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 ...

University Overview · The University of Pennsylvania, the largest private employer in Philadelphia, is a world-renowned leader in education, research, and innovation. This historic, Ivy League school consistently ranks among the top 10 universities in the annual U.S. News & World ...

University Overview · The University of Pennsylvania, the largest private employer in Philadelphia, is a world-renowned leader in education, research, and innovation. This historic, Ivy League school consistently ranks among the top 10 universities in the annual U.S. News & World ...

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. · ...

+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. · ...

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. · PharmD degree required · Minimum of 3 years ...

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. 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. · ...

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. 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 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 · ...

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 ...

Job Summary · Under close supervision, assists key stakeholders with regulatory inquiries, safety data sheet authoring, data management, and global product stewardship support. · Job Description · Assist the Product Stewardship team with a variety of administrative and data manag ...

The Principal Specialist is responsible for influencing department regulatory processes and procedures, developing strategies for worldwide regulatory approval, preparing global submissions including Premarket Notifications, Global Registrations, Technical Documentation for CE Ma ...

· Company Description · A Few Words About Us · Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. ...

The Principal Specialist, Regulatory Affairs (Medical Devices) is responsible for influencing department regulatory processes and procedures, · developing strategies for worldwide regulatory approval, · preparing global submissions including Premarket Notifications, · Global Regi ...

This is a hybrid position requiring the team member to be onsite a minimum of 3 days per week. · The Principal Specialist, Regulatory Affairs (Medical Devices) is responsible for influencing department regulatory processes and procedures, developing strategies for worldwide regul ...

The Sr. Specialist, Regulatory Affairs is responsible for influencing department regulatory processes and procedures developing strategies authoring reviewing and supporting global registrations including Premarket Notifications China NMPA Registrations Technical Documentation fo ...