Senior Global Clinical Safety Leader

pThe strongGlobal Clinical Safety Physician /strong is a the senior clinical safety expert and reports directly to the Global Patient Safety Head. The Global Patient Safety Manager is responsible for developing, managing, executing, and overseeing all aspects of the safety programmes for one (or more) pipeline asset(s) throughout the product(s') life cycle. GPSM plays a key role in coordinating technical functions within GPS to facilitate these responsibilities. The individual is accountable for collaborative contributions and partnerships with the integrated development or product team to deliver on these safety commitments, while also demonstrating GPS expertise and leadership. /ppstrongKey Responsibilities Include: /strong /pulliProvide GPS Medical leadership and ensure proactive pharmacovigilance for assigned product(s) /liliDemonstrate advanced knowledge of safety concepts, per ICH, US, and international regulation/guidelines and GxP. /liliSynthesize complex data into actionable insights and translate technical issues into strategic discussions. /liliBuild strong relationships with key stakeholders, representing and championing the role of safety in the organization. /liliRepresent GPS Medical in inspections and audit activities. /liliFoster and support a collaborative working environment focused on inclusion, innovation, acceleration, and delivery. /liliProvide training, coaching, and mentor. /liliExperience and knowledge sharing to further advance the goals of the GPS group and wider enterprise. /liliMaintain compliance with corporate policies and relevant training curriculum. /li /ulpstrongEducation: /strong /pulliDegree in Medicine; PhD (or other complementary degree) in scientific discipline is preferred. /li /ulpstrongExperience: /strong /pulliMinimum 5+ years’ experience in the pharmaceutical industry or clinical care setting. /liliExperience in neuroscience or rare disease area is a plus. /liliKnowledge of drug development process /liliDirect experience with global regulatory filing and interacting with major regulatory agencies e.g., FDA advisory Committees, Scientific Advice, etc. /liliExpertise in pharmacovigilance with deep knowledge of regulatory requirements and guidelines pertaining to drug safety. /liliThorough knowledge and understanding of safety, including clinical safety, deliverables, standards, and processes at a global level; including pre and post launch experience. /liliProven record of successful clinical safety delivery with demonstrated examples of strategic influence to portfolio/clinical studies/programs. /liliDemonstrated success in implementing projects and/or innovating. /li /ulpstrongSkills, Knowledge Abilities /strong /pulliStrong analytical skills with the ability to critically interpret and apply scientific and clinical data for risk assessment and management. /liliProficient understanding of epidemiology and statistics, with the ability to apply data-driven decision-making. /liliFluent in English with highly effective written and verbal communication skills /liliExcellent interpersonal, organizational and negotiation skills /liliReceptive, engaging, and impactful contributor /liliAbility to thrive in a matrixed environment, effectively collaborating across cross-functional teams including Regulatory, Clinical Development, Medical Affairs, Commercial, and Quality. /liliStrong problem-solving and critical thinking abilities, with a demonstrated ability to manage complex issues and competing priorities. /liliAbility to work on multiple projects and function effectively in a fast-paced matrixed environment. /liliCommitment to business ethics and compliance, ensuring alignment with corporate values, industry regulations, and best practices. /li /ulpstrongAngelini Pharma is an equal Opportunity Employe /strong /ppWe believe that diversity is a huge value that contributes to individual and company success. We are committed to create a diverse and inclusive environment. /p #J-18808-Ljbffr