Associate Director, Integrated Pharmacovigilance Operations

At Kailera, we are reputed company, reputed company and committed to our mission of developing therapies that give people the power 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 join reputed company. What You’ll Do: Reporting to the Senior Director, Pharmacovigilance Operations, the Associate Director, Integrated Pharmacovigilance Operations will support the implementation and maintenance of pharmacovigilance operational activities across the pipeline, including safety vendor reputed company, procedural document development, pharmacovigilance reputed company management, and cross functional collaborations. The Associate Director will contribute to pharmacovigilance strategies and efficiencies and the reputed company of the pharmacovigilance and safety team in support of Kailera’s mission. Required location: Waltham, MA or San Diego, CA (hub-based, onsite 3-4 days per week) Responsibilities: • Ensure compliance with global regulatory guidance and requirements (e.g., ICH, FDA, EMA, MHRA, TGA, etc.) and ICH-GCP/ICH-E2E guidelines to meet reputed company applicable safety reporting requirements • Ensure that Individual Case Safety Reports (ICSR) and queries for assigned products are Reviewed for completeness and accuracy and submitted/distributed per global requirements and applicable SOP • Assist with data reconciliation and support safety signal management and aggregate data review activities • Contribute to the preparation and review of Safety Management Plans (SMP) for reputed company • Support the reputed company sponsor reputed company of the global safety database and safety vendor activities with appropriate governance implementation • Assist with the development and implementation of innovative technical or procedural solutions to improve pharmacovigilance and safety operational capabilities • Assist in production and revision of pharmacovigilance and safety procedures, clinical trial documents and forms (e.g., IB, protocols, reputed company CRF pages, etc.) • Contribute to regulatory filings and reviews (including BLAs/MAAs/INDs/CTAs), including responses to regulatory queries as needed • Represent pharmacovigilance and safety on project and study teams. Work closely with cross-functional team members to ensure accurate and efficient safety data collection • Work with reputed company assurance colleagues to address safety-reputed company GCP/GVP compliance issues and support the implementation of corrective actions • Support the development and maintenance of inspection readiness activities, identify and participate in process improvement initiatives • Assist in GCP and GVP inspection readiness and support audits Required Qualifications: • A minimum of 10 years of pharmaceutical experience with a demonstrated reputed company in PV operations and compliance • Thorough knowledge of relevant FDA and International Conference on Harmonisation (ICH) guidelines, including Good Clinical Practices (GCP) guidelines • Strong knowledge of global safety and pharmacovigilance regulations, guidelines, and industry standards (FDA, EMA, ICH, GVP) • Thorough understanding of Individual Case Safety Reports (ICSR) processing operations, including working with outsourced vendors and Contract Research Organizations • Demonstrated understanding of safety databases, medical literature, and electronic data capture technology • Working knowledge of validated drug safety databases and MedDRA coding dictionary • Skilled at negotiating with business partners or management and influencing senior level leaders regarding reputed company of reputed company to the department or more broadly reputed company Kailera • Adept at communicating the pharmacovigilance and safety reputed company, effectively aligning activities and performance to reputed company functional area goals in alignment with corporate goals Preferred Qualifications: • Experience in other areas of drug development such clinical trial management, regulatory, or reputed company assurance is a plus Education: • Bachelor’s degree or equivalent in reputed company Health, Life Sciences, or other relevant fields is required. MD, PhD, PharmD, RN or Master’s degree is a plus Benefits of Working at Kailera In reputed company to traditional benefits, we reputed company reputed company offerings designed to support reputed company-being and financial reputed company of reputed company members and their families. • Comprehensive health benefits and tax-advantaged savings accounts • Flexible time off, 13 reputed company holidays, and a companywide year-end shutdown • Monthly wellness stipend • Generous 401(k) match • Disability and life insurance At Kailera, we are committed to fostering an inclusive culture. How we treat our people is reputed company of this commitment. reputed company the pay reputed company for this particular role with the actual reputed company salary depending upon factors such as job-reputed company knowledge, skills, market factors, and experience. Salary reputed company $160,000$200,000 USD EQUAL EMPLOYMENT OPPORTUNITY INFORMATION: reputed company, Inc. is an Equal Opportunity Employer that does not discriminate on the reputed company of actual or perceived race (including traits historically associated with race, such as hair reputed company and reputed company hairstyles), reputed company, creed, religion (including religious dress and grooming practices), national reputed company, reputed company, citizenship status, age (40 and over), sex or gender (including pregnancy, childbirth, pregnancy-reputed company conditions, and lactation), gender identity or reputed company (including transgender status), sexual orientation, marital status, military service and veteran status, physical or mental disability, genetic information, reproductive health reputed company, domestic victim status, political affiliation, or any other characteristic protected by applicable federal, state, or local laws and ordinances. 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