Manager, Clinical Data Review: Lead Data Integrity & Trials

Abbott

Los Angeles (CA)

On-site

USD 114,000 - 228,000

Full time

14 days+
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Benefits offered by this job

Health insurance
Retirement plan
Tuition reimbursement
FreeU education benefit
Career development

Job summary

Abbott in Sylmar, CA seeks a Manager, Clinical Data Review to lead our data management team on-site. You will oversee data entry, CRF design, data cleaning, and analysis-ready datasets, ensuring database integrity and regulatory compliance.

You’ll mentor staff, manage subcontractors, and align goals with quality systems and company values. This role requires a science degree, 8+ years in pharma/biotech/medical devices, and strong leadership, communication, and technical skills with Oracle

Qualifications

  • Bachelor's degree in a science-related field or equivalent experience.
  • 8+ years’ progressively responsible experience in pharma, biotech or medical device industry.
  • Advanced computer skills in graphics, word-processing, databases, and related tools.

Responsibilities

  • Hire and develop a diverse, qualified data management staff and provide coaching and performance feedback.
  • Oversee data entry, data cleaning, and data deliverables.
  • Develop CRFs, edit checks, and data collection requirements for tracking and analysis.
  • Ensure data integrity and regulatory compliance across processes.
  • Provide outputs from clinical databases to other departments as needed.
  • Stay current on industry regulations and train staff accordingly.
  • Support Quality Management Systems and regulatory requirements.

Skills

Staff leadership
Data integrity
Regulatory compliance
Communication
Team mentoring

Education

Bachelor's degree in science

Tools

Oracle Clinical

Job description

Abbott in Sylmar, CA seeks a Manager, Clinical Data Review to lead our data management team on-site. You will oversee data entry, CRF design, data cleaning, and analysis-ready datasets, ensuring database integrity and regulatory compliance.

You’ll mentor staff, manage subcontractors, and align goals with quality systems and company values. This role requires a science degree, 8+ years in pharma/biotech/medical devices, and strong leadership, communication, and technical skills with Oracle

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