Clinical Research Coordinator

Job Summary
We are seeking a dynamic and detail-oriented Clinical Research Coordinator to join our team and drive forward our innovative clinical trials. In this pivotal role, you will oversee the planning, execution, and management of clinical research studies, ensuring compliance with regulatory standards and maintaining the highest quality of data collection. Your expertise will help facilitate groundbreaking medical advancements while providing exceptional support to patients and research teams alike. This paid position offers an exciting opportunity to contribute to impactful healthcare research in a collaborative environment.

Responsibilities

• Coordinate and manage all aspects of clinical trials, including patient recruitment, enrollment, and retention.
• Review and verify study documentation for accuracy, completeness, and regulatory compliance.
• Monitor patient progress by conducting vital signs assessments, blood sampling, and other clinical procedures in accordance with study protocols.
• Ensure adherence to FDA regulations, ICH GCP guidelines, HIPAA privacy standards, and other applicable compliance requirements.
• Supervise research staff and collaborate with multidisciplinary teams to facilitate smooth trial operations.
• Manage data collection processes using EMR (Electronic Medical Record) systems and adhere to CDISC standards for data management.
• Conduct clinical laboratory procedures such as blood sampling and phlebotomy while maintaining safety protocols.
• Analyze study data using statistical software tools to support research findings and prepare reports for review.
• Oversee patient monitoring activities, including recording vital signs and adverse events during study visits.
• Review research documentation regularly to ensure accuracy, completeness, and regulatory compliance.
• Maintain detailed records of all trial activities, including consent forms, case report forms, and regulatory documents.

Requirements

• Proven supervising experience in clinical research or healthcare settings.
• Experience locating and identifying clinical studies that best fits the scope of our practice
• Strong knowledge of clinical trials management, including protocol development and regulatory submissions.
• Familiarity with medical terminology, clinical laboratory procedures, and blood sampling techniques.
• Experience with data collection, management systems (EMR), and statistical software used in research analysis.
• Understanding of FDA regulations, ICH GCP guidelines, HIPAA privacy rules, and CDISC standards for data interoperability.
• Clinical laboratory experience or nursing background preferred; certification such as ICH GCP certificate from a recognized issuer is highly desirable.
• Knowledge of clinical development processes across various phases of trials.
• Excellent documentation review skills with keen attention to detail.
• Ability to monitor patient vital signs accurately and perform phlebotomy safely when required.
• Strong organizational skills with the ability to manage multiple tasks efficiently while ensuring compliance standards are met. Join us in advancing healthcare through meticulous research coordination We are committed to fostering a supportive environment where your expertise makes a real difference in patient outcomes and medical innovation alike. This paid role offers valuable professional growth opportunities within a vibrant team dedicated to excellence in clinical research practices.

Job Type: Part-time

Pay: $ $25.00 per hour

Work Location: In person