Clinical Research Coordinator

DCND is looking to hire a Clinical Research Coordinator to add to our Research team. A Clinical Research Coordinator (CRC) is responsible for managing and coordinating the day-to-day operations of assigned clinical trials, ensuring they are conducted ethically and in accordance with regulations and protocols. Their duties encompass participant recruitment, data collection, regulatory compliance, and communication with various stakeholders. This person will work under the direction of the Research Manager and Primary Coordinator.

• Participant Recruitment and Management:
  Identifying, screening, and enrolling eligible participants, obtaining informed consent, and managing participant data.
• Data Collection and Management:
  Collecting, processing, and managing clinical data, ensuring accuracy and completeness, and preparing reports.
• Regulatory Compliance:
  Adhering to study protocols, institutional policies, and regulatory guidelines (e.g., GCP, IRB).
• Communication and
  
  Collaboration:
  
  Liaising with investigators, sponsors, and other healthcare professionals to ensure smooth trial operations.
• Monitoring and Reporting:
  Monitoring participant safety, reporting adverse events, and maintaining accurate research documentation.
• Study Logistics:
  Managing study supplies, equipment, and budgets, and coordinating with laboratories.

• Educational Background: A bachelor s degree in a scientific, health-related, or business administration field is preferred
• Organizational
  
  Skills:
  
  Strong organizational and time management skills are crucial for managing multiple tasks and deadlines.
• Communication
  
  Skills:
  
  Excellent written and verbal communication skills are needed to interact with participants, researchers, and other stakeholders
• Attention to Detail:
  Accuracy and attention to detail are essential for data collection, record-keeping, and regulatory compliance.
• Problem-Solving
  
  Skills:
  
  The ability to identify and resolve issues that may arise during the clinical trial process.
• Knowledge of Regulatory Guidelines:
  Familiarity with Good Clinical Practice (GCP) and Institutional Review Board (IRB) requirements
• Experience Requirement:
  Experience as a Coordinator in a medical office Research Department (required)