Senior Manager, Clinical Publications Writer

The Senior Manager/Clinical Scientific Publication Writing will assist authors with writing and development of our publications on scientific, clinical, health outcomes or other research. These will include our journal manuscripts, scientific conference abstracts, presentations, and digital enhancements. You are expected to initiate and drive publication projects in collaboration with publication teams and partners. 

You will work under authors’ guidance to develop scientific narratives aligning with our publication strategy, interpret scientific data and statistical analyses to ensure accuracy and readability, and manage timelines to achieve timely publication. 

This can be a remote position in the US only with occasional travel to Sleepy Hollow, NY. 

A typical day may include the following: 
•    Providing medical writing expertise for our products/therapeutic areas to achieve communication of accurate, objective, and balanced information in our publications.
•    Collaborating with a publication manager, vendor, and collaborators, with mentorship support from internal writers.
•    Learning and acquiring our therapeutic area and product knowledge applying to publication projects, including literature searches.
•    Developing a firm understanding of clinical study design, statistics, and pharmaceutical research & development.
•    Writing and editing the content of scientific, clinical, or health-outcomes abstracts, posters, presentations, digital enhancements, and manuscripts aligned with scientific narrative and objectives. Incorporating author/reviewer feedback and achieving comment resolution.
•    Completing publication reviews, quality checks, approvals, submissions, copy editing, page proof review, and production, in collaboration with our publication lead(s)/vendor agency
•    Assuming responsibility for accurate documentation, working with all collaborators, including senior scientists and internal/external authors, in all phases of publication development.

This may be for you if you: 
•    Want to be part of a growing oncology/hematology program
•    Have experience working on publications for multiple therapeutic areas
•    Have driven projects to successful completion
•    Have experience writing manuscripts, abstracts, and posters, under the guidance of authors
•    Have strong project management skills and can attain results with senior leaders
•    Understand GPP, ICMJE, and other publication/scientific communication guidelines
•    Proficiency in medical journal/medical writing search engines

To be considered, you must have a Master’s degree in a life science (a PhD, PharmD or MD preferred). Your experience should include over 3 years scientific and clinical writing of journal articles from a biopharma and/or medical communications agency. 

A strong scientific background, with the ability to understand complex research data and clinical trial results and health-outcomes research, clinical study design and statistics, is required. Your experience will include writing and critical review of abstracts, presentations, and manuscripts. High-level understanding of good publications practices (e.g., ICMJE, GPP, CONSORT, and US Sunshine Act) and relevant journal and congress guidelines. Experience with oncology or hematology is preferred. 
 

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. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.

For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions.  For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.

Please note that certain background checks will form part of the recruitment process.  Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.

Salary Range (annually)