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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing clinical trial operations, including site regulatory compliance, enrollment strategies, and performance evaluation. Possesses strong knowledge of ICH-GCP and clinical research protocols, along with effective communication and problem-solving skills.
Highest-signal resume keywords
Clinical Trial ManagementICH-GCP KnowledgeSite Regulatory ComplianceCatheterization Lab ProtocolsCore Level Abbott Certification
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Trial ExecutionData CollectionMonitoring ActivitiesEnrollment StrategiesRegulatory RequirementsQuality AssuranceTechnical Procedure SupportOperational Metrics EvaluationProtocol TrainingSite Performance Evaluation
Soft Skills
Excellent Communication SkillsIndependent Problem-SolvingDecision-Making Ability
Certifications & Qualifications
Core Level Abbott Certification
Industry Keywords
Cardiovascular TherapiesClinical ResearchGood Clinical PracticeClinical Trial SitesClinical Trial Investigators
About the role
Key responsibilities & impact- Drive study execution and operational excellence across Abbott Cardiovascular therapies
- Develop and maintain a productive clinical territory for the Cleveland, OH and Buffalo, NY surrounding territory
- Identify, develop, qualify, and maintain clinical trial sites and investigators
- Manage site regulatory, quality, startup, initiation, enrollment, monitoring, and close-out activities
- Train and retrain site stakeholders on protocol requirements, technology, compliance, and clinical trials
- Develop site-specific enrollment and deviation-prevention strategies
- Evaluate site performance, recruitment, data collection, compliance, and operational metrics
- Attend study procedures and follow-ups or ensure trained personnel attend
- Collect essential documents, resolve missing data and data queries, and review source documentation
- Report monitoring findings and maintain complete monitoring records
- Provide clinical and technical procedure support
- Collaborate with commercial partners on product launches, customer education, technical questions, and troubleshooting
- Maintain clinical, technical, product, competitive, scientific, and economic knowledge
- Act as a local clinical and technical resource
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
- Core level Abbott certification and/or equivalent level proficiency
- Knowledge of ICH-GCP, clinical research application, applicable regulatory requirements, and Good Clinical Practice
- Excellent oral and written communication skills
- Independent problem-solving skills and ability to make decisions
Benefits
Comp & perks- Career development with an international company
- Free medical coverage qualification 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 wellness and health benefits
- Equal Opportunity Employer committed to employee diversity