Instagram
youtube
Facebook

Associate Clinical Site Lead

2 years
$50,000.00 – $100,000.00
10 Sept. 9, 2025
Job Description
Job Type: Full Time Education: B.Sc/ M.Sc/ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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.