Research Coordinator

Clinical Research Coordinator

Coastal Health

Coastal Health is seeking an experienced and motivated Clinical Research Coordinator (CRC) to join our research team. The ideal candidate will have a strong background in clinical research, excellent organizational skills, and the ability to coordinate research activities while ensuring compliance with study protocols and regulatory requirements.

Minimum Qualifications

• Bachelor’s degree in a health-science-related field required.
• Minimum of 2 years of experience working as a Clinical Research Coordinator required.
• Experience coordinating clinical research studies from start-up through completion.
• Strong understanding of clinical research protocols, regulatory requirements, and documentation.
• Excellent organizational, communication, and interpersonal skills.
• Ability to manage multiple priorities and meet study deadlines.
• Strong attention to detail and commitment to maintaining accurate research records.
• Ability to work effectively with investigators, research staff, study participants, sponsors, and other healthcare professionals.
• Ability to perform the essential physical and job-related requirements of the position.
  
  

Key Responsibilities

• Coordinate and manage day-to-day activities for assigned clinical research studies.
• Ensure study activities are conducted according to protocols, regulatory requirements, and company policies.
• Assist with participant recruitment, screening, enrollment, and follow-up.
• Maintain accurate and complete study documentation and regulatory files.
• Coordinate study visits, procedures, and communication with participants and clinical staff.
• Collect, document, and maintain study data.
• Communicate with study sponsors, monitors, investigators, and other research personnel as needed.
• Assist with regulatory submissions and maintain compliance documentation.
• Prepare for and assist with monitoring visits, audits, and inspections.
• Protect participant confidentiality and ensure adherence to applicable privacy and research regulations.
• Perform other duties related to the successful coordination of clinical research studies.
  
  

Preferred Qualifications

• Experience working in a clinical research, healthcare, or academic research setting.
• Familiarity with electronic data capture (EDC) systems and clinical research databases.
• Knowledge of Good Clinical Practice (GCP) guidelines.
• Experience working with multiple clinical trials or research protocols.
  
  

Application Requirements

Applicants must meet both of the following requirements to be considered:

• Bachelor’s degree in a health-science-related field.
• At least 2 years of Clinical Research Coordinator experience.
  
  

Qualified candidates should submit a current CV/resume for consideration.

Qualifications

• Bachelors degree in health, science or research-related field
• Two years experience in research or healthcare environment
• Detail-oriented individual with the ability to collect, document and analyze information
• Demonstrate professional communication (written and verbal)
• Demonstrate ability to establish rapport and maintain professional interaction skills
• Ability to communicate research protocol requirements effectively to potential trial participants and team members
• Ability to work independently, manage time effectively, prioritize tasks and work efficiently