Remote Clinical Site Lead - Cardiovascular Trials

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

Benefits offered by this job

Free medical coverage

Strong retirement plan

Tuition reimbursement

FreeU degree program

Global employer recognition

Job summary

Abbott in the United States is seeking a Clinical Site Lead for Indianapolis, Cincinnati, and Columbus territories to drive study execution and operational excellence across cardiovascular therapies. You will lead site qualification, training, and data collection, ensuring regulatory compliance and timely enrollment.

This role requires a bachelor’s degree in a relevant field, 1 year of cardiovascular trial experience, and travel up to 50%.

Qualifications

• Bachelor’s degree in engineering, science, health science, nursing, or related field.
• 1 year of progressively more responsible relevant clinical trial experience in the cardiovascular field.
• Ability to travel approximately 50%.
• Preferred competency in catheterization lab and operating room protocol and procedures.

Responsibilities

• Develop and maintain a productive clinical territory: identify, develop, and maintain sites capable of delivering start-up goals, study participation levels and required data quality.
• Manage all aspects of study lifecycle to include site regulatory and quality: start up, nominate, approach, and complete qualification processes.
• Provide training and procedure coverage: apply clinical and technical expertise to train site and Abbott staff for clinical trials and applicable commercial launches.
• Collaborate with commercial partners: educate local sales groups on product launches and educate customers on Abbott products.

Education

Bachelor'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 for Indianapolis, Cincinnati, and Columbus territories to drive study execution and operational excellence across cardiovascular therapies. You will lead site qualification, training, and data collection, ensuring regulatory compliance and timely enrollment.

This role requires a bachelor’s degree in a relevant field, 1 year of cardiovascular trial experience, and travel up to 50%.