Pfizer

Data Scientist

• Contribute to moderately complex projects, managing time effectively to meet targets and develop short-term work plans
• Take on the role of Data Manager for clinical trials, overseeing Data Monitoring and Management (DMM) activities
• Collaborate with partners and colleagues to ensure operational excellence and apply standards while developing data cleaning reports
• Maintain high standards across all DMM deliverables and ensure data quality and completeness as specified in the Data Management Plan
• Document and share lessons learned during studies to promote cross-study learning
• Build strong relationships with local and global subject matter experts (SMEs) to leverage their expertise in systems and processes, proactively identifying issues and developing solutions

Senior Associate, Senior Data Manager, Clinical Data Sciences

Business Analyst

• Support the compilation of data from various sources
• Generate and maintain dashboards, business scorecards, and reports
• Influence decision-making through data-driven insights
• Investigate new technologies for better business efficiency
• Contribute as a member of system change control boards
• Lead process development by translating business requirements
• Serve as the primary point of contact for label exchange activities
• Monitor and resolve discrepancies ensuring alignment with safety and regulatory commitments
• Maintain the integrity and accuracy of labeling and artwork pan-portfolio intelligence data

Senior Business Analyst, Labeling

Compliance

• Works independently to manage key site changes with regulatory impact from initiation through submission to implementation and manages product holds for pending market activities.
• Exercises own judgement leveraging knowledge and experience with minimal assistance from Management.
• Provides peer leadership to mentor and develop other colleagues.
• Supports license renewals in global markets, through the development of support strategies, and the preparation and submission of site documents to Pfizer colleagues globally with emphasis on supply equity.
• Develops and reviews site responses to queries received from global Health Authorities.
• Ensures communication of regulatory approvals to appropriate site personnel and PC1 customers.
• Manages communication between PC1 customers, site SMEs and Regulatory Affairs, works with Reg Affairs to resolve issues, holds meetings with strategists and PC1 customers to discuss open regulatory impact assessments for proposed changes.
• Completes impact assessments for key site change requests to document potential for regulatory impact and manage implementation.
• May complete the CNM and/or PC1 customer section of Annual Product Reviews.
• Manages Pfizer support of PC1 US annual report process.
• Upkeep and development of department SOPs, monitoring alignment with regulations and Pfizer Quality Standards.

Regulatory Change Management Project Leader – 12 Months

Director

• Lead and coordinate the development and execution of multiple studies for small molecule and/or novel biological therapies
• Independently lead the development of the clinical protocol
• Participate as an individual contributor on clinical study teams to meet enrollment and study delivery timelines
• Collaborate with other functional disciplines (e.g. Clinical Operations, Global Development Leads/Medical Monitors, Biostatistics, Data Management, Clinical Pharmacology, and Digital Medicine)
• Hold colleagues accountable, manage conflicting priorities with stakeholders, and exhibit strong clinical judgement
• Lead preparation of study related documents and contribute to preparation of other study related documents
• Develop and implement clinical data review strategy
• Serve as technical resource for clinical issues raised by internal and external collaborators, investigators, consultants and contractors
• Support and assist in the development of publications, abstracts, and presentations

Director, Clinical Development Scientist – Early Clinical Development

• Participate in CDIS activities including data review and query management.
• Assist with quality database design including documentation, testing, validation, and implementation of clinical data collection tools, CRF and non-CRF, using an electronic data capture (EDC) system and/or other data collection systems.
• Ensure work carried out in accordance with applicable SOPs and working practices.
• Ensure the required study-specific CDIS documents in the Trial Master File (TMF) are of high quality and are filed contemporaneously to support downstream inspection and submission readiness activities.
• Ensure operational excellence in collaboration with Data Manager and Clinical Data Scientist for application of standards, data acquisition, proactive data review and query management, data cleaning, e-data processing, data access and visualization, DM metrics reporting, database release, and submission related activities.

Data Manager

• Own and lead the US HCP strategy for XTANDI
• Identify, develop, and execute HCP strategies and tactics that maximize brand performance
• Act as Promotional Lead, driving messaging and differentiation
• Partner closely with Medical, Sales, and Analytics to ensure promotion is impactful
• Work with analytics colleagues to monitor performance trends
• Partner cross functionally to align HCP strategy with broader lifecycle considerations
• Develop and deliver presentations for senior leadership
• Own the HCP AOR agency relationship, including budget oversight

Director, US XTANDI HCP Lead

Communications

• Lead the offshore Medical Communications and Content Solutions (MCCS) team accountable for creating global medical channel content across all Pfizer therapeutic areas and medicines, including abstracts, manuscripts, congress presentations, plain language summaries, slide decks, social media posts and other types of external-facing medical content.
• Lead the off-shore Medical Information & Review Team.
• Sponsor and lead enterprise level teams that define the strategic direction for global medical content development, review, and medical information capabilities.
• Lead the development and implementation of the global medical content production strategy which includes offshoring, agency consolidation and technology enabled in-house content creation and localization across Global/US and International.
• Optimize publications and medical content development capabilities for all relevant medical affairs content.
• Elevate Gen AI fluency & implementation and drive development of tools and processes, including new generative AI technology platforms.
• Make and influence high impact decisions that may entail strategic risk or business opportunity.
• Monitor progress and manage stakeholder expectations around impact of outsourcing, change management, risks, and mitigation strategies.
• Promote best practices and organizational expertise in Medical Review skills & capabilities across Medical and Promotional Content Reviews.
• Oversee, plan, and project resource utilization and allocation to meet the publications and medical content needs of the Medical Affairs Category Teams.

Global Medical and Scientific Communications Capabilities Hub Team Lead

Marketing

• Joining the Velsipity team means stepping into a high‑visibility, fast‑moving brand environment where you can directly shape the trajectory of a major growth brand, elevate UC care, and contribute to a collaborative, ambitious, and supportive marketing organization making a real impact for patients.
• Lead the end‑to‑end development and execution of critical consumer initiatives
• Ensure seamless pull‑through of the new creative platform into a cohesive, high‑impact experience across priority channels such as the website, point of care, patient education (print), and pre‑initiation touchpoints.
• Partner with agency and internal teams to ensure a smooth transition with minimal disruption

Senior Consumer Marketing Manager, VELSIPITY

• Develop and execute US go-to-market strategies for Pfizer’s Pain Management portfolio
• Drive revenue/margin growth and develop pricing strategies
• Work with sales and internal leadership to develop key programs
• Manage P&L responsibilities including net sales and gross margin
• Engage leadership on strategic issues and project plans
• Collaborate with Field Sales and cross-functional partners for market activities
• Develop strategies for contracting, pricing, and supply management
• Communicate strategies and updates to team and leadership
• Identify relevant insights to integrate into molecule plans
• Interact with external partners to discuss market trends and volume requirements

Director, US Marketing – Pain Management

Business Operations

• Report to the US Vaccines Field Sales Operations Lead
• Provide a broad range of operational support to the Vaccines business unit
• Identify innovative solutions to simplify processes
• Lead operational projects for US Vaccines Sales
• Serve as operational support lead and point of contact for cross-functional partners
• Manage operational tasks efficiently
• Facilitate field insight groups as needed
• Collaborate with various teams to resolve issues efficiently
• Plan key meetings including launch meetings and leadership training classes

Senior Manager, Business Ops – Vaccines Sales

Manager

• Lead the development of the HTA, Value & Evidence Strategy to support the access values of assets in close partnership with the cross-functional matrix team
• Work closely with PRD, CMAO, WRD, and commercial to ensure that their access evidence/HEOR needs are met
• Work with cross-functional teams to ensure an aligned value and evidence plan at the Global level
• Develop real world evidence generation strategies and lead the design and execution of studies (e.g. treatment patterns, real world effectiveness, burden of illness studies, epidemiology studies, etc) to generate evidence to support brand competitive differentiation and value proposition
• Lead the execution of clinically relevant and scientifically valid, cutting edge HEOR studies and projects (including non-interventional studies, registries, etc.) in alignment with the global HEOR strategy catered to diverse stakeholders (regulators, payers, patients, physicians and policy makers)
• Lead the development of appropriate data dissemination plans and communicate in a timely manner
• Remain fully compliant to all Pfizer SOPs (Standard Operating Procedures).

Senior Manager, HTA, Value and Evidence, Medical Dermatology

• Lead the development of the evidence generation strategy to support the value of Sick Cell Disease assets
• Lead the coordination of input from local country/regional teams on evidence needs
• Lead the design and execution of global HEOR studies
• Lead the timely development of launch deliverables including comprehensive trial-based evidence
• Provide strategic input into clinical trial designs
• Partner with internal stakeholders to ensure appropriate dissemination of HEOR materials
• Develop strategic partnerships and research collaborations with key external experts

Director, HTA, Value & Evidence – Rare Disease

• Plan and perform care gap advanced analytics and segment HCPs and KOLs using real world data sources as input.
• Support Care Gaps & Segmentation Team Leader in strategic and tactical planning with regards to medical analyses.
• Collaborate with Care Gaps & Segmentation Team Leader to communicate generated insights.
• Provide mentorship & coaching to Data Scientists & Data Engineering.
• Leverage cross-team collaboration and asset-specific experience to develop and disseminate analytical best-practices in conducing care gap analyses and HCP segmentation.
• Proactively identify future opportunities, such as data inputs, innovative analytical tools, and capability-building initiatives to enhance the impact and adoption of care gap and segmentation solutions.
• Prepare and maintain datasets for on-going high-complexity analytical needs, in collaboration with data engineers, including flagging data issues & advising on required solutions.
• Own the end-to-end process of integrated care gaps analyses, including strategic planning, identifying data input required (e.g., claims data for unmet need analysis), and effective visualization / insight generation for users.
• Plan, generate and perform asset-specific care gap analyses to guide Medical Affairs activities using advanced techniques such as predictive models, machine learning, probabilistic causal models, and unsupervised algorithms.
• Create asset-specific HCP segments, maps, and prioritizations, across multiple dimensions including care gaps, to guide channel mix/activation, content creation, and MSL activity in Anchor countries.

Senior Data Scientist, Medical Analytics, Care Gaps, Customer Segmentation

• Plan and perform care gap advanced analytics and segment HCPs and KOLs using real world data sources as input.
• Support team Product Manager in strategic and tactical planning with regards to medical analyses.
• Collaborate with team Product manager to communicate generated insights.
• Prepare and maintain datasets for on-going analytical needs in collaboration with data engineers.
• Flag data issues to data engineers and advise on required resolution.
• Develop integrated care gaps analyses planning including data input required.
• Plan, generate and perform asset-specific care gap analyses using advanced techniques such as predictive models, machine learning, probabilistic causal models, and unsupervised algorithms.
• Create asset-specific HCP segments, maps, and prioritizations to guide channel mix/activation, content creation, and MSL activity in Anchor countries.
• Highlight missing data inputs needed to conduct analytics (e.g., claims data for unmet need analysis).
• Ensure visualization / insights generation from data is easily accessible and understandable for users.

Data Scientist, Medical Analytics, Care Gaps, Customer Segmentation

Vice President

• Provide strategic and operational leadership for all biometrics activities supporting Oncology drug development
• Ensure high-quality statistical strategy, study design, analysis, and interpretation
• Lead global teams spanning biostatistics and related biometrics capabilities
• Partner closely with Clinical Development, Regulatory, Safety, Clinical Pharmacology, and Translational Medicine
• Ensure statistical integrity, regulatory compliance, innovation, and efficient execution