Sr. Director, Clinical and Regulatory Writing - Philadelphia, PA

This role can be remote, hybrid or based in our Philadelphia PA headquarters The Senior Director Clinical and Regulatory Writing will serve as a strategic leader within the Clinical Medical and Regulatory organization overseeing the development and delivery of high-quality regula ...

+Job summary · The Associate Director, Medical Writing, is responsible for the efficient preparation of high-quality, strategically aligned medical writing deliverables within one or more program.S/he will work directly with cross functional teams to author regulatory documents ( ...

A growing medical device organization seeks a Manager, Regulatory Affairs to lead U.S. regulatory submissions for Class II and Class III products. · Bachelor's degree in engineering, life sciences, or related technical field (Master's preferred) · 8+ years in the medical device i ...

We are seeking a highly motivated Associate Attorney to join our aviation law practice. · The ideal candidate will have a strong interest in aviation and regulatory law. · Excellent research and writing skills. · The ability to manage matters independently while working collabora ...

We are seeking a highly motivated and experienced Regulatory Affairs Director to support the development and implementation of global regulatory strategy for our next-generation precision oncology company focused on the development of Plixorafenib. · ...

Magnolia is pioneering a new era in environmental stewardship by leveraging compliance-based markets to drive large-scale conservation efforts. · ...

Magnolia is an environmental conservation company developing mitigation projects across the United States. As an Environmental Market Analyst intern at Magnolia you will have the opportunity to join one of the company's core teams working alongside people at vanguard of complianc ...

We're powering a cleaner, brighter future. Exelon is leading the energy transformation, and we're calling all problem solvers, innovators, community builders and change makers. We are a Fortune 200 company.Are you in? · A senior lawyer who is a highly qualified attorney handling ...

We are hiring for a Project Geologist to contribute to our EHS projects on a full-time basis while based at our office in Philadelphia. · Task and project management · Eeffectively organizing reports, proposals, and other documents · Oversight of junior staff for specific project ...

The Licensing Specialist supporting Combined Insurance will support the development and execution of key producer code maintenance and oversee the licensing process related to producer management systems as part of the Producer Services team. · ...

We are searching for a highly self-motivated postdoctoral fellow to join the Gan lab within the Aging + Cardiovascular Discovery Center. · The candidate will be expected to possess superior communication skills and present their research findings at national and international mee ...

We unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana.Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understan ...

The design quality engineer collaborates with design and manufacturing teams to ensure full compliance with design control standards such as 21 CFR 820 and ISO 13485.Responsibilities include developing, reviewing, and approving Design Inputs/Outputs, Design History File (DHF) doc ...

The University of Pennsylvania seeks an Associate Director for Regulatory Affairs to oversee clinical research regulatory operations. The successful candidate will have expertise in GCP regulations and experience with IND/IDE/Expanded Access Applications. · Oversight of regulator ...

The primary responsibilities for this position are to attend and participate in PJM stakeholder meetings and, within days of each meeting, write succinct reports, · with analysis where appropriate, on important presentations, announcements, discussions, · and other developments f ...

The primary duty of the Director of Compliance and Survey Management is to prepare for and support regulatory compliance and surveys as assigned. · This role is a residence support role. · ...

The primary duty of the Director of Compliance and Survey Management is to prepare for and support regulatory compliance and surveys as assigned. · This role is a residence support role that will spend the majority of time on-site at residences. ...

The American Association for Cancer Research AACR is dedicated to advances in all areas of high-quality innovative cancer research. The Scientific Program Administrator will manage key aspects related to planning and execution of several scientific conferences and workshops per y ...

The Director of Compliance and Survey Management is responsible for preparing for and supporting regulatory compliance and surveys. This role involves implementing training schedules, conducting audits, providing support to residence leaders, and ensuring quality monitoring proce ...

Cytokinetics seeks an Associate Director for Clinical Trial Transparency to support all aspects of CTT at the company. · ...