Associate Manager, Scientific Writing

Regeneron

. Coordinate authors of regulatory documents from a variety of disciplines within assigned projects .

Posted 9/30/2026full-timeRemote • United StatesJuniorMid-Level💰 $109,900 - $179,300 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in regulatory writing and project management within the pharmaceutical industry, with a strong focus on coordinating cross-functional teams and ensuring adherence to document processes. Proficient in identifying training needs and supporting professional development for team members.

Highest-signal resume keywords

Regulatory WritingProject ManagementCross-Functional Team CollaborationDocument Quality MonitoringTraining and Development

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Regulatory WritingProject ManagementDocument Quality MonitoringProcess ImprovementSOP Development

Soft Skills

Organizational SkillsInterpersonal SkillsCommunication Skills

Tools & Technologies

Microsoft Office SuiteAdobe AcrobatAI Tools

Industry Keywords

Pharmaceutical IndustryDrug DevelopmentRegulatory DocumentsDocument Processes

About the role

Key responsibilities & impact

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
Support assignment of deliverables and definition of project priorities under the direction of senior Scientific Writing team members
Coordinate regulatory document authors across disciplines, monitor document quality, and support staff training and professional development

Requirements

What you’ll need

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
Excellent organizational, interpersonal, and communication skills
Computer proficiency with Microsoft Office Suite, Adobe Acrobat, and related software
Basic experience with job-relevant AI usage
Fluency in English
Preferred: 1-2 years of experience participating in cross-functional drug development teams
Preferred: previous supervisory experience

Benefits

Comp & perks

annual bonuses or other incentive plans
equity awards
pension or retirement benefits
401(k) company match
health and wellness programs
fitness centers
medical, dental, vision, life and disability insurance benefits
paid time off
family support benefits
reasonable accommodation during the recruitment process where required