Remote Clinical Site Lead – Cardiovascular Trials

Abbott; United States; Remote; USD 61,000 - 123,000; Full time

Benefits offered by this job

Free HIP PPO medical coverage

Excellent retirement plan

Tuition reimbursement

FreeU education benefit

Job summary

Abbott in the United States is seeking a Clinical Site Lead to join the field team covering Atlanta, GA and surrounding territory. You will drive study execution across cardiovascular therapies, oversee site qualification, startup, enrollment strategies, and data integrity while ensuring ICH-GCP compliance.

You will train site staff and Abbott colleagues, monitor performance, and escalate issues as needed. Travel up to 75% is required; a strong clinical research background is essential.

Qualifications

• Associates Degree required; 1 year experience in relevant field.
• Preferred: Bachelor’s Degree or Master’s Degree in engineering, science, health science, nursing, or a related field, OR equivalent or related experience in cardiology or clinical research.

Responsibilities

• Develop and maintain a productive clinical territory: identify and maintain sites capable of delivering start-up goals and data quality.
• Manage all aspects of study lifecycle including site regulatory and quality: start up, qualification, site initiation visits, and regulatory compliance.
• Enrollment: develop site-specific strategies to promote patient enrollment and monitor study performance and data.
• Regulatory and Quality: ensure GCP compliance, conduct data review, and escalate non-compliant sites as needed.
• Provide training and procedure coverage for clinical trials and commercial launches.

Skills

1 year experience

Education

Associates Degree

Bachelor’s Degree Or Master’s Degree in engineering, science, health science, nursing, or a related field

Job description

Abbott in the United States is seeking a Clinical Site Lead to join the field team covering Atlanta, GA and surrounding territory. You will drive study execution across cardiovascular therapies, oversee site qualification, startup, enrollment strategies, and data integrity while ensuring ICH-GCP compliance.

You will train site staff and Abbott colleagues, monitor performance, and escalate issues as needed. Travel up to 75% is required; a strong clinical research background is essential.