Medical Information Content Specialist
Pfizer, S.A. de C.V, Poland, NY, United States
We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.
To fully realize Pfizer’s purpose – Breakthroughs that change patients and the world – we have established a clear set of expectations regarding what we need to achieve for patients and how we will go about achieving those goals.
Pfizer Research & Development serves as the beating heart of Pfizer's trailblazing product pipeline, the essence of our mission to bring life‑changing medicines to the world.
Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.
The Medical Information Content Specialist reports directly to the Medical Information Content Lead. The Medical Information Content Specialist is an extended member of the Global/US MI & Review Category Team supporting execution of scientific content strategies. Key responsibilities as directed by the Medical Information Content Lead and Medical Information & Review Category/Sub-Category Lead, US include, but are not limited to, researching, creating and updating US Product Scientific content within a designated portfolio/category(s) as the basis for responses to unsolicited medical inquiries. This role also interfaces closely with peer Medical Information & Review Scientists and Content Specialists/Scientists to support content related short/long duration assignments and collectively identify trends to measure content effectiveness and predict future content needs.
This role may involve peer review of other colleagues’ work; as well as providing literature searches and participating in medical information projects and initiatives.
Role Responsibilities Creates, maintains and reviews Scientific Response Documents (SRDs), Patient Response Documents (PRDs) and other related content supporting US products by ensuring responses are medically and scientifically accurate, high quality, timely, fair balanced, and meet customers’ needs. May be required to leverage GenAI as a supportive tool in content creation. Effectively manages relationships with colleagues to facilitate timely authoring and review.
Upon notification of US labelling changes; publication of new/or changes to major clinical practice guideline/recommendations; and in case of new congress materials becoming available - promptly assesses impact to content and implements necessary actions.
Serves as content expert for MI on responsible product(s) and associated category(s). Reviews and approves MI documents completed by others when appropriate.
Collaborates with colleagues and peer Medical Information & Review Scientists within their category team to routinely analyze inquiry data, establish content plan, develop clear understanding of customer needs and to ensure an open exchange of product information, business intelligence and best practices.
Performs high quality searches of internal data and medical literature in response to customer inquiries or as it relates to creating/updating MI content.
Aligns with local team and International MI & Review colleagues to ensure an open exchange of product information, content updates, business intelligence and best practices.
Exhibits thorough knowledge of MI work as well as a good understanding of other local MI stakeholders.
Maintains compliance with corporate and departmental trainings, Standard Operating Procedures (SOPs), implementation guidelines and US regulations related to the work being fulfilled. Provides an MI perspective on the development and revision of SOPs and Work Instructions (WIs) and other procedural documents related to content development, as necessary.
Proactively seeks new innovative solutions to improve MI processes and responses and to resolve problems.
Participates in or leads MI content and MI core‑related work assignments, projects/initiatives as needed.
May support Pfizer Medical Information US website content maintenance as needed. May participate in Medical Affairs product‑related meetings, trainings and launch excellence within assigned category(s) as needed.
Stakeholder Management The Medical Information Content Specialist is a customer‑focused role within Global/US Medical Information & Review that is primarily responsible for creating and maintaining scientific content to be used by colleagues in responding to unsolicited medical inquiries regarding Pfizer products. Note, that in general, the role does not involve direct contact with customers.
The role primarily has a local scope of responsibilities, requiring extended membership of Global/US teams and regular interaction with local MI & Review colleagues and interactions as needed with International MI & Review. In addition, it is likely that they will communicate on occasion with (for example) colleagues from Medical Affairs, Clinical Affairs, GCMC, Regulatory and Safety functions as their expertise relates to topics of scientific content.
The Medical Information Content Specialist will report into the Global/US Medical Information & Review organization, specifically to the Medical Information Content Lead, Poland.
Basic Qualifications Life science graduate preferred. PharmD, BS in Pharmacy, or MD/DO strongly preferred. Degrees from other medical disciplines also considered
Candidates with pertinent industry‑related experience and/or post‑graduate specialty/residency are desirable
Demonstrates strong English oral and written communication skills
1-3 years of medical information experience preferred
Demonstrates effective relationship management and customer orientation
Able to work in a fast‑paced environment with competing priorities
Proficiency with computer and software applications (i.e., Microsoft office)
Experience of working in a virtual environment would be advantageous
High level of proficiency in both written and spoken English required (C2 or Native Speaker)
Excellent verbal and written communication skills
Demonstrates keen analytical skills and attention to detail
Medical Writing experience advantageous
Ability to interpret and relay technical information
Proficient computer and keyboarding skills
Work Location Assignment: 100% Remote
Minimum Annual Base Salary: 129 750 PLN
Annual Bonus: 15%
Disability Inclusion Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here!
Pursuant to Article 24(6) of the Act of June 24, 2024 on the protection of whistleblowers, Pfizer Polska Sp. z o o. and Pfizer Trading Polska Sp. z o o. declare that they have adopted a joint internal reporting procedure, which, in accordance with the provisions of the aforementioned Act, is also available to persons applying for employment on the basis of an employment relationship or other legal relationship constituting the basis for providing work or services or performing functions. The content of the procedure is made available upon request sent to the contact person or to the email address sygnalisci-px@pfizer.com.
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To fully realize Pfizer’s purpose – Breakthroughs that change patients and the world – we have established a clear set of expectations regarding what we need to achieve for patients and how we will go about achieving those goals.
Pfizer Research & Development serves as the beating heart of Pfizer's trailblazing product pipeline, the essence of our mission to bring life‑changing medicines to the world.
Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.
The Medical Information Content Specialist reports directly to the Medical Information Content Lead. The Medical Information Content Specialist is an extended member of the Global/US MI & Review Category Team supporting execution of scientific content strategies. Key responsibilities as directed by the Medical Information Content Lead and Medical Information & Review Category/Sub-Category Lead, US include, but are not limited to, researching, creating and updating US Product Scientific content within a designated portfolio/category(s) as the basis for responses to unsolicited medical inquiries. This role also interfaces closely with peer Medical Information & Review Scientists and Content Specialists/Scientists to support content related short/long duration assignments and collectively identify trends to measure content effectiveness and predict future content needs.
This role may involve peer review of other colleagues’ work; as well as providing literature searches and participating in medical information projects and initiatives.
Role Responsibilities Creates, maintains and reviews Scientific Response Documents (SRDs), Patient Response Documents (PRDs) and other related content supporting US products by ensuring responses are medically and scientifically accurate, high quality, timely, fair balanced, and meet customers’ needs. May be required to leverage GenAI as a supportive tool in content creation. Effectively manages relationships with colleagues to facilitate timely authoring and review.
Upon notification of US labelling changes; publication of new/or changes to major clinical practice guideline/recommendations; and in case of new congress materials becoming available - promptly assesses impact to content and implements necessary actions.
Serves as content expert for MI on responsible product(s) and associated category(s). Reviews and approves MI documents completed by others when appropriate.
Collaborates with colleagues and peer Medical Information & Review Scientists within their category team to routinely analyze inquiry data, establish content plan, develop clear understanding of customer needs and to ensure an open exchange of product information, business intelligence and best practices.
Performs high quality searches of internal data and medical literature in response to customer inquiries or as it relates to creating/updating MI content.
Aligns with local team and International MI & Review colleagues to ensure an open exchange of product information, content updates, business intelligence and best practices.
Exhibits thorough knowledge of MI work as well as a good understanding of other local MI stakeholders.
Maintains compliance with corporate and departmental trainings, Standard Operating Procedures (SOPs), implementation guidelines and US regulations related to the work being fulfilled. Provides an MI perspective on the development and revision of SOPs and Work Instructions (WIs) and other procedural documents related to content development, as necessary.
Proactively seeks new innovative solutions to improve MI processes and responses and to resolve problems.
Participates in or leads MI content and MI core‑related work assignments, projects/initiatives as needed.
May support Pfizer Medical Information US website content maintenance as needed. May participate in Medical Affairs product‑related meetings, trainings and launch excellence within assigned category(s) as needed.
Stakeholder Management The Medical Information Content Specialist is a customer‑focused role within Global/US Medical Information & Review that is primarily responsible for creating and maintaining scientific content to be used by colleagues in responding to unsolicited medical inquiries regarding Pfizer products. Note, that in general, the role does not involve direct contact with customers.
The role primarily has a local scope of responsibilities, requiring extended membership of Global/US teams and regular interaction with local MI & Review colleagues and interactions as needed with International MI & Review. In addition, it is likely that they will communicate on occasion with (for example) colleagues from Medical Affairs, Clinical Affairs, GCMC, Regulatory and Safety functions as their expertise relates to topics of scientific content.
The Medical Information Content Specialist will report into the Global/US Medical Information & Review organization, specifically to the Medical Information Content Lead, Poland.
Basic Qualifications Life science graduate preferred. PharmD, BS in Pharmacy, or MD/DO strongly preferred. Degrees from other medical disciplines also considered
Candidates with pertinent industry‑related experience and/or post‑graduate specialty/residency are desirable
Demonstrates strong English oral and written communication skills
1-3 years of medical information experience preferred
Demonstrates effective relationship management and customer orientation
Able to work in a fast‑paced environment with competing priorities
Proficiency with computer and software applications (i.e., Microsoft office)
Experience of working in a virtual environment would be advantageous
High level of proficiency in both written and spoken English required (C2 or Native Speaker)
Excellent verbal and written communication skills
Demonstrates keen analytical skills and attention to detail
Medical Writing experience advantageous
Ability to interpret and relay technical information
Proficient computer and keyboarding skills
Work Location Assignment: 100% Remote
Minimum Annual Base Salary: 129 750 PLN
Annual Bonus: 15%
Disability Inclusion Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here!
Pursuant to Article 24(6) of the Act of June 24, 2024 on the protection of whistleblowers, Pfizer Polska Sp. z o o. and Pfizer Trading Polska Sp. z o o. declare that they have adopted a joint internal reporting procedure, which, in accordance with the provisions of the aforementioned Act, is also available to persons applying for employment on the basis of an employment relationship or other legal relationship constituting the basis for providing work or services or performing functions. The content of the procedure is made available upon request sent to the contact person or to the email address sygnalisci-px@pfizer.com.
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