- AbbVie (North Chicago, IL)
- …strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations, and emerging issues. ... project-related education of investigators, study site personnel, and AbbVie study staff . + Has overall responsibility for leading clinical study teams, monitoring… more
- AbbVie (North Chicago, IL)
- …strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations, and emerging issues. ... of scientific content of protocols, Investigator Brochures, Clinical Study reports, regulatory submissions and responses, and other program documents. + Manages one… more
- AbbVie (Irvine, CA)
- …opinion leader interactions related to the disease area(s); partners with Medical Affairs , Commercial and other functions in these activities as required, consistent ... strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations and emerging issues.… more
- JBS USA (Greeley, CO)
- … regulatory , and food safety practices. In this role, you will manage and advise regulatory staff with any labeling or regulatory issues. You will also ... co-packers. Additionally, you'll direct Customer Service/Sales and advise Consumer Affairs on complaints or technical questions. Responsibilities: + Lead, supervise,… more
- Zimmer Biomet (Englewood, CO)
- …with a firm grasp on design for manufacturing + Assist junior Engineering staff with modeling and detailing methodology + Lead efforts of new product development ... design efforts to minimize patient risk and adhere to regulatory requirements + Lead in development of testing protocols...inspection plans + Aide in publication efforts with Clinical Affairs team. + Lead surgical demonstrations (live, cadaver, or… more
- AltaGas (Springfield, VA)
- …in other areas of the organization that the EE programs depend upon, such as Regulatory Affairs , Public Policy, and the Office of General Counsel (OGC). + ... a project management capacity by coordinating and managing various planning, design, and regulatory compliance activities for a broad array of EE programs that are… more
- Ascendis Pharma (Princeton, NJ)
- …+ Functions as a PV advisor to Ascendis Clinical Development Organizations, Medical Affairs , Commercial Organizations and PV staff as applicable. + Identify ... create Corrective Action and Preventative action (CAPA) as applicable. + Oversee regulatory and departmental compliance by ensuring timely processing of ICSRs in the… more
- AbbVie (Irvine, CA)
- … staff . + Responsible for understanding and addressing applicable regulatory requirements related to the clinical studies, clinician reported outcomes, patient ... author, edit and review key section of research protocols, reports and regulatory submissions. Responsibilities: + Based on strong medical and scientific experience,… more
- Fujifilm (Dover, DE)
- …**Job Description** **Responsibilities** + Manage and support the day-to-day legal affairs of assigned Medical Device businesses or operating divisions, under the ... Division General Counsel and senior business management on general legal and regulatory risks affecting the Medical Device businesses, including with respect to… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …care and clinical care standards driven by patient safety and regulatory requirements, clinical outcomes monitoring, and patient and family experience expectations. ... the successful recruitment, retention, and development of outstanding faculty and staff . + Define and communicate expectations for faculty members, provides the… more