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Manager, Clinical Data (On-Site)

8+ years
$97,300 – $194,700 annually
10 June 20, 2025
Job Description
Job Type: Remote Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Summary

Abbott is seeking an experienced Manager, Clinical Data to lead clinical data management activities within its Medical Devices division at the Maple Grove, Minnesota location. This pivotal, on-site role offers an exciting opportunity to oversee end-to-end data processes—from CRF design to database integrity—while mentoring a team of data professionals. You will collaborate closely with clinical operations and biostatistics teams to drive quality decision-making and regulatory submission readiness.


Key Responsibilities

  • Oversee the entire clinical data management process, including CRF design and edit check specifications.

  • Ensure delivery of clean, analysis-ready datasets through thorough data review and cleaning.

  • Lead, mentor, and develop a team of data specialists, promoting a culture of quality and accountability.

  • Develop and execute risk-based quality management systems, including risk assessments and data management plans.

  • Plan, organize, and execute tasks in alignment with regulatory standards and project timelines.

  • Monitor team performance to ensure adherence to SOPs, industry regulations, and internal standards.

  • Collaborate cross-functionally with clinical operations, biostatistics, and regulatory teams to support high-quality clinical trials.

  • Ensure readiness for regulatory submissions and contribute to audit and inspection preparedness.


Required Skills & Qualifications

  • Bachelor’s degree in a science-related field or equivalent experience.

  • Minimum 8 years’ experience in the pharmaceutical, biotechnology, or medical device industry.

  • Proven expertise in clinical data management and leadership roles.

  • Strong understanding of risk-based monitoring and quality management systems.

  • Exceptional organizational, planning, and analytical skills.

  • Excellent verbal and written communication abilities across organizational levels.

  • Ability to work in a fast-paced, cross-functional, and geographically diverse environment.


Perks & Benefits

  • Salary Range: $97,300 – $194,700 annually (may vary by location).

  • Free medical coverage under the HIP PPO plan.

  • Robust retirement savings plan with high employer contributions.

  • Tuition reimbursement and student debt relief through Freedom 2 Save.

  • Career advancement in a globally recognized, award-winning workplace.

  • Opportunity to lead innovation in medical device data management.


Company Description

Abbott is a global leader in healthcare innovation, providing life-changing technologies in diagnostics, medical devices, nutrition, and branded generics. Our mission is to improve lives worldwide by delivering reliable, effective healthcare solutions across the continuum of care.


Work Mode: On-site – Maple Grove, MN


Call to Action

Ready to drive innovation in clinical data management with a global healthcare leader? Apply today to become part of Abbott’s forward-thinking Clinical Affairs team and make an impact in medical device development.