Associate Scientific Writer

Location
Tarrytown, NY, United States
Posted
Nov 11, 2020
Ref
20314BR
Required Education
Doctorate/PHD/MD
Position Type
Full time
The Scientific Writing and Regulatory Liaisons group is seeking an Associate Scientific Writer to help provide support for the preparation of nonclinical, regulatory submission-supporting documents and the associated submission summaries covering the functional areas of pharmacology, pharmacokinetics, toxicology and CMC (chemistry, manufacturing, and controls). We are looking for someone who can independently draft and manage reviews of documents for regulatory submission while focusing on nonclinical pharmacology across various therapeutic target areas. We are searching for a candidate to contribute to the drafting of related submissions and support documents as needed.

As the Associate Scientific Writer, a typical day might include the following:

- Collaborating closely with the scientific Subject Matter Expert (SME), initiating drafting and preparing the first draft of assigned documents
- Providing editorial support, ensuring quality of all scientific content, with a focus on clarity, accuracy, and consistency while maintaining adherence to proper format and regulatory requirements
- Initiating and managing multiple rounds of document review and ensuing revisions by proactively interacting with all levels of reviewers from SME to senior management
- Resolving conflicts and building consensus between all cross-functional groups and collaborators
- Directing multiple overlapping projects at different stages and on separate development programs and contributing to overall process improvement

This role may be for you if:

- You pay strong attention to detail while completing multiple projects and documents at once
- You have excellent communication and interpersonal skills, verbal and written
- You can work independently and take initiative to complete tasks in a deadline-oriented environment

To be considered for this opportunity, you must have a PhD degree in a life science. Additionally, 0-2 years of post-graduate experience in a non-research setting such as technical/medical/regulatory writing or program management is a plus. We need someone who is proficient in preparing accurate, written reports and is computer proficient with fluency in English. Please include a cover letter when submitting your application.

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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