Pfizer
Oncology Medical Writer (Senior Manager/Associate Director)
Pfizer, Long Island City, New York, United States, 11101
Oncology Medical Writer (Senior Manager/Associate Director) Locations: United States - New York - Remote, United States - Remote, Canada - Remote
Please make an application promptly if you are a good match for this role due to high levels of interest.Time Type: Full timePosted on: Posted YesterdayJob Requisition ID: 4917331Why Patients Need You Pfizer colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary expertise or investigating how to close gaps in data, our mission is simple: empower healthcare decisions regarding the safe and appropriate use of medicines for patients.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 assist 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 anticipate and troubleshoot roadblocks and influence teams to achieve targets for the division. Through your expertise and extensive knowledge, you will 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 degreeCompensation and Benefits The annual base salary for this position ranges from $99,900.00 to $166,500.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 15.0% of the base salary and eligibility to participate in our share-based long-term incentive program. We offer comprehensive and generous benefits to help our colleagues lead healthy lives and support each of life’s moments.Relocation assistance may be available based on business needs and/or eligibility.EEO & Employment Eligibility Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.About Us Pfizer careers are like no other. In our culture of individual ownership, we believe in our ability to improve future healthcare and potential to transform millions of lives. We’re looking for new talent to join our global community to unearth new innovative therapies that make the world a healthier place.
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Please make an application promptly if you are a good match for this role due to high levels of interest.Time Type: Full timePosted on: Posted YesterdayJob Requisition ID: 4917331Why Patients Need You Pfizer colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary expertise or investigating how to close gaps in data, our mission is simple: empower healthcare decisions regarding the safe and appropriate use of medicines for patients.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 assist 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 anticipate and troubleshoot roadblocks and influence teams to achieve targets for the division. Through your expertise and extensive knowledge, you will 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 degreeCompensation and Benefits The annual base salary for this position ranges from $99,900.00 to $166,500.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 15.0% of the base salary and eligibility to participate in our share-based long-term incentive program. We offer comprehensive and generous benefits to help our colleagues lead healthy lives and support each of life’s moments.Relocation assistance may be available based on business needs and/or eligibility.EEO & Employment Eligibility Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.About Us Pfizer careers are like no other. In our culture of individual ownership, we believe in our ability to improve future healthcare and potential to transform millions of lives. We’re looking for new talent to join our global community to unearth new innovative therapies that make the world a healthier place.
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