Manager, Clinical Data Management, Study Lead

Regeneron

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Quick summary

Work type
On-site
Location
Tarrytown, NY
Salary
$172,994–$187,400 / yr
Employment
Full-time
Posted
20 days ago
Freshness
Confirmed live today
Closes
Oct 26, 2026

Market check

Salary context

Competitive pay

How this pay compares to similar roles

Similar $188k
This role $180k
$141k most similar roles pay here $234k

This role pays less than 55% of similar roles. Most pay $162,000–$214,900 — the shaded band above. At the midpoint, this role pays about $180k versus about $188k 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 57 open roles on FindRole.

Listed pay typically runs $134,400–$219,200 across 45 roles with salary data.

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View all roles at Regeneron

At a glance

TL;DR · Manager, Clinical Data Management, Study Lead

Manager, Clinical Data Management (CDM), Study Lead serves as the primary data management lead supporting clinical study teams and external partners on small or noncomplex studies or larger projects within a specific therapeutic area. The role involves coordinating all activities from study start-up to archiving, including eCRF and database design, data quality reviews, and managing data transfers with CROs. Responsibilities include reviewing study documentation like DMPs and validation specifications while maintaining eTMF records for inspection readiness. The position requires expertise in 21 CFR Part 11, ICH GCP Guidelines, and CDISC standards to manage the clinical data lifecycle. Candidates must be skilled in identifying root causes for complex issues, proposing risk mitigations, and collaborating with crossfunctional, geographically distributed teams. This role ensures all data management deliverables align with business needs within a regulated environment.

What you'll do

  • Coordinate all clinical data management activities from study start-up through archiving.
  • Provide expertise in data management to support eCRF and database design.
  • Perform data quality review procedures and coordinate data transfers with CROs.
  • Review and approve critical study documentation including DMPs, CRFs, and validation specifications.
  • Maintain eTMF documentation and perform quality reviews to ensure inspection readiness.
  • Monitor data quality, assess issue progress, and propose risk mitigation strategies.
  • Act as a Subject Matter Expert to provide training and represent data management in study forums.

What we're looking for

  • Bachelor's degree in Mathematics, Pharmaceutical Science, Pharmaceutics, or a related field.
  • 6 years of clinical data management experience in the biotechnology, pharmaceutical, or health-related industry.
  • Experience applying 21 CFR Part 11, ICH GCP Guidelines, and CDISC standards to clinical data activities.
  • Experience supporting and coordinating clinical studies within a regulated data processing environment.
  • Experience applying data management processes and best practices across the full clinical data lifecycle.
  • Experience evaluating data management workflows and recommending process improvements.
  • Experience resolving complex data issues by analyzing requirements and identifying root causes.
  • Experience preparing and delivering written documentation and verbal communications for crossfunctional teams.

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