Director

• Develops the headquarters therapeutically aligned strategic plan, executes strategic initiatives and assists in planning of key performance indicators (KPI), goals and tactics that flow from evolving Value and Implementation priorities, and internal and external factors
• Executes and implements patient innovation and engagement activities through incorporation of the patient voice into internal strategy development and decision-making across our company
• Supports efforts to gather and include patients’ and advocates insights and perspectives throughout the product lifecycle
• Develop the headquarters therapeutically aligned strategic patient advocacy and educational plans
• Develop, manage, and support long-term PAO relationships through engagement and communication
• Serve in a liaison function to PAOs and patient arms of professional societies
• Facilitate engagement through active participation at national and regional congresses and successful implementation of meetings with PAO leadership and executive staff.
• Ensure compliance with existing company guidelines as they pertain to patient advocacy
• Navigates across internal and external stakeholders ranging from individual patients to highly networked patients and medical organizations
• Collaborates with key internal stakeholders to proactively develop and execute the global Value and Implementation plan
• Participates in external conferences, congresses, and industry consortiums to represent our company’s focus on the patient including speaking, presenting and authoring publications
• Ensures alignment with regional and country level related activities (patient, scientific, medical)
• Supports any division with needs relating to patient engagement or patient advocacy, including our Company's Research Labs, Human Health, our Company's Manufacturing division, IT, and others
• Develops the talent on the team and seeks opportunities to enhance their capabilities
• Tracks associated spend for activities and communicates with TA and Strategy Lead
• Tracks and reports impacts, findings and associated key metrics and measurements related to work

Associate Director, Scientific Patient Engagement and Advocacy Lead, Oncology

Administrative Assistant

• support the AVP of Marketing and their team in the US Respiratory Organization
• General Secretarial/Clerical duties constitute approximately 50% of job responsibilities
• Work requires the coordination and performance of multiple tasks while understanding the project principles and technical skills related to own work assignments
• Works in teams or independently as needed and as relevant to complete work assignments and various tasks
• Assists team with designated tasks on a prioritized basis and problem solves when appropriate
• Encourages self-sufficiency and trains team members as appropriate
• Calendar scheduling/planning of complex meetings; coordinating and scheduling complex multi-leg and international travel arrangements
• Looking proactively through calendars and identifying and communicating conflicts
• Completing complex/international travel expense reports in a timely fashion
• Communication Skills must be at a level to effectively interact with company executives and internal/external clients to maintain workflow
• Respects the importance of maintaining confidentiality and appreciation of professionalism
• Assists with interview scheduling and on-boarding of new hires
• Occasionally produces/completes various work assignments requiring advanced analytical ability, independent judgment, creativity, and problem-solving skills
• Occasionally develop reports, presentations, tables, graphs, correspondence and conduct light research using appropriate software
• Occasionally coordinates special projects.
• Periodic travel – 5%

Senior Administrative Assistant

Manager

• The FAM serves as the subject-matter expert on access related issues for healthcare professionals (HCPs) and healthcare organizations (HCOs)
• Analyze access issues and act as the local access resource for HCPs and other field force personnel and region management
• Where appropriate, coordinate with the access hub concerning individual patient cases including patient access and coverage assistance
• Collaborate cross functionally with Field Sales, Marketing, Market Access, Public Affairs, State and Government Affairs, Trade and Specialty Pharmacy Accounts
• Provide information and/or education to HCP accounts on patient access, including benefit verification, prior authorization process, appeals process, and patient support programs

Field Access Manager

• Lead the development and execution of global reimbursement strategies
• Oversee regional and local implementation to ensure timely access to diagnostic technologies
• Collaborate cross-functionally to shape evidence generation and payer engagement plans
• Guide regional teams to adapt global strategies to country-specific reimbursement pathways
• Oversee the development of global value dossiers and pricing frameworks
• Collaborate with Health Economics teams to develop economic models demonstrating value
• Implement training and awareness programs facilitating diagnostic reimbursement
• Identify emerging trends and payer policies impacting access and reimbursement strategies
• Work closely with clinical development, marketing, and policy teams for access optimization

Director – Global Market Access & Reimbursement, Precision Medicine

Clinical Research

• Evaluating pre-clinical and translational work for the purpose of generating early clinical development plans and Investigational New Drug applications
• Developing clinical development strategies for investigational or marketed drugs
• Planning clinical trials (designing, collaborating on operational plans, etc.) based on the clinical development strategy
• Medical oversight and overall conduct of ongoing or new clinical trials for investigational or marketed drugs
• Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication
• Participating in internal and joint internal/external research project teams relevant to the development of new compounds, and the further study of marketed compounds
• Supporting business development assessments of external opportunities

Senior Director, Clinical Research, Cardiovascular and Respiratory

• planning and directing clinical research activities involving new or marketed drugs in the Oncology Clinical Research group
• managing the entire cycle of clinical development, including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, publication, and presentation at national and international meeting
• providing internal scientific leadership for cross-functional areas supporting clinical trials
• interacting externally with key opinion leaders
• evaluating pre-clinical and translational work for the purpose of generating early clinical development plan and Investigational New Drug applications
• developing clinical development strategies for investigational or marketed agents
• planning clinical trials based on clinical development strategies
• monitoring and managing the conduct of ongoing or new clinical trials
• analyzing and summarizing clinical findings to support decisions regarding safety and efficacy

Distinguished Scientist, Clinical Research, Thoracic Malignancies

• Planning clinical trials (designing, collaborating on operational plans, etc.) based on the clinical development strategy
• Medical oversight and overall conduct of ongoing or new clinical trials for investigational or marketed drugs
• Analyzing and summarizing clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication
• Participating in internal and joint internal/external research project teams relevant to the development of new compounds, and the further study of marketed compounds
• Supporting business development assessments of external opportunities
• Actively engaging with other functional areas in support of study execution
• Working closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects
• Assisting the team in ensuring that other colleagues are informed of the progress of studies of our company and competitors' drugs
• Providing expert opinion, internally and externally, on relevant scientific questions within their responsibility
• Maintaining awareness of scientific developments within his/her area of expertise, in terms of new scientific findings, research methodologies
• Identifying scientifically and operationally strong investigators who can assist in the development of our company's investigational and marketed drugs
• Establishing communications with prominent clinical investigators in his/her particular field of interest
• Attending appropriate scientific meetings to maintain his or her competency and to maintain awareness of research activities in his/her area of responsibility
• Authoring detailed development documents, presentations, budgets, and position papers for internal and external audiences
• Facilitating collaborations with external researchers around the world
• Traveling on company business about twenty (20) percent of the time to manage future or ongoing clinical research projects.

Director, Clinical Research – Cardiovascular and Respiratory

• Provide program leadership in the development, commercialization, and transfer and sustained launch of medical devices and combination products globally
• Develop and execute strategic plans for technology transfer
• Provide Voice of Manufacturing input to early development teams
• Author and complete regulatory filing sections, and support response to questions and pre-approval inspections
• Secure early sponsorship and stakeholder alignment for projects and initiatives
• Ensure that all activities are conducted with the highest regard for safety, quality, and regulatory compliance

Associate Director, Drug/Device Combination Products Tech Transfer

Research Scientist

• support statistical programming activities for multiple and/or large/complex late-stage drug/vaccine clinical development projects
• development and execution of statistical analysis and reporting deliverables (e.g. safety and efficacy analysis datasets, tables, listings, figures)
• design and maintenance of statistical databases
• ensure that project plans are executed efficiently with timely and high-quality deliverables
• serve as the statistical programming point of contact and knowledge holder throughout the product lifecycle
• assurance of deliverable quality and process compliance
• effective deliverable development utilizing global and TA standards
• maintaining and managing a project plan including resource forecasting
• coordinating the activities of a global programming team that includes outsource provider staff
• membership on departmental strategic initiative project teams such as new statistical computing platform evaluation and development

Associate Principal Scientist, Statistical Programming – Late-Stage

Product Designer

• Develop and align UX strategy with business objectives
• Plan and implement user research strategies and methodologies
• Prepare research plans, discussion guides, and workshop materials
• Manage and prioritize UI/UX requests for the Digital Regulatory Docs Product Line
• Create schedules and allocate resources for prioritized UX activities
• Mentor other UX designers and researchers
• Conduct user research and usability testing, including heuristic evaluations, UI reviews, and user testing sessions
• Convert findings into recommendations and insights, summarize data, and present these to the product teams, product managers, and stakeholders
• Maintain and advocate for user-centered design standards
• Lead design thinking workshops and focus group sessions as necessary
• Create personas, storyboards, wireframes, prototypes, user flows, and visual mock-ups using current tools and processes
• Collaborate with product managers, engineers, and business stakeholders to develop user stories and ensure design meets requirements
• Participate in test planning and execution to verify that results meet business and non-functional requirements
• Work with product and engineering teams to create minimally viable products, analyze user feedback, and iterate designs
• Gather user feedback consistently to support data-driven product decisions
• Drive product design from concept to implementation
• Evangelize UX practices to other teams as well as the DRD product teams and colleagues

Senior Specialist, UX/UI Design

Account Manager

• Own the end-to-end performance of Vaccines Portfolio within ESI institutions
• Creating clinical demand among prescribers and end-users
• Securing and expanding budget headroom by influencing Purchase Committee
• Ensuring fast liquidation via robust demand Generation
• Drive scientific awareness and preference for our company's Vaccines
• Plan and execute HCP meetings, DAP for user departments & Consumer Awareness programs
• Map and engage institutional stakeholders
• Creating awareness among ESI beneficiaries through industrial area outreach programs
• Build strong relationships with ESI Corporation stakeholders
• Maintain institution & ESI dashboard and convert insights into monthly action plans
• Uphold company ethics, compliance, and scientific integrity in all interactions

Key Account Manager

Marketing

• Provide US payer input into Brand Marketing, Business Unit Leadership, Global Market Access Teams, our company Research Laboratories, Integrated Account Management, Legal, Compliance and Finance
• Active participation in the development of value evidence strategies; strong coordination with Outcomes Research / Value & Implementation (V&I)
• Leverage market and customer insights to shape market access strategies
• Develop payer customer segment strategy, promotional campaigns and value messaging for all US payer customer segments (health plan, PBM, ADAP, Medicaid, Medicare, federal, pharmacy, hospital and GPO)
• Develop pricing and contracting strategies for pipeline forecasting
• Support appropriate pull-through activities and payer related solutions for field sales and account management teams
• Work with Senior Specialist to develop and deploy resources to support managed care strategy

Associate Director – US HIV Payer Marketing

• Drives execution of the annual V&I plan with medical affairs colleagues from key countries and regions with a focus on the US.
• Acts as an empowered partner, making informed decisions with a strategic and agile mindset.
• Serves as the subject matter expert (SME) and connector across assigned therapeutic areas, translating global scientific platforms into actionable Medical Value Narratives (MVNs).
• Actively engages with country level stakeholders—including medical advisors, payers, and scientific leaders—to ensure strategic alignment and support local data generation, congress planning, and advisory boards.
• Serves as the medical representative within Product Development sub-teams (including Clinical, V&I, Commercial, Publications, and Label), leveraging the GMSA vision to drive strategic planning, outcome delivery, and tactical execution.
• Communicates pertinent information to stakeholders to inform and influence country and regional planning.
• Collaborates closely with V&I Outcomes Research (VIOR), Policy, Commercial, and Market Access teams to identify and address opportunities and barriers in key countries.
• Plays a pivotal role in bridging global strategy with local execution, ensuring that country-specific insights are integrated into the global V&I plans.

Global Director, Medical Affairs – Breast Cancer

• Analyze and interpret large volumes of structured and unstructured real-world patient level healthcare data, including but not limited to administrative claims, EHR/EMR, disease registry, and public-use databases.
• Develop machine learning algorithms and statistical/survival analysis models to extract meaningful insights and outcome research evidence.
• Work closely with stakeholders in outcome research, medical affairs, statistical programming, and IT functions to provide data-driven insights and solutions.
• Provide data science and real-world data expert inputs in internal and external collaborations.
• Present research findings in internal and external scientific congress meetings.
• Independently lead Real-World Evidence outcome research or advanced AI/machine learning research projects with minimum supervision.
• Stay current with the latest research and technologies in data science and machine learning.

Assoc Principal Scientist – Real World Evidence Capability Analytics

• Successful candidates will spend their first year in one of the following areas: (a) Global Clinical Development; (b) Global Regulatory Affairs and Clinical Safety; (c) Global Medical/Scientific Affairs
• Understand the role and methods of pharmaceutical research, participate in the writing of research protocols, conduct of clinical trials, safety monitoring, analysis of data and communication of study findings.
• Learn key regulatory policies and the procedures for interacting with health agencies (e.g. FDA).

MSD