Associate Clinical Site Lead
Location: [Insert Location]
Business Unit: Abbott Cardiovascular
Pay Range: $50,000 – $100,000 (location dependent)
About Abbott
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio spans diagnostics, medical devices, nutritionals, and branded generic medicines. With 114,000 colleagues across 160+ countries, we are recognized as one of the most admired companies in the world and a top workplace for diversity, working mothers, female executives, and scientists.
Why Work at Abbott
At Abbott, you can do work that matters, grow and learn, and live a full life with:
Career development opportunities in a global company.
Free medical coverage (Health Investment Plan PPO) in the next calendar year.
Excellent retirement savings plan with high employer contributions.
Tuition reimbursement, Freedom 2 Save student debt program, and FreeU bachelor’s degree program.
Recognition as one of the best big companies to work for worldwide.
Role Summary
Under the supervision of a senior colleague/manager, the Associate Clinical Site Lead supports study execution and operational excellence across Abbott Cardiovascular therapies (Vascular, Cardiac Rhythm Management, EP, Structural Heart, Heart Failure).
The role involves:
Driving clinical trial execution.
Supporting protocol adherence and training.
Monitoring site performance, compliance, and data accuracy.
Contributing to clinical trial enrollment and patient outcomes.
Developing expertise in cardiovascular clinical research.
Key Responsibilities
Clinical Territory Development
Identify, develop, and maintain qualified clinical sites.
Assess investigator interests and qualifications per study requirements.
Build and maintain strong relationships with Principal Investigators, Research Coordinators, and site staff.
Facilitate communication between sites and Abbott teams.
Provide ongoing technical support to customers and field staff.
Study Lifecycle Management
Start-Up:
Lead site nomination, qualification, and initiation processes.
Train facility staff on protocol requirements and Abbott technologies.
Enrollment:
Develop site-specific patient enrollment strategies.
Monitor performance, identify challenges, and recommend solutions.
Provide feedback and support to sites.
Regulatory & Quality:
Ensure compliance with GCP, ICH, and Abbott policies.
Collect, review, and resolve essential documentation, data discrepancies, adverse events, and deviations.
Conduct monitoring visits and provide reports per Abbott processes.
Training & Procedure Coverage
Deliver clinical/technical training to site and Abbott staff.
Provide procedure support during trials and product launches.
Collaboration & Communication
Partner with commercial teams for product education and customer engagement.
Act as a technical resource for Abbott products and clinical practices.
Stay current with scientific, clinical, and competitive developments.
Qualifications
Required
Bachelor’s degree in engineering, science, health science, nursing, or related field; or equivalent experience in cardiology/clinical research.
Minimum 2 years of progressively responsible clinical trial experience in cardiovascular field.
Competency in catheterization lab and operating room procedures.
Willingness to travel up to 75% (domestic & international).
Preferred
Strong understanding of GCP, clinical trial regulations, and site compliance.
Excellent oral and written communication skills.
Independent problem-solving and decision-making ability.
Certification(s) relevant to cardiovascular field (preferred, not mandatory).
✅ This format makes the job posting clear, scannable, and professional.
Andra Pradesh :
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