Senior Regulatory Affairs Specialist Jobs in Chicago, IL

Join a dynamic team to provide comprehensive regulatory support across clinical, submission, and post-approval phases for pharmaceutical products, ensuring compliance with global regulations while man...

Champion regulatory compliance by supporting quality processes and product lifecycle management in the medical device sector, ensuring adherence to standards during design, development, and commercial...

Reimagine Regulatory Affairs by leading complex outsourcing programs and driving client success. Utilize deep expertise in strategy and operations to manage projects, mentor teams, and deliver tailore...

Join a team that's committed to ensuring regulatory compliance for diagnostic products. As a Senior Regulatory Affairs Specialist, you will assess regulatory impacts, prepare submissions, and collabor...

Champion regulatory excellence by guiding cross-functional teams in FDA advertising compliance while mitigating risks and enhancing strategic communications to support business goals...

Lead the charge in regulatory strategy for clinical studies, providing expert guidance on complex global compliance. Drive communication with health authorities and ensure timely documentation while c...

Take ownership of U.S. regulatory submissions, ensuring accuracy and compliance with FDA requirements. Collaborate cross-functionally to coordinate IND, NDA, and BLA filings, executing processes withi...

Champion regulatory excellence by leading global strategies for product approvals, collaborating with cross-functional teams and external experts to ensure compliance and drive successful commercializ...

Join a dynamic team and lead regulatory strategies for in vitro diagnostics, ensuring compliance and successful submissions while collaborating cross-functionally. Manage project timelines and mentor...

Join a team that's shaping the future of active implantable medical devices by supporting clinical evaluations and regulatory submissions. Collaborate across disciplines to ensure compliance with EU a...

Join a team that's committed to executing quality assurance for drug substance manufacturing, ensuring compliance with cGMP standards while supporting cross-functional collaboration and continuous imp...

Advance your career by managing Veeva RIM and Promo Mats systems, collaborating on regulatory processes, and enhancing data integrity within global regulatory affairs. Drive initiatives that ensure co...

Accelerate your impact by winning high-value, complex opportunities through innovative workflow design and technical expertise, while shaping market direction and influencing strategic commercial deci...

Optimize regulatory compliance initiatives within healthcare departments, ensuring adherence to CMS and DOH regulations. Collaborate effectively with multiple teams to assess risks, develop action pla...

Join our team to lead auditing and QA activities, ensuring compliance with regulations in clinical study sites. Collaborate with auditors and mentor staff while maintaining high standards for internal...

Transform compliance processes by leading a high-performing team of 20-25 in medical device regulation. Drive efficiency, quality, and adherence to standards while ensuring successful MDR submissions...

Transform regional regulatory engagement by leading strategy, fostering relationships, and advocating for efficient electric transmission policies. Collaborate across departments to align regulatory g...

Drive regulatory strategy to ensure successful US drug and biological product development and approval. Collaborate with cross-functional teams to achieve compliance, maintain communication, and suppo...

Transform regulatory practices by leading licensing projects and enhancing compliance frameworks. Collaborate with cross-functional teams to effectively manage commercial nuclear challenges and secure...

Explore a rewarding Senior Clinical Research Associate role managing relationships and ensuring quality in clinical trials across various therapeutic areas, with a strong focus on patient safety and c...

Lead strategic execution for global Risk Management initiatives, managing projects and delivering high-quality documentation across cross-functional teams while ensuring compliance with regulatory sta...

Unlock potential by driving post-market surveillance initiatives, ensuring regulatory compliance, and enhancing product safety through data analysis and collaboration with stakeholders across diverse...

Lead the charge in ensuring data quality, integrity, and governance, impacting regulatory compliance and patient safety across essential business operations. Drive high-impact analytics and continuous...

Accelerate progress at the forefront of global regulatory affairs by leading strategies for IND/CTA approvals, ensuring product launches, and executing post-marketing initiatives in the oncology secto...

Innovate global regulatory strategies to secure market approvals. Lead cross-functional teams, driving compliance and aligning with corporate goals in the pharmaceutical sector. Manage product life cy...