Manager Medical Writing

Pfizer; Województwo mazowieckie; Hybrid; PLN 120,000 - 160,000; Full time

Job summary

A leading global biopharmaceutical company in Poland is seeking an experienced professional to lead projects requiring medical writing and document quality control. The ideal candidate should have a background in document QC with a minimum of 4 years of experience and proficiency in Microsoft Office. This role offers a hybrid work environment and emphasizes flexibility and teamwork. Join us in transforming patients' lives through innovation and excellence.

Qualifications

• At least 4 years of experience in document QC or medical writing.
• Experience interacting with cross-functional teams.
• Solid understanding of medical terminology and clinical trials.

Responsibilities

• Lead or co-lead moderately complex projects.
• Review work and mentor colleagues.
• Verify document accuracy and perform Quality Control reviews.

Skills

Project management

Medical writing

Interpersonal communication

Problem-solving skills

Ability to prioritize tasks

Proficiency in Microsoft Office

Education

BA/BS or equivalent experience

Master's degree

Tools

Microsoft Office

Job description

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

• 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, 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

Purpose

Breakthroughs that change patients' lives... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.

Digital Transformation Strategy

One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.

Flexibility

We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let’s start the conversation!

Equal Employment Opportunity

We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.

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 [e-mail].