🧪 Job Title: Associate Clinical Site Lead
Category: Medical and Clinical Affairs
Location: United States – Minnesota – Minneapolis
Organization: Abbott Laboratories
🌍 About Abbott
Abbott is a global healthcare leader helping people live healthier and fuller lives.
Its innovative portfolio includes:
Diagnostics
Medical Devices
Nutritionals
Branded Generic Medicines
With 114,000+ employees across 160+ countries, Abbott is recognized globally as:
One of Fortune’s Most Admired Companies
A Top Employer for diversity, women, scientists, and working mothers
💼 Working at Abbott – Key Benefits
🌱 Career Growth: Global career development and training opportunities
🏥 Health Coverage: Free medical coverage under the Health Investment Plan (HIP) PPO
💰 Retirement Savings: High employer contribution
🎓 Education Support:
Tuition reimbursement
Freedom 2 Save student debt program
FreeU education benefit (bachelor’s degree pathway)
🌟 Recognition: Named among the Best Big Companies to Work For worldwide
🫀 Abbott Medical Devices Mission
Abbott’s medical device technologies improve patient lives across multiple therapeutic areas:
Glucose monitoring systems
Structural heart and cardiovascular therapies
Chronic pain and movement disorder management
💡 Every day, Abbott devices help 10,000+ people have healthier hearts and 500,000+ people manage diabetes without routine fingersticks.
🎯 Position Summary
Under supervision of a senior colleague/manager, the Associate Clinical Site Lead supports clinical study execution and drives operational excellence across Abbott’s cardiovascular therapies:
Vascular
Cardiac Rhythm Management (CRM)
Electrophysiology (EP)
Structural Heart
Heart Failure
The role focuses on developing core skills in:
Protocol execution
Product and disease knowledge
Clinical trial enrollment and compliance
ICH-GCP application
Site relationship management
⚙️ Key Responsibilities
1. Clinical Territory Development
Identify, develop, and maintain clinical sites capable of meeting study goals.
Assess investigators’ qualifications and align with study requirements.
Build strong relationships with site personnel (Principal Investigator, Research Coordinator, Regulatory Staff).
Facilitate communication between sites and internal Abbott teams.
Provide technical and clinical support as needed.
2. Study Lifecycle Management
🧩 Start-Up
Nominate and qualify clinical sites.
Conduct site initiation visits and establish expectations.
Ensure regulatory and legal compliance.
Train facility staff on protocol and device use.
👥 Enrollment
Develop site-specific patient recruitment strategies.
Monitor site performance, identify issues, and implement corrective actions.
Attend study procedures or ensure trained representatives attend.
✅ Regulatory & Quality
Maintain strong understanding of GCP and Abbott’s compliance standards.
Educate sites on compliance tools and strategies.
Escalate non-compliance per corporate policy.
Review source data, adverse events, and protocol deviations.
Resolve data queries and ensure accuracy of documentation.
Prepare detailed monitoring visit reports.
3. Training & Procedure Support
Train site and Abbott staff on trial protocols and new technologies.
Provide clinical expertise during trials and commercial product launches.
Attend or oversee study-related procedures and follow-ups.
4. Collaboration & Communication
Collaborate with commercial teams for new product launches.
Educate customers and sales teams on Abbott’s products.
Enhance customer experience through proactive communication.
Act as a resource for technical queries and troubleshooting.
5. Professional Development
Stay current on disease areas, Abbott technologies, and competitor products.
Maintain certifications and Abbott-required training.
Demonstrate independent problem-solving and strong communication skills.
🎓 Preferred Qualifications
Education:
Bachelor’s degree in Engineering, Science, Health Science, Nursing, or a related field
OR equivalent experience in Cardiology or Clinical Research
Experience:
Minimum 2 years of clinical trial experience (preferably in cardiovascular research)
Skills:
Competence in catheterization lab and operating room environments
Strong understanding of GCP, clinical procedures, and data management
Excellent communication, documentation, and problem-solving abilities
Willingness to travel up to 75%, including internationally
💰 Compensation
Base Pay Range:
💵 $50,000 – $100,000 (may vary by location)
🔗 How to Apply
👉 Visit: www.abbott.com
👉 Learn more about Abbott benefits: www.abbottbenefits.com
🤝 Equal Opportunity Statement
Abbott is an Equal Opportunity Employer, committed to diversity, inclusion, and a supportive work environment for all employees.
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