Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
Scoutfield Logo

See all jobs on Scoutfield

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Abbott

Clinical Site Lead

Abbott

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

Posted 11/4/2026full-timeRemote • United StatesSenior💰 $61,300 - $122,700 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in managing clinical trial processes, including site nomination, qualification, and monitoring, while ensuring compliance and protocol adherence. Possesses strong communication skills and the ability to collaborate effectively with clinical sites and commercial partners.

Highest-signal resume keywords
Clinical Trial ManagementSite Qualification and MonitoringData Collection and ComplianceClinical and Technical TrainingProblem-Solving and Decision-Making

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical Trial ExperienceProtocol AdherenceData Review and DocumentationOperational Metrics AnalysisCatheterization Lab Procedures
Soft Skills
Excellent Oral CommunicationExcellent Written CommunicationIndependent Problem-Solving
Certifications & Qualifications
Core Level Abbott Certification
Industry Keywords
Cardiovascular TherapiesClinical Trial SitesSite RecruitmentEnrollment ProcessesCompliance Standards

About the role

Key responsibilities & impact
  • Drive study execution and operational excellence across Abbott Cardiovascular therapies
  • Develop and maintain a productive clinical territory across the Indianapolis, Cincinnati, and Columbus territories
  • Identify, develop, qualify, and maintain clinical trial sites and investigators
  • Manage site nomination, qualification, startup, initiation, monitoring, and close-out processes
  • Lead ongoing training and retraining of site stakeholders on protocol adherence
  • Manage site recruitment, enrollment, data collection, discrepancy resolution, and compliance
  • Use operational metrics to minimize screen failure and attrition
  • Review site data and source documentation for accuracy and completeness
  • Facilitate resolution of data queries and clinical-site action items
  • Report monitoring findings and maintain complete monitoring records
  • Provide clinical and technical training and procedure coverage for clinical trials and commercial launches
  • Collaborate with commercial partners on product education and customer support
  • Maintain clinical and technical expertise and serve as a local resource

Requirements

What you’ll need
  • Bachelor's degree in engineering, science, health science, nursing, or a related field
  • 1 year 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)
  • Core level Abbott certification and/or equivalent level proficiency
  • Excellent oral and written communication skills
  • Independent problem-solving and decision-making ability
  • Current knowledge of clinical and Abbott product developments, competitive positioning, and published scientific and economic evidence

Benefits

Comp & perks
  • Career development with an international company
  • Free medical coverage eligibility through the Health Investment Plan (HIP) PPO medical plan
  • Retirement savings plan with high employer contribution
  • Tuition reimbursement
  • Freedom 2 Save student debt program
  • FreeU education benefit toward a bachelor’s degree
  • Employee diversity and workplace recognition programs