Manager Medical Writing

Use Your Power for Purpose

By connecting evidence-based medical decision support with colleagues and stakeholders, you will help achieve better health and treatment outcomes. Your work will ensure our evidence is scientifically robust, provide unbiased and medically necessary expertise, and investigate ways to close data gaps. Your role is crucial in enabling the safe and appropriate use of medicines for patients, ultimately contributing to our mission of empowering healthcare decisions.

What You Will Achieve

In this role, you will:

• Lead or co-lead moderately complex projects, effectively managing time and resources.
• Apply skills and knowledge to contribute to departmental work.
• Make decisions to resolve moderately complex problems and operate independently in ambiguous situations, guided by policies.
• Work independently on assignments, receiving guidance on unusual or complex problems.
• Review your own work, seek feedback from others, and mentor colleagues by reviewing their work.
• Utilize judgment and experience to potentially become a resource for others.
• Collaborate with project team experts to develop document strategies and messages.
• Ensure documents meet internal standards, are submission-ready, and properly stored.
• Verify document accuracy using source materials, including clinical regulatory documents and data.
• Lead teams of authors for complex projects, perform Quality Control reviews, and contribute to colleague training on quality standards and processes.

Here Is What You Need (Minimum Requirements)

• BA/BS with at least 4 years of experience or MBA/MS with at least 2 years of experience or PhD/JD with any years of experience or associate's degree with at least 8 years of experience or high School Diploma (or Equivalent) with at least 10 years of relevant experience
• Demonstrated experience in document QC and/or medical writing in the pharmaceutical or biotech industry
• Experience in interacting with cross-functional study team members
• Solid understanding of medical terminology and clinical trials
• Excellent interpersonal and communication skills
• Ability to plan, organize, prioritize, and execute multiple tasks within assigned objectives
• Proficiency with Microsoft Office applications

Bonus Points If You Have (Preferred Requirements):

• Master's degree is highly desirable
• Proficiency in software commonly utilized for data presentation and analysis
• Strong problem-solving skills and the ability to operate independently in ambiguous situations
• Experience in leading or co-leading projects
• Experience in training colleagues on quality standards and processes

Work Location Assignment: Hybrid

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.

Medical