Oncology Medical Writer (Senior Manager/Associate Director)
Pfizer - Long Island City, New York, United States, 11101![Pfizer](/api/image?src=https%3A%2F%2Fgeneral-board-default.s3.us-east-2.amazonaws.com%2Fpublic%2Fimages%2Fdesk-360x180.webp&w=640&q=75&f=webp)
Work at Pfizer
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Overview
The full job description covers all associated skills, previous experience, and any qualifications that applicants are expected to have.Locations: United States - New York - Remote, United States - Remote, Canada - Remote
Time Type: Full time
Posted on: Posted Yesterday
Job Requisition ID: 4917331
Why Patients Need YouPfizer colleagues play a key role in connecting evidence-based medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Our mission is simple: empower healthcare decisions regarding the safe and appropriate use of medicines for patients.
What You Will AchieveYour strong documentation skills will be an asset for the team. You will help 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.
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 collaboration 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 Degree
7+ years' experience
Medical writing experience in the pharmaceutical or biotech industry
Demonstrated ability to interpret and apply guidelines to document writing
Comprehensive understanding of the drug development process and regulatory knowledge
Excellent project management skills to organize work and handle multiple projects simultaneously
Ability to work independently with minimal supervision, multi-task, and work effectively under pressure
Experience with software commonly used to present and analyze data, such as Word, PowerPoint, Excel
Oncology writing experience strongly preferred
Nice-to-Have
Master's degree
The annual base salary for this position ranges from $99,900.00 to $166,500.00. 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 benefits to help our colleagues lead healthy lives, including a 401(k) plan with Pfizer Matching Contributions, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits.
Relocation assistance may be available based on business needs and/or eligibility.
About UsPfizer careers are like no other. In our culture of individual ownership, we believe in our ability to improve future healthcare and the 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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