Senior Medical Writer – Sr. Manager/Associate Director
Pfizer
full-time
Posted on:
Location Type: Remote
Location: Remote • 🇬🇧 United Kingdom
Visit company websiteJob Level
Senior
About the role
- 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 in Sub Business Unit/Sub Operating Unit.
Requirements
- 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
Benefits
- Flexible working hours
- Professional development opportunities
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
data analysisdocument writingproject managementprotocol authoringclinical document preparationstatistical analysis
Soft skills
analytical skillsproblem-solving skillswritten communicationverbal communicationcollaboration
Certifications
BABSMBAMSPhDJDMDDVM