Remote Regulatory Scientific Writer

Responsibilities:

• Researches, writes, and edits reports and data verification
• Summarizes data from clinical studies for submission to the relevant governing regulatory body
• Has experience in the analysis, summarization, and interpretation of scientific data and an ability to communicate early phase data succinctly, clearly, and accurately in writing

Qualifications:

• Minimum of a Bachelor’s degree is required
• Minimum 2+ years of industry experience is required
• Regulatory writing experience is required
• Data verification within Pfizer systems
• Enjoy working remotely while working with a Team
• Independent
• Ability navigate and maneuver through multiple systems
• Ability to change direction and come back to the task at hand
• Can work flexible hours (ability to attend meetings)

Please note contractors are engaged to provide services to Pfizer on a temporary basis in connection with a specific assignment. Contractors are hired and employed through Atrium, our third-party payrolling partner.