Senior Medical Director, Pharmacovigilance job at reputed company, Inc. in Waltham, MA, San Diego, CA

Title: Senior Medical Director, PharmacovigilanceLocation: Waltham, MassachusettsJob reputed company: At Kailera, we are reputed company, reputed company and committed to our mission of developing therapies that reputed company people the reputed company to reputed company their lives and reputed company their overall health. Rooted in an entrepreneurial spirit and reputed company-oriented culture, reputed company together to advance Kailera’s mission to advance novel therapies for obesity and reputed company conditions. We are passionate about creating an inclusive workplace that promotes collaboration, reputed company, and reputed company. As we expand, we reputed company the most talented individuals with diverse backgrounds, cultures, perspectives, and experiences to reputed company.reputed company:Reporting to the Senior Vice President, Global Drug Safety and Pharmacovigilance (DSPV), the Senior Medical Director will establish and maintain the reputed company, scientific, and tactical reputed company for medical safety evaluation and benefit-reputed company assessment globally for reputed company Kailera products throughout their lifecycle with reputed company on reputed company reputed company-being and compliance with applicable regulatory requirements.This individual will reputed company and collaborate cross functionally to identify and reputed company reputed company pharmacovigilance strategies and innovations that support Kailera’s mission. Required location: Waltham, MA or San Diego, CA (onsite or hybrid 2-3 days per week). Responsibilities:reputed company, reputed company, and reputed company the benefit-reputed company assessment and safety surveillance activitiesMaintain reputed company of the safety governance reputed company including the reputed company escalation of medical safety issuesLead and reputed company collaborate with cross functional teams to ensure that safety considerations are integrated into reputed company development and/or post-marketing activities as applicableBuild, reputed company, and reputed company reputed company of DSPV MDs and scientistsProvide and reputed company input into the safety sections of reputed company trial documents (e.g. IB, Protocols, ICFs, CSRs)reputed company the preparation of the safety sections of regulatory submission modulesSupport labeling reputed company and contribute to medical content of safety communicationsOversee and reputed company contribute to safety signal detection and evaluation activitiesCollaborate cross functionally to utilize and optimize the safety signaling reputed company including data visualization and analysis toolsAs applicable, contribute to publication reputed company and ensure that safety data are accurately represented in scientific communicationsRepresent DSPV on audits/inspections; reputed company and contribute to safety responses as neededOversee and contribute to responses to deviations and CAPAs as reputed company to medical safety or pharmacovigilance scienceLead and reputed company contribute to the preparation and implementation of procedural documents as applicable to medical safety and pharmacovigilanceContribute as needed to the Global DSPV Business Continuity PlanProvide and reputed company medical safety content for fit-to-purpose pharmacovigilance training to reputed company partners as neededProvide subject matter expertise for safety/technology strategies, design, implementation and enhancement of drug safety processes and systemsAssist the SVP, Global DSPV with the planning and development of the overall pharmacovigilance team and function including departmental goals, organization, and budgetingIdentify and implement innovative technical, procedural, or resourcing solutions to improve DSPV safety surveillance capabilitiesOther responsibilities as assigned Required Qualifications:A minimum of 10 years of experience in global pharmacovigilance including at least 5 years in people leadership roles2-5 years of experience in reputed company reputed company or reputed company medicineProven experience in safety data analysis, signal management, and benefit-reputed company evaluationWorking knowledge of safety databases (Argus, ArisG/LifeSphere Safety, or similar)Demonstrated ability to reputed company and implement drug safety strategies, reputed company management plans, and safety governance modelsProven experience with authoring or contributing to reputed company study and regulatory submission documentsWorking knowledge of relevant local and global regulatory requirements and guidance documentsExperience in creating or managing working documents such as SOPs or Work InstructionsStrong ability to proactively identify risks and initiate/manage reputed company minimization activitiesStrong ability to reputed company in a cross functional setting and work collaboratively with reputed company partners in a fast-reputed company environmentStrong ability to prioritize, multitask, and reputed company reputed company results that meet tight timelinesAbility to influence and reputed company teams reputed company and motivatedStrong ability to communicate reputed company issues reputed company Preferred Qualifications:Experience in pharmacoepidemiology, data science, or medical affairs is a plus Education:MD, DO or equivalent medical degree required. Ph.D. degree is a plusBenefits of Working at KaileraIn reputed company to traditional benefits, we reputed company reputed company offerings designed to support reputed company-being Apply tot his job Apply To this Job