Remote Cardiology CRA – Monitor Trials & Data

Piper Companies; United States; Remote; USD 100,000 - 130,000; Full time

Benefits offered by this job

Health insurance

Vision insurance

Dental insurance

Paid time off (PTO)

Paid holidays

Sick leave

Job summary

Piper Companies is seeking a Cardiology Clinical Research Associate to monitor cardiovascular trials, ensure data integrity, and support site staff in compliance with ICH-GCP and FDA regulations.

Ideal candidates have a life sciences degree, 2+ years in clinical monitoring, experience with EDC/CTMS, and willingness to travel for site visits; the role offers a competitive salary and comprehensive benefits.

Qualifications

• Bachelor's degree in Life Sciences, Nursing, or related field.
• 2+ years of clinical research monitoring experience, preferably in cardiology trials.
• Strong knowledge of ICH-GCP guidelines and FDA regulations.
• Experience with EDC systems and clinical trial management tools.
• Excellent organizational, communication, and problem-solving skills.
• Ability to travel as required for site visits.

Responsibilities

• Monitor cardiology clinical trials at investigative sites to ensure adherence to protocols, GCP guidelines, and regulatory requirements.
• Conduct site initiation, routine monitoring, and close-out visits.
• Review source documents and CRFs for accuracy, completeness, and consistency.
• Identify, document, and resolve discrepancies in clinical data.
• Collaborate with investigators, study coordinators, and sponsors to ensure successful study execution.
• Maintain detailed documentation of site activities and monitoring reports.
• Ensure all adverse events and safety data are reported appropriately.

Skills

GCP compliance

Regulatory knowledge

Organization

Communication

Problem-solving

Travel readiness

Education

Bachelor's degree in Life Sciences or Nursing

Tools

EDC systems

Clinical trial management tools

Job description

Piper Companies is seeking a Cardiology Clinical Research Associate to monitor cardiovascular trials, ensure data integrity, and support site staff in compliance with ICH-GCP and FDA regulations.

Ideal candidates have a life sciences degree, 2+ years in clinical monitoring, experience with EDC/CTMS, and willingness to travel for site visits; the role offers a competitive salary and comprehensive benefits.