- Boehringer Ingelheim (Ridgefield, CT)
- **Description** The Clinical Development and Medical Affairs Fellow is a post - doctoral pharmacist position that will obtain broad exposure to BI US Medical ... Scientific Communications, clinical operations, translational medicine and clinical pharmacology, and regulatory affairs . This position will require the Fellow… more
- Boehringer Ingelheim (Ridgefield, CT)
- …The Regulatory Affairs Fellow - Advertising and Promotion is a post - doctoral pharmacist position that will obtain broad exposure to BI US Medical ... Scientific Communications, clinical operations, translational medicine and clinical pharmacology, and regulatory affairs . This position will require the Fellow… more
- Boehringer Ingelheim (Ridgefield, CT)
- … strategy expertise/knowledge in one or more therapeutic areas. Interact effectively within Regulatory Affairs and across functions, as a US regulatory ... goals for assigned projects, with supervision. With supervision, the Product Group Regulatory Affairs Fellow will: + Regulatory Professionalism: + As a … more
- Boehringer Ingelheim (Ridgefield, CT)
- **Description** The Regulatory Affairs Labeling Operations Fellowship is designed to provide pharmacists with exposure to regulatory requirements for US ... the opportunity to complete rotations in areas within and beyond Regulatory Affairs . This position will require the Fellow to develop competencies necessary… more
- Boehringer Ingelheim (Ridgefield, CT)
- **Description** The Regulatory Affairs Labeling Content Fellowship is designed to provide pharmacists with exposure to regulatory requirements for US product ... the opportunity to complete rotations in areas within and beyond Regulatory Affairs . This position will require the Fellow to develop competencies necessary… more
- Boehringer Ingelheim (Ridgefield, CT)
- …Outlook, Word, PowerPoint, and Excel.* Foundational understanding of corporate structure, regulatory considerations and the drug development process in pharmacy with ... of required trial documents, contracts and necessary approvals. * All Regulatory Requirements are satisfied prior to trial/site initiation. * Where necessary,… more
- Danaher Corporation (New York, NY)
- …of medical safety and compliance strategies with other departments (quality, regulatory , R&D, and others) + Support pre/ post -market activities including ... the Medical Safety & Compliance team, ensuring that Medical & Scientific Affairs are strategically positioned to provide timely medical and clinical consultation and… more