Role Description The Global Safety Physician serves as the safety expert accountable for the global safety strategy and overall safety profile for Jazz Pharmaceuticals product/s (investigational and marketed) throughout their lifecycle. This includes supporting major pre- and post-marketing safety deliverables including signal, benefit-risk evaluation and risk management activities for specific products. This individual must effectively interface cross-functionally at all levels in the organization as well as with external Regulatory Authorities. The ability to work in a dynamic, changing environment to meet corporate and patient needs is essential. Essential Functions - Lead the preparation and review of safety-related section(s) for product/s, including clinical, regulatory, and scientific documents. - Be a key member, as the safety representative, to a Global Regulatory Team and to a Core Development Team. - Interface with Risk Evaluation and Mitigation Strategy (REMS) team to optimize risk management of assigned products. - Support creation and maintenance of Company Core Safety Information (CCSI) and ensure implementation in all Reference Safety Information (RSI). - Support review of medical/scientific literature for signal detection activities and aggregate reporting. - Support signal detection activities to ensure signal identification, evaluation, validation, and documentation of safety assessments. - Participate in or Lead a Safety Management Team (SMT) for an assigned product. - Contribute to the preparation and review of pre- and post-marketing aggregate safety reports. - Contribute to preparation of Risk Management Plans (RMPs) for assigned products. - Provide guidance with adverse event (MedDRA) and drug (WHO Drug) coding for clinical and postmarketing safety data. - Demonstrate or gain knowledge of current and applicable global PV regulations and guidelines. - Provide safety expertise to due diligence activities, if needed. - Keep abreast of new PV/safety regulations and guidance from regulatory authorities. Qualifications - Minimum 2-5 years of Clinical Development, Medical Affairs or Drug Safety/Pharmacovigilance experience. - Excellent knowledge of drug development process. - High level of initiative and independence. - Excellent written and oral communication skills. - Resourcefulness and personal organization skills. - Demonstrated cross-functional teamwork. - Computer literacy with proficiency in external Regulatory Databases, Microsoft Excel, PowerPoint, and Word. - Some national/international travel may be required. Leadership Skills - Enterprise and Proactive Mindset. - Set & Achieve Goals. - Inspire & Mobilize Others. - Understanding of target product profile; clinical designs and/or global PV regulatory environment. - Exposure to working relationship with the FDA, EMA, and other regulatory authorities is preferred. - Working knowledge of safety databases and electronic data capture systems is a plus. - MedDRA trained and working knowledge of MedDRA and WHO Drug coding dictionaries is a plus. - Ability to manage multiple tasks with deadlines in a fast-paced environment. Required/Preferred Education and Licenses - MD required; medical licensure in at least one region preferred. - Clinical research and/or fellowship training in internal medicine, oncology, neurology, or other relevant specialty is a plus. Benefits - Medical, dental, and vision insurance. - 401k retirement savings plan. - Flexible paid vacation. - Discretionary annual cash bonus or incentive compensation. - Discretionary equity grants in accordance with Jazz’s Long Term Equity Incentive Plan.

Role Description Join the team transforming care for people with immune challenges, rare diseases, cancers, and neurological conditions. In Specialty Care, you’ll help deliver breakthrough treatments that bring hope to patients with some of the highest unmet needs. The Medical Science Liaison (MSL) is a field-facing role whose main objectives are to: - Be the trusted scientific partner to key external experts by conducting timely, appropriate and frequent scientific exchanges to enhance the understanding of the scientific and medical value of our products. - Execute on stakeholder engagement plans to gather data, develop and share medical insights that contribute to enhancement of Sanofi’s key medical messages, plans and future research. - Keep abreast of medical and scientific developments in the therapeutic field to help identify and critically assess research opportunities and to play a supportive role in the execution of evidence generation plans to enhance the value of our products in a real-world setting. - Recognize, record and share insights that deepen our understanding of the needs of patients, consumers, regulators, payers, and healthcare providers and proactively contribute towards identifying unmet needs. - Maintain effective and appropriate communication among internal stakeholders (Medical Affairs colleagues, Medical Information and Commercial Operations) while maintaining full compliance with relevant company, industry, legal and regulatory requirements. - Demonstrate operational understanding and risk management by ensuring excellence in execution of all governance processes. Qualifications - Advanced degree in a technical, scientific or medical field (MD, PhD, Pharm D) preferred, or other relevant Life Science degree (RN/MS) with Rhinology and/or Gastroenterology Specialty required. - Must reside in territory. - Valid driver’s license with a clean driving record and ability to pass a complete background check. - Driving a company car in a safe manner to daily meetings and appointments is required. Requirements - Minimum of 2 years of experience in pharmaceutical industry, Medical Science Liaison role, or relevant clinical practice. Additional years of experience are an asset. MSL experience strongly preferred. - Clear understanding of medical practice, clinical decision making, and healthcare systems related to patient care. - Ability to interpret key scientific data and translate this information to meet educational and research needs. - Demonstrated ability to address educational and research needs through delivery of cutting edge scientific/evidenced based data. - Exemplary communication and presentation skills. - Experience in working on multi-disciplinary teams and managing significant volume of projects. Benefits - Bring the miracles of science to life alongside a supportive, future-focused team. - Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally. - Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact. - Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave. - This position is eligible for a company car through the Company’s FLEET program.

Role Description Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam D'Angelo, Larry Summers, and Jack Dorsey. Position: B2B Buyer at U.S. Health Plans Type: Contract Compensation: $121/hour Location: Remote Duration: One-time engagement — 30 minutes Role Responsibilities - Provide accurate insights based on your experience with PBM selection, contracting, and management. - Share perspectives on vendor evaluation, pricing, and performance metrics. - Complete all survey questions thoroughly and submit responses on time. Qualifications - Employed full-time or part-time. - Currently working at a U.S. health plan or health insurer. - Involved in PBM selection, contracting, or pricing. - Experience with renewals and vendor evaluation. - Ongoing PBM relationship management. - Decision-maker or key influencer in PBM-related decisions. Requirements - Application Process (Takes 20–30 mins to complete) - Upload resume - AI interview based on your resume - Submit form Resources & Support - For details about the interview process and platform information, please check: Interview Process Details - For any help or support, reach out to: support@mercor.com - PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.

Role Description The Specialty Care Field Medical, Director is responsible for providing therapeutic area/product expertise for the designated therapeutic area across a broad range of external medical stakeholders (“EMS”) and initiatives in an assigned territory (typically comprised of one or more US states). - Plan and execute independent Medical strategies and engagements for appropriate assigned external medical stakeholders within a territory, compliantly coordinating with other Pfizer colleagues as needed to achieve Medical objectives. - Maintain required level of knowledge of relevant TA/disease states and Pfizer medicines, providing therapeutic area/product information to both internal and external stakeholders as needed. - Serve as a conduit and resource for Medical Information and external medical stakeholder insights, providing requested information to external medical stakeholders as allowed by Pfizer guidance and sharing external medical stakeholder viewpoints with Pfizer as appropriate. - Understand the priorities of Pfizer Medical Affairs in order to contribute to Medical educational content strategy development and execute aligned Field Medical tactics. - Maintain effective and appropriate scientific communication and collaboration among headquarters Medical colleagues, Medical Information, and other Pfizer Field Medical colleagues. - Demonstrate expertise in scientific communication across multiple channels, including, but not limited to, live and virtual presentations in small or large settings, written communication, and telephone or virtual conversations. - Optimize patient care improvement in Medical communications and deliverables, incorporating Health Literacy and cultural awareness principles to ensure that patients remain the ultimate focus. - Conduct all activities in accordance with all relevant policies, procedures and compliance guidance. - Educate external medical stakeholders based on patient care gaps and aligned to medical strategy with the goal of enhancing understanding of disease state and guideline-based care and improve overall patient care. - Achieve leadership-defined expectations regarding the number of external medical stakeholders engaged. Qualifications - MD or DO Degree required. - 4+ years of relevant experience required. - Subject matter expert recognized across internal and external stakeholders. - Demonstrate a breadth of diverse leadership experiences and capabilities including the ability to influence and collaborate with peers and create business impact. - Demonstrate excellent oral and written communication skills. - Demonstrate excellent interpersonal skills: ability to understand and respond to multiple external and internal stakeholders’ demands and manage and handle conflict constructively. - Manage a significant volume of projects developed in a remote environment, while exhibiting the ability to prioritize, successfully implement, and demonstrate excellent judgment skills and work in a continuous improvement environment. - Work within a matrixed, multi-disciplinary team to foster strong Pfizer/external medical stakeholder professional relationships which are aligned with Pfizer Medical objectives. - Effectively manage through and lead change in an ever-changing and evolving external health care environment. - Demonstrate change agility; be flexible to new opportunities (e.g. new therapeutic areas) and adaptable to organizational change. - Problem-solve and network enterprise wide as appropriate to identify solutions. - Collaborate effectively and demonstrate leadership and teamwork with peers, internal stakeholders and external medical stakeholders that inspires alignment and partnership on a shared vision or strategy. - Be a self-starter, be accountable, and have a sense of urgency in delivering results that have medical impact and yield a positive external medical stakeholder experience. - Maintain self-awareness and continually choose behaviors and responses based on how it impacts one’s own and others’ performance and engagement. - Demonstrate clinical and technical skills. - Rapidly adopt and utilize new digital technology and other resources with medical external medical stakeholders and record medical interactions. Requirements - Familiarity with internal/external SOPs/Rules/Regulations regarding Pfizer/external medical stakeholder interactions and relationships, etc. - Previous Field Medical experience. Benefits - The annual base salary for this position ranges from $230,900.00 to $384,800.00. - This position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 25.0% of the base salary. - Eligibility to participate in our share-based long-term incentive program. - Comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. - Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution. - Paid vacation, holiday and personal days, paid caregiver/parental and medical leave. - Health benefits to include medical, prescription drug, dental and vision coverage.