I. JOB OVERVIEW Job Description Summary: The Director, Regulatory Oversight position reports to the Associate... programs. The Director, Regulatory Oversight works closely with Office of Research Integrity and Compliance leadership, the...
take place and timely submissions are made to OPDP. Work closely with the Director, Regulatory Ad Promo to formulate the... and recommend/implement policy and/or process changes as needed in partnership with Director, Regulatory Ad/Promo Maintain...
Director in the Nonclinical Regulatory Writing and Systems (NRWS) Department within Preclinical and Translational Sciences (PTS...: Associate Director, Nonclinical Regulatory Writing and Submission Support, Oncology and Marketed Products At Takeda...
Monica, CA and reports to the Executive Director, CMC Regulatory Affairs. Responsibilities Interpret global regulations...Position Summary The AD CMC Regulatory Affairs supports the development and successful performance of the CMC...
regulatory sciences Experience in applicable therapeutic area Knowledge of Global regulatory procedures and practices... are determined to make life better for people around the world. Purpose: The purpose of the Senior Director/Executive Director...
. Job Type: Full time Job Title: Associate Director of Regulatory Affairs Location: Onsite - San Diego Salary... Range: $150,000 - $170,000 Position Summary: The Associate Director of Regulatory Affairs will play a crucial role in leading and managing the...
through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences... drug and device programs. The Director, Regulatory Labeling and Development Strategist is responsible for: Providing...
Director of Regulatory Affairs, Lifecycle Department: Regulatory Employment Type: Permanent - Full Time Location...: US (Remote) Reporting To: VP of Regulatory and Clinical Description The Director, Lifecycle RA provides strategic...
*Gene therapy experience preverred* Responsibilities: Actively represent Regulatory CMC and provide regulatory... and drive regulatory CMC submissions, including assembling necessary cross functional teams and timelines relevant to assigned...
to be a part of our Global Regulatory Affairs (GRA) organization. In this role, you will be primarily responsible for the... development of US/Global regulatory strategies to advance Lupin’s portfolio of development pipeline candidate drugs...
to be a part of our Global Regulatory Affairs (GRA) organization. In this role, you will be primarily responsible for the... development of US/Global regulatory strategies to advance Lupin’s portfolio of development pipeline candidate drugs...
Description For assigned development projects and US marketed products, provide experienced US regulatory leadership... to the global and US cross-functional teams. Provide US strategic regulatory guidance to facilitate efficient and compliant...
and company culture, visit us at | Who You Are This experienced regulatory professional will have demonstrated the... ability to work independently or with limited direction and oversight. The individual will manage internal regulatory processes...
Key Responsibilities: Manages the day-to-day regulatory activities of assigned projects for compounds... under development and/or marketed. These activities include acting as the regulatory representative on core teams, developing...
development. The Medical Director, Clinical Science should be a subject matter expert in internal medicine, have expertise in... team, and those on the regulatory, quality, strategy, and business teams. Guide clinical vision for the next generation...
listed, the Dean of CNHSB may request that the Divisional Director of Natural Sciences assume other responsibilities...Summary The Director leads the division, oversees long-range planning, initiates and coordinates curriculum...
Director of Clinical Performance Improvement - Behavioral Sciences Campus Position Summary: The Director... activities for UTHealth Houston's Behavioral Sciences Campus. The Director will provide overall administrative direction...
, publication preparation, and safety monitoring. SUMMARY DESCRIPTION The Associate Director / Associate Medical Director... across all stages of program and study design and execution, data analysis and regulatory filings as delegated by the Clinical Science...
, publication preparation, and safety monitoring. SUMMARY DESCRIPTION The Associate Director / Associate Medical Director... across all stages of program and study design and execution, data analysis and regulatory filings as delegated by the Clinical Science...
Job Description Summary As Associate Director, R&D, Materials Sciences, you will play a critical role in shaping the... and become your best self. Become a maker of possible with us. As Associate Director, R&D, Materials Sciences, you will become the architect...