
Associate Director Medical Writing
Pfizer is seeking a highly motivated and experienced Associate Director of Medical Writing to join our dynamic team. As a global leader in the pharmaceutical industry, Pfizer is dedicated to improving the lives of patients through the development and delivery of innovative medicines. In this role, you will have the opportunity to make a significant impact on the medical writing strategy and execution for our clinical trials and regulatory submissions. We are looking for an individual with a strong background in medical writing and a passion for delivering high-quality documents that meet regulatory and scientific standards. If you are a detail-oriented, team player with excellent communication and leadership skills, we encourage you to apply for this exciting opportunity at Pfizer.
- Develop and implement medical writing strategies for clinical trials and regulatory submissions in accordance with Pfizer's standards and guidelines.
- Manage and oversee the production of high-quality medical writing documents, including clinical study protocols, clinical study reports, investigator brochures, and regulatory submissions.
- Collaborate with cross-functional teams to ensure timely delivery of medical writing documents that meet regulatory and scientific standards.
- Review and edit documents for accuracy, consistency, and clarity, ensuring adherence to Pfizer's style and format guidelines.
- Provide guidance and mentorship to junior medical writers to ensure their professional growth and development.
- Stay updated on industry trends and best practices in medical writing to continuously improve processes and document quality.
- Act as the primary point of contact for medical writing-related queries from internal and external stakeholders.
- Coordinate and manage timelines for medical writing deliverables and ensure they are met.
- Ensure compliance with all relevant regulations, guidelines, and standard operating procedures.
- Contribute to the development and maintenance of medical writing templates, processes, and procedures.
- Act as a representative of Pfizer in interactions with regulatory authorities and external partners.
- Maintain a high level of confidentiality and adhere to ethical standards in all medical writing activities.
- Collaborate with cross-functional teams to resolve any issues or challenges related to medical writing.
- Participate in the training and development of colleagues and team members.
- Act as a role model for Pfizer's values and culture, promoting a positive and inclusive work environment.
Advanced Degree In A Relevant Scientific Field, Such As Pharmacology Or Medicine.
Minimum Of 5 Years Experience In Medical Writing In The Pharmaceutical Industry, With A Focus On Regulatory Documents.
In-Depth Knowledge Of Fda And Ich Guidelines For Document Preparation And Submission.
Strong Understanding Of Clinical Development Processes And Experience Working On Multiple Phases Of Clinical Trials.
Proven Leadership Skills And Ability To Effectively Manage A Team Of Medical Writers.
Project Management
Data Analysis
Time Management
Clinical Research
Leadership
Team Building
Drug development
Scientific writing
Regulatory compliance
Cross-Functional Collaboration
Publication Planning
Medical Communication
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Time management
creativity
Attention to detail
Teamwork
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Associate Director Medical Writing in Collegeville, PA 19426, USA is $140,000 - $200,000 per year. This may vary depending on the specific job responsibilities, experience level, and company.
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Pfizer Inc. is an American multinational pharmaceutical corporation headquartered in New York City, with its research headquarters in Groton, Connecticut. It is one of the world's largest pharmaceutical companies.

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