Regulatory Affairs Specialist-CC - Philadelphia

The Abramson Cancer Center (ACC) of the University of Pennsylvania seeks a Regulatory Affairs Specialist-CC to coordinate Phase I-V clinical trials. · Prepare and process all regulatory documentation through IRB, CTSRMC, FDA. · Organize and maintain regulatory affairs documentati ...

The Abramson Cancer Center (ACC) of the University of Pennsylvania seeks a full-time Regulatory Affairs Specialist-CC to participate in the coordination of Phase I-V clinical trials. · The successful candidate will prepare and process all regulatory documentation through the IRB, ...

The Abramson Cancer Center at the University of Pennsylvania seeks a full-time Regulatory Affairs Specialist-CC to participate in coordinating Phase I-V clinical trials. · ...

+The Abramson Cancer Center (ACC) of the University of Pennsylvania seeks a full-time Senior Regulatory Affairs Start-Up Specialist. · +Independently prepare and process regulatory aspects of clinical trial initiation. · +, A competitive benefits package including excellent healt ...

The Regulatory Affairs Specialist is responsible for preparing, reviewing, and maintaining regulatory submissions and documentation required for US FDA approvals of high-risk medical devices. · ...

Job summary: Regulatory Affairs Specialist to join one of our growing Medical Device clients in Audubon, PA. · ...

This is a hybrid position requiring the team member to be onsite a minimum of 3 days per week. The Medical Affairs Specialist at West is a global function dedicated to supporting the company's clinical activities and aligning with strategic goals to maintain high standards for pa ...

+The Medical Affairs Specialist at West is a global function dedicated to supporting the company's clinical activities and aligning with strategic goals to maintain high standards for patient safety and support regulatory obligations. · ...

The Medical Affairs Specialist at West is a global function dedicated to supporting the company's clinical activities and aligning with strategic goals to maintain high standards for patient safety and support regulatory obligations. · PharmD degree required · Minimum of 3 years ...

Supports necessary regulatory activities required for product market entry. · ...

IntePros is currently looking for a Sr. Regulatory Affairs Specialist to join one of our growing Medical Device clients in Audubon, PA. · ...

We have an incredible opportunity for a Scientific Affairs Specialist I to join ICON's Scientific Affairs team.The role assists in scientific knowledge and expertise across assay technologies, laboratory services, and clinical trial applications. · ...

IntePros is currently looking for a Lead Regulatory Affairs Specialist to join one of our growing medical device/manufacturing clients in Audubon, PA. · ...

We have an incredible opportunity for a Scientific Affairs Specialist II to join ICON's Scientific Affairs team.This role assists in scientific knowledge and expertise across assay technologies, laboratory services, and clinical trial applications. · ...

We have an incredible opportunity for a Scientific Affairs Specialist I to join ICON's Scientific Affairs team. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developme ...

We have an incredible opportunity for a Scientific Affairs Specialist I to join ICON's Scientific Affairs team. The role assists in scientific knowledge and expertise across assay technologies, laboratory services, and clinical trial applications. · ...

We have an incredible opportunity for a Scientific Affairs Specialist I to join ICON's Scientific Affairs team. · ...

The External Affairs Support Specialist will support the State Government Affairs, Regional Public Affairs and Outreach functions within Corporate Citizenship. · The position will be responsible for negotiating and maintaining contracts with external consultants, handling the pro ...

The Sr. Specialist, Regulatory Affairs, Medical is responsible for influencing department regulatory processes and procedures, · Develop and implement medical device regulatory strategies for West's administration and safety system product portfolio with an emphasis on gaining re ...

We have an incredible opportunity for a Scientific Affairs Specialist II to join ICON's Scientific Affairs team. · Maintain and configure testing and assay summary information in the Test Master application of the ICOLIMS system · Configure test codes within the STARLIMS system · ...