How You Will Achieve It

• Contribute to the completion of complex projects, manage own time to meet agreed targets and develop plans for work activities on own projects within a team.
• Collaborate with clinical study team members to interpret study results and prepare Clinical Study Reports (CSRs) and related documents.
• Support teams by providing analyses of clinical data, post-marketing safety data, reviews of the medical literature, and similar related activities.
• Drive the document strategies and messages in a collaborative way with relevant project team subject matter experts.
• Independently plan and prepare medical writing deliverables, predominantly prose safety narratives, by organizing and interpreting safety and medical data.
• Assess document requirements, gauging their complexity and identifying information gaps.
• Performs at level-appropriate efficiency as assessed by speed, volume, complexity and quality metrics.

Qualifications

Must-Have

• Bachelor's Degree
• 3+ years’ experience
• Prior work experience in medical and scientific writing
• Ability to work well with all levels and roles in cross-functional, global teams
• Effective influencing and negotiating skills, including when appropriate an ability to guide decision-making for document content strategy
• Strong oral presentation skills, including ability to present, explain and defend data analyses before internal and external audiences
• Experience with software commonly used to present and analyze data (Word, PowerPoint, Excel)

Nice-to-Have

• Master's degree
• Relevant pharmaceutical industry experience

  
 

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

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