Regeneron

AssociateManager,ScientificWritingOperations

$110–179k Tarrytown, New York, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Manager candidates.

The Brief

“Associate Manager, Scientific Writing Operations at Regeneron. Skills: Project timelines, Resource management, Operational metrics. Manage project timelines and resources. Negotiate timelines across functional areas”

What You'll Achieve.

Ensure solutions are delivered on time; Ensure solutions are adopted by end users

Industry & Context.

Problems you'll solve

Root cause analysis

What They're Looking For.

Must Have

Bachelor's degree or MS/PhD/PharmD in life science, 3-5 years' experience in pharmaceutical industry, PPM (Project Portfolio Management Software) experience, Computer proficiency (Microsoft Office Suite, Adobe Acrobat), Basic experience with job-relevant AI usage

Nice to Have

Experience with operational/project management support for regulatory or technical writing deliverables, 1-2 years of experience participating in cross-functional drug development teams, Previous experience in supervising

What You'll Do.

Manage project timelines and resources

Negotiate timelines across functional areas

Assist with project sequencing

Manage creation and maintenance of document templates

and track implementation of technical solutions

Coordinate implementation activities

Track and report operational metrics

Recommend continuous improvement opportunities

Provide backup support for nonclinical document processes

Partner with cross-functional stakeholders

Define user requirements

Document business needs

Translate process gaps into technical enhancements

Create and review SOPs

Create and review Working Practices

Participate in drug development team meetings

Abide by GxP and regulatory guidelines

How You'll Work.

Team & Collaboration

Cross-functional stakeholders; Drug development teams

Process & Methodology

Project timelines, Resource planning, Project sequencing

Full Job Description

Assists in managing project timelines and resources and negotiates timelines across various functional areas. Assists with project sequencing, as directed by senior Scientific Writing Operations personnel. Tracks and reports operational metrics for Scientific Writing tools and processes (e.g., cycle times, throughput, adherence) and recommends continuous improvement opportunities. Manages creation and maintenance of document templates for cross-functional use. Supports, drives, and tracks implementation of technical solutions that enable Scientific Writing deliverables (e.g., authoring tools, templates, trackers, and workflow improvements). Coordinates implementation activities (testing/UAT, training materials, communications, and rollout plans) to ensure solutions are delivered on time and adopted by end users. **As an Assoc Manager, A typical day may include:** * Assists in managing project timelines and resources and negotiates timelines across various functional areas * Assists with project sequencing, as directed by senior Scientific Writing Operations personnel * Manages creation and maintenance of document templates for cross-functional use * Supports, drives, and tracks implementation of technical solutions that enable Scientific Writing deliverables (e.g., authoring tools, templates, trackers, and workflow improvements) and coordinates implementation activities (testing/UAT, training materials, communications, and rollout plans) to ensure solutions are delivered on time and adopted by end users * Tracks and reports operational metrics for Scientific Writing tools and processes (e.g., cycle times, throughput, adherence) and recommends continuous improvement opportunities * Provides backup support for nonclinical document processes to maintain continuity of key workflows (e.g., document routing, publishing/readiness checks, QC coordination, and handoffs between authors and reviewers) **You might be a good match for this role if you:** * Partners with cross-fu

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