Experienced Clinical Research Coordinator - Cardiology Preference

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Overview
We are seeking a highly motivated and experienced Clinical Research Coordinator with a strong preference for expertise in cardiology to join our dynamic research team. This role offers an exciting opportunity to lead and manage clinical trials focused on cardiovascular health, contributing to groundbreaking advancements in patient care. The ideal candidate will possess a deep understanding of clinical trial processes, excellent organizational skills, and a passion for improving health outcomes through research. As a vital member of our team, you will oversee study activities, ensure compliance with regulatory standards, and coordinate with multidisciplinary teams to facilitate successful trial execution.

Responsibilities

• Coordinate all aspects of clinical trials related to cardiology, including patient recruitment, enrollment, and follow-up
• Manage study documentation review, ensuring accuracy and completeness in accordance with FDA regulations and ICH GCP guidelines
• Monitor patient progress by collecting vital signs, blood samples, and conducting assessments while ensuring adherence to protocol procedures
• Oversee data collection and management using electronic medical record (EMR) systems and adhere to CDISC standards for data consistency
• Supervise clinical staff involved in trial activities, providing guidance on clinical procedures such as phlebotomy, blood sampling, and vital signs measurement
• Review laboratory results and clinical documentation to maintain high-quality data integrity and compliance standards
• Ensure adherence to HIPAA regulations and maintain patient confidentiality throughout all trial processes

Requirements

• Proven supervising experience in clinical research settings with a focus on cardiology or related fields
• Extensive knowledge of clinical trials management, including regulatory compliance under FDA regulations and ICH GCP certification from a recognized issuer for CA or other regions
• Strong understanding of medical terminology, clinical laboratory procedures, and patient monitoring techniques
• Experience with EMR systems, data management software, and statistical analysis tools such as SAS or SPSS
• Knowledge of clinical development phases, research methodologies, and compliance management practices
• Background in nursing or phlebotomy is highly desirable along with blood sampling expertise
• Excellent analysis skills with attention to detail for reviewing documentation and ensuring protocol adherence

Join us in advancing cardiovascular research by leveraging your expertise in clinical trials management! We are committed to fostering an inclusive environment that supports your professional growth while making meaningful contributions to healthcare innovation. All positions are paid roles dedicated to supporting your career development in the vital field of clinical research.

Pay: $25.00 - $35.00 per hour

Benefits:

• Dental insurance
• Health insurance
• Paid time off
• Vision insurance

Work Location: In person