Pfizer, S.A. de C.V
Oncology Medical Writer (Senior Manager/Associate Director)
Pfizer, S.A. de C.V, Long Island City, New York, United States, 11101
Oncology Medical Writer (Senior Manager/Associate Director) We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.
Before applying for this role, please read the following information about this opportunity found below.To fully realize Pfizer’s purpose – Breakthroughs that change patients’ lives – 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.What You Will Achieve Your strong documentation skills will be an asset for the team. You will help us draft manuscripts on clinical studies and scientific reports for submission to regulatory agencies or in-company use. You will also help with summaries, monographs, comprehensive reviews, scientific exhibits and projects requiring skill in medical communication.Your ability to develop and manage plans will facilitate achieving objectives, interpreting internal and external business challenges and recommending best practices for improvements. While managing complex project environments, you will be able to anticipate and troubleshoot roadblocks and influence teams to achieve targets for the division. Through your expertise and extensive knowledge, you will be able to foster a culture that promotes innovation and thrives on doing better for patients and healthcare.How You Will Achieve It
Develop ideas and lead/co-lead complex projects across business units and develop plans to achieve objectives.Drive document strategies and messages in a collaborative way with relevant project team subject matter experts.Suggest changes to document processes or templates to improve quality and efficiency.Collaborate with clinicians, statisticians and clinical scientists to author protocols.Independently plan and prepare key clinical documents by organizing, analyzing, and interpreting scientific clinical and statistical data.Utilize a balanced approach to problems, using flexibility and persistence as appropriate.QualificationsMust-Have
Bachelor's Degree7+ years' experienceMedical writing experience in the pharmaceutical or biotech industryDemonstrated ability to interpret and apply these guidelines to document writingComprehensive understanding of the drug development process and regulatory knowledgeExcellent project management skills to organize work and handle multiple projects at the same timeAbility to work independently with minimal supervision, multi-task and work effectively under pressureExperience with software commonly used to present and analyze data, such as Word, PowerPoint, ExcelOncology writing experience strongly preferredNice-to-Have
Master's degreeBenefits at Pfizer Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues. Our Pay for Performance Philosophy and Practices reward colleagues based on the contributions they make to our business.Our Competitive Benefits Programs help our colleagues by:Promoting Health and Wellness
to help colleagues maintain and improve their physical and mental wellbeing.Strengthening Colleagues’ Financial Security
by providing company contributions to retirement plans, life insurance and financial planning education to help colleagues achieve their financial goals.Providing Benefits and Time off for the Moments that Matter
to ensure Pfizer colleagues have the time away from the office to recharge, recover and return to work as the best version of themselves.And so much more , depending on your country and site.
#J-18808-Ljbffr
Before applying for this role, please read the following information about this opportunity found below.To fully realize Pfizer’s purpose – Breakthroughs that change patients’ lives – 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.What You Will Achieve Your strong documentation skills will be an asset for the team. You will help us draft manuscripts on clinical studies and scientific reports for submission to regulatory agencies or in-company use. You will also help with summaries, monographs, comprehensive reviews, scientific exhibits and projects requiring skill in medical communication.Your ability to develop and manage plans will facilitate achieving objectives, interpreting internal and external business challenges and recommending best practices for improvements. While managing complex project environments, you will be able to anticipate and troubleshoot roadblocks and influence teams to achieve targets for the division. Through your expertise and extensive knowledge, you will be able to foster a culture that promotes innovation and thrives on doing better for patients and healthcare.How You Will Achieve It
Develop ideas and lead/co-lead complex projects across business units and develop plans to achieve objectives.Drive document strategies and messages in a collaborative way with relevant project team subject matter experts.Suggest changes to document processes or templates to improve quality and efficiency.Collaborate with clinicians, statisticians and clinical scientists to author protocols.Independently plan and prepare key clinical documents by organizing, analyzing, and interpreting scientific clinical and statistical data.Utilize a balanced approach to problems, using flexibility and persistence as appropriate.QualificationsMust-Have
Bachelor's Degree7+ years' experienceMedical writing experience in the pharmaceutical or biotech industryDemonstrated ability to interpret and apply these guidelines to document writingComprehensive understanding of the drug development process and regulatory knowledgeExcellent project management skills to organize work and handle multiple projects at the same timeAbility to work independently with minimal supervision, multi-task and work effectively under pressureExperience with software commonly used to present and analyze data, such as Word, PowerPoint, ExcelOncology writing experience strongly preferredNice-to-Have
Master's degreeBenefits at Pfizer Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues. Our Pay for Performance Philosophy and Practices reward colleagues based on the contributions they make to our business.Our Competitive Benefits Programs help our colleagues by:Promoting Health and Wellness
to help colleagues maintain and improve their physical and mental wellbeing.Strengthening Colleagues’ Financial Security
by providing company contributions to retirement plans, life insurance and financial planning education to help colleagues achieve their financial goals.Providing Benefits and Time off for the Moments that Matter
to ensure Pfizer colleagues have the time away from the office to recharge, recover and return to work as the best version of themselves.And so much more , depending on your country and site.
#J-18808-Ljbffr