Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Associate Clinical Site Lead

Abbott
Abbott
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.