Senior Clinical Site Lead

Abbott

. Drive study execution and operational excellence across Abbott Cardiovascular therapies .

Posted 11/4/2026full-timeRemote • United StatesSenior💰 $78,000 - $156,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial execution and operational excellence within cardiovascular therapies, ensuring compliance with ICH-GCP and regulatory standards while effectively managing site performance and stakeholder relationships.

Highest-signal resume keywords

Clinical Trial ManagementICH-GCP ComplianceSite Recruitment StrategiesData Collection PerformanceTechnical Support

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ExecutionProtocol AdherenceData AnalysisRegulatory ComplianceSite QualificationEnrollment StrategiesAdverse Event ReviewSource Documentation ReviewProblem SolvingDecision Making

Soft Skills

CommunicationTrainingCollaborationInfluencingRelationship Management

Industry Keywords

Cardiovascular TherapiesClinical ResearchGood Clinical PracticeCatheterization Lab ProtocolOperating Room Procedures

About the role

Key responsibilities & impact

Drive study execution and operational excellence across Abbott Cardiovascular therapies
Provide protocol execution, product and disease-state knowledge, procedure support, procedure outcome analysis, clinical trial enrollment, and ICH-GCP and clinical research application
Lead site nomination, qualification, startup, initiation, periodic, and close-out processes
Train and retrain site stakeholders to ensure protocol adherence
Manage and influence site recruitment and data collection performance
Use operational metrics to minimize screen failure and attrition
Monitor compliance with regulatory requirements, Good Clinical Practice, and accuracy standards
Identify, develop, and maintain clinical trial sites and investigators
Maintain relationships with principal investigators, research coordinators, regulatory personnel, and legal personnel
Provide technical support to customers and field staff
Facilitate communication between clinical sites and Abbott clinical staff
Develop site-specific enrollment and deviation-prevention strategies
Evaluate site performance and provide feedback
Attend study procedures and follow-ups or ensure trained personnel attend
Collect essential documents, obtain missing data, review adverse events and protocol deviations
Review source documentation and investigational-site data for accuracy and completeness
Resolve data queries and clinical-site action items
Report monitoring findings and maintain monitoring-visit records
Train site and Abbott staff for clinical trials and commercial launches
Provide clinical and technical procedure support as needed
Collaborate with commercial partners on product education and launches
Act as a technical resource for customer questions and troubleshooting
Maintain clinical and Abbott product expertise and serve as a local clinical and technical resource
Independently solve problems and make decisions

Requirements

What you’ll need

Bachelor's degree in engineering, science, health science, nursing, or a related field
2 years of progressively more responsible relevant clinical trial experience in the cardiovascular field
Ability to travel approximately 50%
Competency in catheterization lab and operating room protocol and procedures (preferred)

Benefits

Comp & perks

Career development with an international company
Free medical coverage eligibility through the Health Investment Plan (HIP) PPO medical plan in the next calendar year
Excellent retirement savings plan with high employer contribution
Tuition reimbursement
Freedom 2 Save student debt program
FreeU education benefit toward a bachelor’s degree
Health and wellness benefits
Equal Opportunity Employer committed to employee diversity