Manager, Statistical Programming, Internal Medicine

Regeneron

Confirmed live today High trust

Hybrid

Quick summary

Work type: Hybrid
Location: Warren, NJCambridge, MATarrytown
Salary: $128,600–$210,000 / yr
Employment: Full-time
Posted: 2 days ago
Freshness: Confirmed live today
Nearby: 31 roles within 25 mi

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $190k

This role $169k

$117k $241k

below market most similar roles pay here above market

This role pays less than 68% of similar roles. Most pay $164,800–$214,900 — the blue band above. At the midpoint, this role pays about $169k versus about $190k for comparable roles.

Based on 240 similar postings.

Employer

About Regeneron

Regeneron is a leading science-driven biotechnology company that invents, develops, and commercializes life-transforming medicines for serious diseases.

Regeneron currently has 69 open roles on FindRole.

Listed pay typically runs $134,400–$241,200 across 55 roles with salary data.

Most-posted roles

View all roles at Regeneron

At a glance

TL;DR · Manager, Statistical Programming, Internal Medicine

Role Posting Log in to save

The Manager, Statistical Programming - Internal Medicine joins the Statistical Programming team to support a study team across the clinical portfolio. In this role, you will lead programming deliverables from a single study through regulatory approval, product launch, and annual reports. You will develop and quality control tables, listings, and graphs to support analysis requirements while managing programming efforts and complex ad hoc requests. You will serve as the programming representative on a multidisciplinary study team, collaborating with CROs and cross-functional colleagues. Key requirements include a Master's degree with 6+ years of experience or a BS with 7+ years of experience. You must demonstrate strong organizational and documentation skills within a regulated environment, providing input on hiring, feedback, and performance evaluations.

Skills

SAS Statistical Programming Tables Listings Graphs Quality Control Regulatory Approval Documentation

What you'll do

Lead programming deliverables from a single study through regulatory approval, product launch, and annual reports.
Develop and quality control tables, listings, and graphs to support specific analysis requirements.
Manage programming efforts by tracking progress and completing complex ad hoc requests.
Serve as the programming representative on a multidisciplinary study team to ensure timely support.
Partner with management to determine resource requirements for the therapeutic area or department.
Review resumes and screen candidates for contractor and permanent roles to support hiring.
Advise direct reports on procedures for data, records, and information retention.
Maintain rigorous quality and documentation standards within a regulated environment.

What we're looking for

Master's degree with 6+ years of relevant work experience.
BS degree with relevant work experience.
Proven experience leading programming deliverables within a clinical study team.
Experience providing input on hiring, feedback, and performance evaluation.
Strong organizational and documentation skills within a regulated environment.
SAS Certification (preferred).

Save