Logo for Regeneron

Associate Manager Scientific Writing

Role overview

Qualifications

  • Bachelor's degree or MS/PhD/PharmD in a life science
  • 3-5 years of experience in the pharmaceutical industry (BS/MS) or 2-3 years (PhD) in regulatory writing
  • Ability to manage multiple projects with excellent organizational, interpersonal, and communication skills
  • Computer proficiency (Microsoft Office Suite, Adobe Acrobat, and basic AI usage)

Responsibilities

  • Coordinate authors of regulatory documents from various disciplines within assigned projects
  • Monitor project timelines and resources, escalating risks to management
  • Identify training and development needs of direct reports and provide support
  • Participate in relevant cross-functional drug development team meetings

Key facts

  • Remote from: United States
  • Full time
  • Mid-level (2-5 years)
  • English

Hard skills

Other skills

  • Team Leadership
  • Organizational Skills
  • Social Skills
  • Verbal Communication Skills
  • Microsoft Office

About the company

Regeneron logo

Regeneron

Biotechnology

At Regeneron we believe that when the right idea finds the right team, powerful change is possible. As we work across our expanding global network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization. And new ways to think about health. Connect with us so we can learn more about you, and you can learn more about our biopharmaceutical medicines. And join us, as we build a future we believe in. Please visit www.regeneron.com/social-media-terms for information on how to engage with us on social media. An important note about privacy: Regeneron is committed to your privacy and will not ask for sensitive personal information such as social security number, date of birth or bank account details via email or social media.

Company details

Company typeLarge
IndustryBiotechnology
Company size10001

Your match analysis

See how your profile stacks up against this role.

We compared the job requirements to your profile to show where you're strong and where you fall short.

Job description

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

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. 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, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

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 https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. 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

Apply once. Then go straight to the hiring manager.

After you apply, unlock the direct contact details of the people who actually make the call. A quick follow-up makes you 5x more likely to land an interview.

MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
Unlocked after you apply
·

Related jobs

Other jobs at Regeneron

Premium

Reach out to the hiring manager directly.

Gain access to the contact details of the hiring managers who actually decide, and reach out to network with them directly. That, plus more when you upgrade:

  • Full match report with fit score and gaps
  • Career diagnostics on how recruiters read you
  • Curated company matches and warm intros
  • 48h early access to new roles

Cancel anytime.