Senior Medical Writer (Sr. Manager/Associate Director)

Pfizer, S.A. de C.V; Remote; GBP 60,000 - 90,000; Full time

Job summary

A leading pharmaceutical company is seeking a Senior Medical Writer for a remote role. This position involves developing complex projects, collaborating with medical professionals, and interpreting scientific data. Ideal candidates should have a relevant degree and significant experience in medical writing, project management, and regulatory knowledge. Excellent communication skills are essential. Join us to make a meaningful impact on patient lives through innovative medical writing.

Qualifications

• 5+ years of experience in medical writing or related field.
• Strong experience in drug development process and regulatory knowledge.
• Ability to manage multiple projects simultaneously.

Responsibilities

• Develop and lead complex projects with comprehensive planning.
• Collaborate with clinicians and scientists to author protocols.
• Organize and interpret scientific data to prepare clinical documents.

Skills

Project management skills

Analytical and problem-solving skills

Exceptional written and verbal communication

Education

BA/BS or MBA/MS or PhD/JD or MD/DVM

Advanced degree in a relevant field

Tools

Microsoft Word

PowerPoint

Excel

Job description

Senior Medical Writer (Sr. Manager/Associate Director)

We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.

In this role you will:

• Develop and lead complex projects, creating comprehensive plans to meet objectives.
• Collaborate with clinicians, statisticians, and clinical scientists to author protocols and drive document strategies.
• Independently organize, analyze, and interpret scientific, clinical, and statistical data to prepare key clinical documents.
• Suggest improvements to document processes or templates to enhance quality and efficiency.
• Review the work of others within the assigned business unit.

Minimum Qualifications:

• BA/BS with strong experience or MBA/MS with 5+ years of experience or PhD/JD with some experience or MD/DVM with any years of relevant experience
• Demonstrated ability to interpret and apply guidelines to document writing, with a comprehensive understanding of the drug development process and regulatory knowledge
• Excellent project management skills to organize work and handle multiple projects simultaneously
• Experience with software commonly used to present and analyze data, such as Word, PowerPoint, and Excel
• Strong analytical and problem-solving skills
• Exceptional written and verbal communication skills

Preferred Qualifications:

• Advanced degree in a relevant field
• Experience in a leadership role within medical writing or a related field
• Familiarity with regulatory submission processes and requirements
• Ability to mentor and develop junior team members
• Strong interpersonal skills and the ability to work collaboratively with cross‑functional teams
• High level of attention to detail and organizational skills

Work Location: Remote – Field Based

Equal Employment Opportunity: All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, protected veteran status, or disability status.

We are a Disability‑Confident Employer and will make reasonable accommodations for qualified applicants with a disability.