Medical Affairs Scientist (m/w/d) für die Sichelzellerkrankung, Region Süddeutschland
Medical Affairs Scientist (m/w/d) f r die Sichelzellerkrankung, Region S ddeutschland Weltweit arbeiten die Mitarbeiter:innen von Pfizer gemeinsam daran, die Gesundheit eines jeden Einzelnen berall zu verbessern.$76k-105k yearly est.2d ago
Fullstack Engineer
There will be a close collaboration required with Levi's Global Product, and Technology Teams in San Francisco, but also with the specialists in the US and European region.The successful candidate will have a winning combination of technical skills, passion and interest for SEO, collaborative mindset and an entrepreneurial spirit. From my perspective: its an SEO engineer role (SEO, SEM, Web Analytics) with some programming implementation in VueJS and possible substitution with ReactJS. ChatGPT SEO Engineer will be responsible executing technical enhancements based on business growth objectives and in collaboration with key business partners.$133k-170k yearly est.13d ago
Director, Drug Product Lead, Seasonal mRNA Vaccines
Pfizer Global Supply (PGS) is at the heart of fulfilling Pfizer's purpose as we work to make sure customers and patients have the medicines they need, when they need them. Pfizer's purpose is to deliver breakthroughs that change patients' lives. As the Drug Product Lead, you will build and maintain strong matrix relationships with key partners in GTE, Supply Chain, Manufacturing Sites, Launch Excellence, PGS Sites, Biotherapeutics Pharm Sci, Quality, Procurement, and Regulatory CMC. As the Director, Drug Product Lead seasonal mRNA Vx for Vaccines in Biotech and Sterile Injectable Technology, you will be accountable for the seasonal mRNA Vx Drug Product (DP) processes lifecycle and leading the matrix DP teams for Pfizer's seasonal mRNA vaccine assets (Ex: mRNA Flu).$86k-121k yearly est.9d ago
I&I Senior Health & Science Sales Specialist, Rheum/GI Poughkeepsie, NY GI1
Present terms of sale of product or existing contract terms where appropriate and with approved language; proactively answer on-label questions; proactively introduce customers to future state Pfizer on-demand portal (Galaxy) with access to appropriate targeted cont$74k-103k yearly est.9d ago
The CTA-SM may be assigned as a Hub Submission Manager to meet business demands. Manager Drives global submission management activities for their assigned assets. Provides an interface to Regulatory and GPD partners within designated Business Units, offering project leadership and expertise in the logistics involved with execution of regulatory CTA submissions to regional partners and selected Health Authorities.The CTA Submission Manager (CTA-SM) is accountable for working with contributing business lines to lead operational submissions execution for designated CTAs.$108k-145k yearly est.9d ago
Director - Process and Innovation Lead
Product License Maintenance Data Sciences (PLMDS) is a multi-functional organization in Global Regulatory Operations/Global Regulatory Sciences.
The PLMDS Process and Innovation Lead is responsible for a range of research, development, business and process-related initiatives across the PLMDS organization.
The role is broad, covering a wide range of supportive disciplines, and colleagues within the role will specialize in one or more areas depending on business need:
The role is a key driver of innovative thinking in PLMDS, helping create a virtual culture of risk-taking and creativity, and works closely with the Head of PLMDS Functional Leads, PLMDS Managers and CDM Managers to execute cutting edge innovations and transformative projects.
Leadership of large and medium scale projects to improve efficiency, quality or cost, with equal focus on effective implementation of these projects, using advanced change management and knowledge management techniques.
Subject matter expertise in general business process, this role will have awareness of a local regulations. The role sponsors, coordinates and directs process forums and associated continuous improvement efforts to ensure PLMDS processes are efficient and globally consistent.
Championing data quality, verification, connectivity and governance to facilitate understanding and contextualize areas of opportunity. The role has expert knowledge of PLMDS metadata and systems, and their relationship to wider business process and policies, and acts as a facilitator to other support lines to leverage expertise into PLMDS to resolve challenges.
Development of products, services or approaches which support the smooth functioning of PLMDS and wider business value. Such support may include partnership with Business Operational functions to facilitate full transparency of capital opportunities across the organization, predictive analytics which enhance forecasting ability, and practical return-on-investment (ROI) calculation techniques to support PLMDS. This support is highly integrated and tailored to meet the needs of PLMDS functions so that the model is optimized to meet customer needs.
Acting as a Mentor/Coach to peers/colleagues delivering projects including project management, advanced change management and knowledge management techniques.
He/She will have a global view of PLMDS functions, is comfortable working across a range of deliverables from early research investigations, through project design/management, to effective implementation. The incumbent is both an advocate for innovation as well as a champion for quality and delivery.
In addition, this role may include monitoring trends and policy positions in the global regulatory environment that impact PLMDS. Partners with Policy Intelligence to provide seminal analyses of these regulatory trends and communication to internal stakeholders.
JOB RESPONSIBILITIES
Program management of multi-regional technological, behavioral and process change activities, with particular emphasis on transformational projects.
Leads selected roadmap projects, working with other functions to ensure effective implementation of final solutions.
Participant/lead on Steering groups across selected geographies (Americas, Europe, Asia, Emerging Markets) to progress strategic change related to Labeling processes
Where appropriate acts as subject matter expert on development of standards supporting Industry associations, regulatory agencies (as support to PPLS teams), vendors, and in-licensing partners
Accountable for associated PMO activities for selected roadmap projects including but not limited to provision of metrics dashboards, ROI calculations, Hypothesis testing, predictive modelling, and impact assessments.
Review draft and final regulatory agency regulations, guidelines and regulatory policies. Identify the strategic impact of these regulatory documents to PPLS.
Development of effective knowledge management and communication techniques to organize and deliver training either personally or via network of trusted experts
Prepare environmental analyses to identify emerging regulatory trends and likely future scenarios resulting from emerging trends. Educates PPLS and stakeholders on key priorities, trends, and changes in the regulatory environment.
Promotes innovation and takes appropriate risks to challenge the status quo, resulting in enhanced processes; takes appropriate risks to develop innovative ideas/ processes/products.
Fosters an environment that thrives on curiosity
Identifies innovative concepts, translates into processes within PPLS and recommends courses of action to senior leaders that impact PPLS and the wider business.
Working with the PLMDS LT, develops vision, strategy, and performance objectives for the end-to-end processes.
Acts as SME Point of Contact with Information Management (IM), Business Operations Center of Excellence (CoE), Regulatory Policy and other functions on behalf of PPLS.
Exercises foresight and judgment utilizing comprehensive breadth of knowledge and prior work experience
Acts independently on self-initiated projects and leverages knowledge from others related to overall objectives, strateg
y, critical issues and policy matters
QUALIFICATIONS / SKILLS
Indicate qualifications and skills that are necessary for performance of responsibilities including: education, relevant experience, licenses, certifications and other job-related technical and managerial skills.
Proven fluency with the use of soft skills and ability to adapt core project management skills successfully within a dynamic line environment.Extensive business experience at required level to enable thorough understanding of the responsibilities associated with strategic pursuit and tactical application of evolving business processes Ability to transform ambiguous situations/discussions into structured outcomes Management of change in partnership with key stakeholders Proven leadership and delivery to time and quality driving highly complex projects to meet evolving business needs.Mastery of processes, tools and techniques for planning and monitoring multiple complex projects to established deadlines. Excellent knowledge of tools used to design processes and process flows, etc.Proven aptitude in project management and process engineering/re-design Leadership, project management, and highly skilled adaptive verbal and written communication skills in relating to colleagues and associates both inside and outside the organization, across various cultures.Demonstrated accountability, and excellence in interpersonal, communication, negotiation, influencing, and problem-solving capabilities.Demonstrated knowledge of drug development processes, regulatory codes/guidance's, and technologies across ICH regions Demonstrated ability to work with or lead a team in a matrix structure.Experience with XML, Document Management, regulatory milestone reporting tools Ability to synthesize and communicate complex information and analyses to a variety of audiences in both verbal and written format Ability to extract critical information and prepare succinct summaries of regulatory documents, including assessment of the potential impacts to Pfizer.Ability to conduct regulatory metrics analyses, and regulatory trending and impact analyses.Ability to easily navigate information databases and health authority websites to gather necessary information.Understanding the global regulatory environment and its impact on BU strategies.Background in medical or technical writing Highly skilled at identifying the potential provided by innovative thinking, concepts or technologies and translating these into opportunities across the spectrum of labeling processes Comfortable operating and leading in a risk-taking environment, striving for transformational gains while conscious of regulatory risks in different regions. Capable of cutting through complexity to deliver simple solutions with decisiveness and clarity.Anticipating internal/external business and regulatory/ compliance issues that impact PLMDSHave foresight and judgment in complex decisions and troubleshoots in ambiguous situations in PLMDSHave the ability to influence senior management decisions that impact business direction
Education:
Bachelor's Degree or equivalent preferred Advanced academic qualification/degree is desired but not required.
Experience:
Strong experience in global/multi-national pharmaceutical environment, including direct experience either in Labeling, Regulatory Submissions, or Regulatory Affairs role. Experience in ability to function autonomously at senior levels and in a matrix team environment a must.Experience in interpreting and applying global and local regulatory guidance around labelling and associated supportive documentation are desirable but not required.Experience in identifying, driving and implementing innovative solutions
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Purpose
Breakthroughs that change patients' lives... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.
Digital Transformation Strategy
One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.
Flexibility
We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let's start the conversation!
Equal Employment Opportunity
We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms - allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.
DisAbility Confident
We are proud to be a Disability Confident Employer and we encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments necessary to support your application and future career. Our mission is unleashing the power of our people, especially those with unique superpowers. Your journey with Pfizer starts here!
Regulatory Affairs
#LI-Remote #LI-PFE$82k-107k yearly est.9d ago
Representante de Salud Cuidado Primario (Monterrey)
Comprometido a Un solo Pfizer$39k-53k yearly est.2d ago
Director, Epidemiology Scientist
GME colleagues are located in Collegeville, PA and New York but Pfizer is flexible regarding remote work for the right candidate. The Director, Epidemiology Scientist position provides an opportunity for an experienced epidemiologist to play an essential role in advancing the generation of real-world evidence and its application to drug development. Pfizer's Global Medical Epidemiology (GME) group conducts observational, epidemiologic research, often using large healthcare databases, to generate a better understanding of disease context and medical outcomes and improve medical decision-making for Pfizer medicines development. The incumbent will also develop and adopt innovative pharmacoepidemiologic methodologies and contribute thought leadership internally and externally regarding Pfizer's understanding of disease epidemiology/ pharmacoepidemiology to support decision-making across portfolios. The Director, Epidemiology Scientist will also partner with internal and external stakeholders on the design and conduct of epidemiologic research to inform clinical development programs and to support regulatory submissions to the FDA, EMA and other agencies globally. GME's value is based on deeper understanding of disease that improves quality and precision of Pfizer medical decisions.$156.9k-261.5k yearly2d ago
Coordinate tasks and drive actions across teams within Pfizer and with external partners in a global environment. We are seeking a highly motivated individual to join the Global Digital Operations (GDO) team (within Pfizer's Platform DevOps organization) as a Platform Embedded Operations Analyst. The Platform DevOps (PDO) team are accountable for the platforms at Pfizer that allow the creation, configuration, launch, and support of all externally facing digital (web, mobile, omni-channel, & device) products, services, and experiences, servicing all external customer types at Pfizer.$77k-104k yearly est.9d ago
Health Representative
Submits reports regarding calls made to doctors and chemists to his Health Representative Manager on the prescribed forms. Follows the plans to achieve objectives assigned for increased prescription flow from identified doctors and reports his findings periodically to his Health Representative Manager. Position Title : Health Representative Reports To : Health Representative Manager Forwards technical queries raised by his doctors to the Medical Division for clarification with intimation to the Health Representative Manager. Makes professional presentations using selling skills to listed doctors on the approved indications of Pfizer products with a view to increase prescriptions.$41k-52k yearly est.9d ago
Rare Disease Field Medical, Outcomes & Analytics Director, MD
The Rare Disease Field Medical, Outcomes & Analytics colleague is responsible for educating customers on the clinical and economic impact of Pfizer medicines and products.$185k-270k yearly est.2d ago
All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Promote products in competitive market and launch new products Strong knowledge of high science disease states, therapeutic areas, and products Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) Generate demand for Pfizer products in assigned accounts Strategic account selling and management skills. Pfizer, a global leader in the biopharmaceutical industry, is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives. The OAS plays a critical role in increasing Pfizer's brand with high-value target customers by linking an insightful assessment of the account and/or business landscape with a strong understanding of Pfizer's products and resources.$51k-69k yearly est.2d ago
Increase expertise amongst Pfizer statisticians and scientists through dissemination of new RWD analysis and modern analytic methodologies and training on software to implement these approaches.Collaborate with development teams by the development and implementation of techniques based on state-of-the-art research.Take ownership of projects and liaise with team members as appropriate and may oversee the work of contractors. Provide statistical leadership and technical support for Pfizer projects involving real world data (RWD).$96k-133k yearly est.9d ago
Trade Marketing Rep. Virtual - Upjohn
$55k-82k yearly est.9d ago
Cybersecurity Awareness Associate
The overall goal of the security awareness and education program is to reduce information security risk by ensuring that all colleagues and leadership comprehend security risks and policies and apply good information security practices with respect to Pfizer data and information technology systems. The Cybersecurity Awareness Associate is accountable for obtaining the security awareness requirements and needs of Pfizer's research and product development divisions. The Cybersecurity Awareness Associate will also be accountable for evaluating effectiveness of techniques and resources as appropriate.$71k-111k yearly est.2d ago
Director MolecDiscovery, RNA Therapeutics & Synthetic Biology Innovation
On Premise colleagues work in a Pfizer site because it's needed to get their job done. The role oversees a highly motivated group of scientists with diverse expertise within the Biomedicines Design (BMD) group, Pfizer's large molecule discovery unit. The Director of RNA Therapeutics and Synthetic Biology Innovation will provide scientific and strategic leadership for RNA Therapeutic discovery and novel modality platform development.$97k-137k yearly est.33d ago
Senior Manager - Solution Engineer
It is your hard work and focus that will help in making Pfizer ready to achieve new milestones and help patients across the globe. Pfizer's digital and data first' strategy focuses on implementing impactful and innovative technology solutions across all functions from research to manufacturing. You will support a range of activities, such as coding, testing, debugging, documentation, implementation and maintenance of software applications for Pfizer.$87k-118k yearly est.9d ago
Associate Director, Biostatistics
$118k-157k yearly est.9d ago
USA Sales Talent Community
These laws and regulations require Pfizer to pro + Must live within a commutable distance to assigned Pfizer Connect Center location Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. The Pfizer Connect Health & Science Representative (PCHR) is responsible to increase product awareness, educate customers and attain the goals of their Business Unit through fully remote / virtual customer interactions. ** All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Pfizer, a global leader in the biopharmaceutical industry, is continuously seeking toptalentwho are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives. Pfizer recruiters may reach out with potential opportunities.$56k-74k yearly est.4d ago
Neuroscience Health & Science Professional - Palo Alto, CA
All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Pfizer is advancing in Neuroscience, and an integral part of the Migraine Team's mission is to promote a breakthrough therapy for patients suffering from migraine. Pfizer, a global leader in the biopharmaceutical industry, is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives.$44k-58k yearly est.9d ago
