Remote Associate Clinical Site Lead – Cardio Trials

Thornton Tomasetti; United States; Remote; USD 51,000 - 101,000; Full time

Benefits offered by this job

Career development with international

Free medical coverage in HIP PPO plan

Tuition reimbursement and education

Excellent retirement savings plan with

Job summary

Abbott is seeking an Associate Clinical Site Lead for the Atlanta, GA region to drive study execution and operational excellence across cardiovascular therapies. You’ll build protocol execution skills, gain disease state knowledge, and support sites through enrollment and data quality.

This role emphasizes GCP compliance, regulatory knowledge, and collaboration with site staff and Abbott teams to ensure high-quality trial outcomes.

Qualifications

• Required Associate’s degree with at least 1 year of experience.
• Preferred Bachelor’s Degree in engineering, science, health science, nursing, or related field, or equivalent experience in cardiology or clinical research.
• 2 years of progressively more responsible clinical trial experience in the cardiovascular field.
• Competency in catheterization lab and operating room protocol and procedures.
• Independent problem-solving skills and ability to make decisions.
• Excellent oral and written communication skills.

Responsibilities

• Develop and maintain productive clinical territory with start-up goals and data quality.
• Identify investigators and assess qualifications.
• Maintain open communication with site personnel and regulatory staff.
• Provide ongoing technical support to customers and field staff.
• Coordinate site start-up, initiation visits, and regulatory compliance.
• Collaborate with clinical and commercial teams on launches.

Skills

Communication skills

Clinical trial experience

Problem solving

Education

Associate’s degree

Bachelor’s degree or related field

Job description

Abbott is seeking an Associate Clinical Site Lead for the Atlanta, GA region to drive study execution and operational excellence across cardiovascular therapies. You’ll build protocol execution skills, gain disease state knowledge, and support sites through enrollment and data quality.

This role emphasizes GCP compliance, regulatory knowledge, and collaboration with site staff and Abbott teams to ensure high-quality trial outcomes.