Senior Manager, Drug Safety Operations

Bracco Diagnostics Inc. is a subsidiary of Bracco Imaging which is part of the overall Bracco Group. The Company specializes in the clinical development, marketing and sales of diagnostic contrast imaging agents. Bracco Diagnostics Inc. primarily markets its products to hospitals throughout the United States. Bracco Diagnostics Inc. is committed to the discovery, development, manufacturing and marketing of imaging agents and solutions aimed at providing a better use and management in terms of diagnostic efficacy, patient safety and cost effectiveness. Job Purpose The Senior Manager, Safety Operations – DSPUS is responsible for overseeing pharmacovigilance operational and compliance activities for the Americas and ROW regions, ensuring full and continuous compliance with global and local regulatory requirements with a primary focus on BlueEarthDiagnosticInc. The role provides operational governance, compliance oversight, and strategic coordination of safety operations, acting as a key interface between DSPUS, global CDSP functions, Corporate PV Quality Systems, affiliates, distributors, and third‑party partners. Main Responsibilities, Activities, Duties, and Tasks Provide senior oversight of pharmacovigilance operational activities within DSPUS, including case management, submissions, reconciliations, and safety data management. Ensure timely and compliant processing and reporting of ICSR submissions to health authorities (e.g., FDA, Health Canada, NMPA, etc.) and business partners. Oversee operational performance and workload distribution within the DSPUS organization and across vendors or partners, as applicable. Ensure continuous compliance of DSPUS safety activities with global and local regulatory requirements, internal SOPs, working instructions, and PV agreements. Manage common mailbox oversight (BED and DSPUS) and reconciliations, including PADER and PSUR/PBRER appendix preparation when applicable. Prepare contractual and PVA documentation. Actively support PV audits and regulatory inspections for BED, including inspection readiness activities, participation in audits/inspections, and management of inspection outcomes and follow‑up actions. Contribute to the continuous improvement of the Pharmacovigilance Quality System through trend analysis, metrics, and feedback to corporate functions. Serve as a key operational and compliance interface with Corporate PV Quality Systems & Risk Management, Global Risk Assessment (GRA), Safety Systems/IT, Regulatory Affairs, Medical Affairs, Clinical, and other cross‑functional stakeholders. Coordinate PV‑related activities with distributors in the Americas and ROW regions. Act as a DSPUS escalation point for complex operational and compliance issues. Supervisory Responsibilities Not Applicable. Education University degree in Pharmacy, Pharmaceutical Chemistry and Technology, or a related scientific discipline. Professional Experience, Knowledge & Technical Skills At least 5 years of experience in pharmacovigilance, preferably in a multinational and matrixed organization. Knowledge of pharmacovigilance regulations (GVP, FDA, EMA, ICH). Ability to organize, prioritize, and work effectively in a constantly changing environment. Excellent oral and written communication skills in English. Ability to influence and build relationships/earn credibility quickly across broad global constituencies with competing priorities. Strong organizational skills; team player. Experience and skills with cross‑functional and highly matrixed organizations. Core Relationships Effective interaction with other Drug Safety staff and personnel from other departments within Medical and Regulatory Affairs (Medical Affairs & Scientific Information, Clinical Research, Biometrics and Medical Writing, Medical Planning and Management, Regulatory) to assure regulatory compliance and support to drug safety related activities; interaction with Information Technology Services, Corporate Quality Management and BDI Quality Operations, appropriate Legal Department (when applicable); operational contact with distributors, partners, and affiliates for PV‑related activities. Work Environment The employee must be able to communicate via telephone, written correspondence, or spoken word in order to perform the essential duties of the position. Bracco Diagnostics Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, or any other protected status. Improve people’s lives by shaping the future of prevention and precision imaging. This is our purpose. Our work impacts millions of people all over the world. Not least the more than 4,000 Bracco colleagues who work to improve lives every single day. That is quite a responsibility and something we proudly embrace. We are the Bracco Group! #J-18808-Ljbffr Bracco Diagnostics Inc.