Montgomery County, Maryland.
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As we chart new territories in therapeutic breakthroughs, we're actively seeking an exceptional Associate Director of Clinical Operations to be a driving force in our revolutionary projects.
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5+ years QA experience (biopharma/cell & gene therapy a plus) Experience leading/participating in regulatory GCP/GLP audits. Lead audits, ensuring GCP/GLP compliance. Solid regulatory audit experience (FDA a plus.
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Company Summary: A global immunology focused pharmaceutical group with an impressive track record is seeking an Associate Director of Clinical Operations for a hybrid role located in Palo Alto, CA. Their commercial supply of pharmaceutical products generated $83m in revenue in FY2023 (a 24% uptick from the year prior.
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Join a dynamic immunology biotech as the Associate Director of Clinical Operations. Join a dynamic immunology biotech as the Associate Director of Clinical Operations. Minimum of 7-10 years of experience in clinical operations within the biopharmaceutical or biotechnology industry, with specific experience in immunology preferred.
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Lead the planning and execution of clinical trials for immunology therapeutics, ensuring adherence to protocols, timelines, and budgetary constraints. In-depth knowledge of clinical trial regulations, guidelines, and industry standards (e.g., ICH-GCP.
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They are looking to add a Global Regulatory Affairs Labeling Associate Director to their team on a hybrid basis to their site in Wilmington, DE! Associate Director, Global Regulatory Affairs Labeling.
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The Global Regulatory Affairs Labeling Associate Director should have the following qualifications:Bachelor's degree and 4+ years of direct regulatory labeling experience in the pharmaceutical industry.
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I am partnered with a growing biotech company located in San Francisco who is looking for an Associate Director of DMPK to join their team! I am partnered with a growing biotech company located in San Francisco who is looking for an Associate Director of DMPK to join their team.
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Participate in the drafting, review, and finalization of clinical study protocols and study analysis plans (SAP)
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Hiring an Associate Director Biostatistics. Hiring an Associate Director Biostatistics. PhD in Statistics or Biostatistics. Provide in-depth knowledge of clinical trials methodology, regulatory requirements, and statistics.
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Associate Director Quality Control. Relocation assistance provided for non-local candidates. Monitor and trend data while assembling reports on product release test monitoring of the company cGMP facility.
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QA Leader to support the quality management systems and processes for a CRO based in Burlington. Champion a strong quality culture within the team. Shape and expand our US quality management systems.
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Drive continuous improvement in quality processes. Passion for quality and cultural change leadership. Excellent communication, teamwork, and leadership skills. Oversee systems, suppliers, and employee training.
ExpandApply NowActive JobUpdated 13 days ago
Title: associate director Company: Epm Scientific
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