Medical Writer Job at Regeneron Pharmaceuticals in Armonk

Regeneron is seeking a Medical Writer who is highly motivated to learn the skills needed to write a variety of regulatory documents and publications to support Regeneron’s drug development programs. The position is within our Medical Writing group where the writer will receive hands-on writing clinical documents for regulatory submissions.

In this role, the Medical Writer will gain experience:

1. Drafting documents integral to clinical sites and regulatory submissions.
2. Drafting regulatory and technical documents to support the drug manufacturing process and controls.
3. Creating publications for submission to congresses and peer-reviewed journals to serve as citable references for the global scientific and medical community.
4. Leading the document life cycle, which includes content development, drafting, reviews, comment reconciliation, quality control, formatting, submissions, and storage in the appropriate document platform.
5. Developing and maintaining document timelines.
6. Interpreting data from nonclinical and clinical studies.
7. Working with representatives from multiple functions.
8. Working with mentors to improve skills to better reach professional goals.
9. Cross collaboration with Scientific Writing, Chemistry Manufacturing and Controls (CMC) Regulatory Sciences, and Publications groups may also occur with the goal of supporting further expertise in regulatory and publications writing in the pharmaceutical industry.

This role might be for you if:

1. Are highly motivated and seek to build a career with a foundation in Regulatory and Publications writing.
2. Can learn, interpret, and follow Regeneron policies and procedures, including SOPs and regulatory agency regulations.
3. Are willing to learn scientific, medical, pharmaceutical, and clinical research concepts.

To be considered for this opportunity, you must have:

1. Excellent attention to detail, ensuring accuracy and quality in the performance of all duties.
2. Strong planning, organization, and problem-solving skills (this includes excellent time management skills and ability to meet goals).
3. Strong written and oral (including interpersonal) communication skills, including detailed knowledge of the rules of grammar, sentence construction, and paragraphing in a scientific context.
4. Ability to work effectively in a team setting in a multicultural environment.
5. Ability to be flexible, multitask, work in a fast-paced environment, and adapt to changing priorities and goals.
6. A positive outlook.
7. Comfort in receiving objective feedback.

To be considered for this role you must have at minimum hold an MS and 3+ years of related experience with proven expertise in scientific writing (e.g., manuscripts, grants, or other scientific communications); or a Ph.D. with a minimum of 0-2 years’ experience as a strong preference.

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible 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 parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations.

Salary Range (annually): $108,300.00 - $176,700.00