Senior Medical Writer
1 week ago
About the Role:
We are seeking a highly skilled Senior Medical Writer to join our team. As a Senior Medical Writer, you will be responsible for creating high-quality clinical study documents, including protocols, clinical study reports, and regulatory submissions.
Key Responsibilities:
- Develop complex clinical study documents that meet regulatory requirements and internal standards
- Lead project teams through the document development process and collaborate with subject matter experts and quality assurance professionals
- Manage project timelines and deliver assigned documents on or before deadlines
- Communicate effectively with cross-functional teams and stakeholders to ensure clear and concise presentation of analyses and associated discussions
Requirements:
- Bachelor's degree in a life science discipline, or equivalent experience
- At least 7 years of experience in medical writing or related field, with a strong understanding of regulatory requirements and corporate policies
- Excellent communication and interpersonal skills, with ability to work effectively in a global team environment
- Proficiency in Microsoft Office, particularly Word, Excel, and PowerPoint
Preferred Qualifications:
- Advanced degree (MS/MA/PhD) in a relevant field
- Prior experience with document management systems and collaboration software
Compensation and Benefits:
The annual base salary for this position is $99,900 - $166,500, depending on location. This role is eligible for participation in Pfizer's Global Performance Plan, with a bonus target of 15% of the base salary. Additionally, this position offers comprehensive benefits, including health insurance, retirement savings plan, paid time off, and more.
About Lifelancer:
Lifelancer is a talent-hiring platform connecting professionals with opportunities in life sciences, pharma, and IT. We pride ourselves on providing a collaborative and supportive work environment that fosters growth and innovation.
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