Associate Manager Scientific Writing
# Associate Manager Scientific Writing **Regeneron** · United States · `Remote` · `Full Time` 💼 **Уровень роли:** `Manager` 💰 **Компенсация:** `$109,900 – $179,300` 🕒 **Статус:** *Опубликовано: сегодня* · *Источник: Himalayas (JSON API)* --- ### Top Skills & Match 🎯 **Ключевой стек роли:** `[Scientific-Writer]` `[Regulatory-Writing]` `[Medical-Writer]` `[Associate-Manager]` `[Scientific-Writing-Manager]` `[Medical-Writing-Manager]` `[Scientific-Writing-Specialist]` --- ### About the Role Build our future together: At Regeneron , we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Team Lead to join our Scientific Writing group, supporting the assignment of deliverables and defining project priorities under the direction of senior SW team members. In this role, you will coordinate regulatory document authors across disciplines, monitor project timelines and document quality, and support training and professional development for staff, while participating as a member of cross-functional drug development teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. When & where: - Location: Remote - Work model/flexibility: Remote Discover your role: - Coordinate authors of regulatory documents from a variety of disciplines within assigned projects - Monitor project timelines and resources, escalating risks to management and supporting timeline negotiations across functional areas - Identify training and development needs of direct reports, providing support and guidance for personnel - Participate in screening and interviewing candidates to satisfy existing and new team needs - Support the creation and maintenance of document templates, SOPs, and working practices - Monitor adherence to document processes, escalating deviations to SW management - Identify areas for process improvement within assigned projects and communicate observations to management - Participate in relevant cross-functional drug development team meetings This role requires: - Bachelor's degree or MS/PhD/PharmD in a life science (advanced degree preferred) - 3-5 years of experience (BS/MS) or 2-3 years (PhD) in the pharmaceutical industry, including at least 3 years in regulatory writing - Ability to manage multiple projects with excellent organizational, interpersonal, and communication skills - Computer proficiency (Microsoft Office Suite, Adobe Acrobat, and related software), basic experience with job-relevant AI usage, and fluency in English - Preferred: 1-2 years of experience participating in cross-functional drug development teams - Preferred: previous supervisory experience Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit . For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. Please be advised that at Regeneron , we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location. As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications. For jobs in Canada: this posting is for an existing position. Salary Range (annually) $109,900.00 - $179,300.00 Originally posted on Himalayas
- Scientific-Writer
- Regulatory-Writing
- Medical-Writer
- Associate-Manager
- Scientific-Writing-Manager
- Medical-Writing-Manager
- Scientific-Writing-Specialist
Наблюдалась 2026-10-02, впервые 2026-10-02, источник — Himalayas (JSON API).