collaboration with stakeholders, such as Clinical Operations, Regulatory Affairs, Quality, Manufacturing, and Pro No matter... and company culture, visit us at | Who You Are The Director/Sr. Director, Clinical Supply Chain Management will be responsible...
regulatory plans and play a key role in regulatory meetings in partnership with regulatory affairs. Identify opportunities...Job Title: Executive Medical Director, Clinical Development -Neuroscience Job Location: Home, KS 66438, USA...
Director, Oncology Clinical Sciences in our Cambridge office. At Takeda, we are transforming the pharmaceutical industry... their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation...
with other functional leaders in CMC, Regulatory Affairs, Clinical Operation and Quality Assurance in support of the study project teams... Operations, Clinical Operations, Regulatory Affairs, Quality Assurance, and external vendors to execute the strategies for the...
Develop and lead clinical supply chain strategies to support global clinical trials, aligning with clinical, regulatory..., Regulatory Affairs, Manufacturing, and other internal & external stakeholders. Partner with Clinical Operations to align...
Job Description: The Associate Director, Clinical Operations is responsible for aspects of clinical development... accountability to a wide range of audiences · Partners directly with or guides staff to partner with preclinical, regulatory...
, and control systems to reduce costs, streamline procedures, and ensure regulatory compliance of the global supply chain. Works... with colleagues in CMC, QA, commercial, clinical, and regulatory affairs to ensure appropriate selection and oversight of vendors...
&D, Regulatory affairs, Global Clinical Safety & Pharmacovigilance and may serve on the Safety Management team for key US products... and collaborate with the global TA leads representing both Pipeline and In-line products, International Medical Affairs, CRD, R...
, Regulatory, Clinical Development, Clinical Operations, Compliance, Pharmacovigilance, Biometrics, Global Communications... expertise, and collaborate with Commercial, Legal, and Regulatory for development and review of Labeling, advertising...
, Regulatory, Clinical Development, Clinical Operations, Compliance, Pharmacovigilance, Biometrics, Global Communications... expertise, and collaborate with Commercial, Legal, and Regulatory for development and review of Labeling, advertising...
for understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying... principles, knowledge of compliance and regulatory requirements, AbbVie’s customers, markets, business operations and emerging...
Regulatory Affairs, and Worldwide Commercialization Excellence (WCE) on execution of all label updates and launches. The role... as required for Global Regulatory, Packaging, and R&D. Develop and maintain Universal Patient Language Important Safety Information aligned...
Managers and Medical Director. Ensure the scientific information is consistent with product labeling. Assist...The Opportunity: Global pharmaceutical company seeks a Medical Information Specialist - Oncology in New Jersey...
Managers and Medical Director. Ensure the scientific information is consistent with product labeling. Assist...The Opportunity: Global pharmaceutical company seeks a Medical Information Specialist - Oncology in New Jersey...
. You will report directly to the Medical Safety Director as a member of the global medical safety team. You must be adept..., Quality Affairs & Regulatory Affairs, Research & Development, Legal, and Health Care Compliance. Job Duties Complaint...
. You will report directly to the Medical Safety Director as a member of the global medical safety team. You must be adept..., Quality Affairs & Regulatory Affairs, Research & Development, Legal, and Health Care Compliance. Job Duties Complaint...
Affairs (GMDA), Field Training, Market Research, Business Analytics, Regulatory Affairs, Public Affairs, and Corporate... Executive Director & Head Therapeutics Counsel and will be responsible for providing legal support to business partners...
expectations and influencing others Working with cross functional team including Clinical Operations, Regulatory Affairs and QA..., labeling and distribution of investigational medicinal product to support Vertex clinical studies. This person delivers...
offers GMP secondary packaging and clinical labeling services throughout our global network. Packaging can be configured... global labeling system with its multi-lingual label phrase library we can design single panel, booklet labels or our unique...