Epidemiology Study Operations Manager

AbbVie

. Strategically manage and oversee epidemiology-led non-interventional studies with progressive autonomy .

Posted 10/6/2026full-timeRemote • Illinois • United StatesMid-LevelSenior💰 $109,500 - $208,500 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing epidemiology-led non-interventional studies, including project management, vendor oversight, and regulatory compliance. Proficient in coordinating study deliverables and collaborating across functions to drive successful outcomes.

Highest-signal resume keywords

Project ManagementEpidemiology-Led StudiesVendor ManagementRegulatory ComplianceDrug Development

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Project Management ActivitiesRisk ManagementNon-Interventional Study Lifecycle ManagementPharmacovigilanceMedical TerminologyStudy Protocol DevelopmentDocument Quality ManagementAction Completion TrackingBudget OversightAudit Preparation

Soft Skills

CollaborationRelationship BuildingProblem SolvingAdaptability

Tools & Technologies

Clinical Trial Management SystemsWindowsWordExcel

Industry Keywords

HealthcarePharmaceutical IndustryResearch InstitutionGlobal Companies

About the role

Key responsibilities & impact

Strategically manage and oversee epidemiology-led non-interventional studies with progressive autonomy
Support the Study Leader with vendor selection, scope development, management, and oversight of external vendors/CROs
Manage and coordinate study-related deliverables, including project plans, timelines, accountabilities, document quality, action completion, and risk escalation
Drive study deliverables to meet regulatory and process timelines
Provide study-status updates to cross-functional teams and stakeholders
Use applicable systems and processes to track and complete studies and related deliverables
Coordinate development, review, and approval of study protocols and related documents
Maintain study documents, including meeting minutes and IRB/EC approvals, in the appropriate repository
Oversee funds spent against the approved budget
Identify, address, and escalate project-related issues
Identify efficiency opportunities and participate in department projects
Apply regulations knowledge to guide development of study deliverables
Collaborate across functions and organizations to achieve business results
Participate in audit and inspection preparation and execution

Requirements

What you’ll need

Bachelor’s degree in biological/medical science or healthcare professional
6+ years of experience working in healthcare, a research institution, or the pharmaceutical industry
Minimum 2 years driving project management activities or operational experience within global companies
Preferred experience in drug development, non-interventional study lifecycle management, risk management, and/or pharmacovigilance
Ability to work and collaborate with others to build and leverage relationships
Ability to adopt process and technology changes
Familiarity with medical and study terminology and concepts is desirable
Proficiency in Windows, Word, and Excel
Proficiency in databases, such as clinical trial management systems

Benefits

Comp & perks

Paid time off (vacation, holidays, sick)
Medical, dental, and vision insurance
401(k)
Long-term incentive program eligibility