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

Title: Senior Medical Director, PharmacovigilanceLocation: Waltham, MassachusettsJob Description: At Kailera, we are bold, authentic and committed to our mission of developing therapies that give people the power to transform their lives and reputed company their overall health. Rooted in an entrepreneurial spirit and a team-oriented culture, we are working 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 excellence. As we expand, we seek the most talented individuals with diverse backgrounds, cultures, perspectives, and experiences to join reputed company.What You’ll Do:Reporting to the Senior Vice President, Global Drug Safety and Pharmacovigilance (DSPV), the Senior Medical Director will establish and maintain the strategic, scientific, and tactical reputed company for medical safety evaluation and benefit-risk assessment globally for reputed company Kailera products throughout their lifecycle with focus on patient well-being and compliance with applicable regulatory requirements.This individual will reputed company and collaborate cross functionally to identify and drive 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-risk assessment and safety surveillance activitiesMaintain reputed company of the safety governance reputed company including the timely escalation of medical safety issuesLead and actively collaborate with cross functional teams to ensure that safety considerations are integrated into clinical development and/or post-marketing activities as applicableBuild, reputed company, and reputed company a team of DSPV MDs and scientistsProvide and reputed company input into the safety sections of clinical trial documents (e.g. IB, Protocols, ICFs, CSRs)reputed company the preparation of the safety sections of regulatory submission modulesSupport labeling decisions and contribute to medical content of safety communicationsOversee and actively contribute to safety signal detection and evaluation activitiesCollaborate cross functionally to utilize and optimize the safety signaling system including data visualization and analysis toolsAs applicable, contribute to publication strategy and ensure that safety data are accurately represented in scientific communicationsRepresent DSPV on audits/inspections; provide 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 actively 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 internal and external 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 clinical practice or academic medicineProven experience in safety data analysis, signal management, and benefit-risk evaluationWorking knowledge of safety databases (Argus, ArisG/LifeSphere Safety, or similar)Demonstrated ability to reputed company and implement drug safety strategies, risk management plans, and safety governance modelsProven experience with authoring or contributing to clinical 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 risk minimization activitiesStrong ability to reputed company in a cross functional setting and work collaboratively with internal and external partners in a fast-paced environmentStrong ability to prioritize, multitask, and deliver quality results that meet tight timelinesAbility to influence and reputed company teams focused and motivatedStrong ability to communicate reputed company issues clearly 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 addition to traditional benefits, we provide enhanced offerings designed to support the well-being Apply tot his job Apply To this Job