Clinical Data Lead: CDM & Study Data Oversight

Sanofi

Morristown (NJ)

On-site

USD 110,000 - 140,000

Full time

2 days ago
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Benefits offered by this job

Parental leave 14 weeks
Health benefits
Global opportunities
Rewards package

Job summary

Sanofi US Services in Morristown, NJ seeks a Clinical Data Lead (Data Manager) to guide the data management strategy across clinical studies. You will ensure data integrity, oversee external vendors, and represent CDM within cross-functional teams to deliver clean databases for analysis and regulatory submission.

You will lead data management activities in line with standards and regulations, drive process improvements, and partner with Digital, Pharmacovigilance, and laboratories to advance

Qualifications

  • Bachelor's degree in health/Life Sciences or related field.
  • 3+ years of data management experience in clinical/medical fields.
  • Proficiency in data management software (Rave, EDC, eCOA), SAS and data visualization tools.
  • Solid understanding of clinical data standards and outsourcing oversight.

Responsibilities

  • Plan and coordinate data management activities per standards/regulations.
  • Oversee external vendors/partners as applicable.
  • Represent CDM with Clinical Team and other departments (Digital, Pharmacovigilance, Labs).
  • Ensure data quality and readiness for timelines, audit and inspections.
  • Contribute to improvement of global data management processes with business and project management skills.
  • Collaborate across Sanofi with various partners.

Skills

Rave
EDC systems
eCOA platforms
SAS
Data visualization
Project management
Outsourcing oversight

Education

Bachelor's degree in Life Sciences

Tools

Rave
EDC
eCOA

Job description

Sanofi US Services in Morristown, NJ seeks a Clinical Data Lead (Data Manager) to guide the data management strategy across clinical studies. You will ensure data integrity, oversee external vendors, and represent CDM within cross-functional teams to deliver clean databases for analysis and regulatory submission.

You will lead data management activities in line with standards and regulations, drive process improvements, and partner with Digital, Pharmacovigilance, and laboratories to advance

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