Regeneron Pharmaceuticals Associate Scientific Writer in Tarrytown, New York
Regeneron's Scientific Writing and Regulatory Liaisons group, located in Tarrytown NY, is seeking an Associate Scientific Writer to help provide support for the preparation of protein chemistry sciences documents, regulatory submission-supporting documents in the Preclinical Development and Protein Sciences group. In this role, you will independently draft and manage reviews of documents that focus on analytical chemistry and protein biochemistry across various therapeutic target areas.
A Typical Day in the Role of Associate Scientific Writer Might Look Like:
•Independently author protein chemistry sciences documents across various therapeutic target areas
•Provide editorial support, with a focus on clarity, accuracy, and consistency while maintaining adherence to proper format for manuscripts
•Adhere to a document process flow and alert appropriate personnel if a process change or delay occurs
•Initiate and manage multiple rounds of document review and ensuing revisions by proactively interacting with all levels of reviewers from subject matter expert to senior management
•Takes direction well and assumes responsibility for getting the work done
•Abide by GLP, GCP, and all company SOP's pertinent to the position
•Keeps current with software and regulatory guidances necessary for execution of job responsibilities
This Role Might Be For You If:
•You have strong attention to detail, establishing priorities and scheduling
•You are an excellent interpersonal and communication (verbal and written) skills
•You have a demonstrated ability to work effectively in a flexible environment
•You can work independently, take initiative and complete tasks to meet deadlines
This role requires a BS/MS degree in life sciences with 0-5 years meaningful experience. Basic background in the life sciences preferred. Must be proficient in preparing accurate, written reports. Computer proficiency (Word, Excel, Adobe and related software) and fluency in the English language is required.Basic understanding of the eCTD and the drug development process is a plus. GLP experience, as is previous experience with biotechnology-derived compounds is a plus.
Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides amazing benefits including health and wellness programs, fitness centers and stock for employees at all levels!
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or maternity status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. We will ensure that individuals with disabilities are provided reasonable accommodations to participate in the job application process. Please contact us to discuss any accommodations you think you may need.
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