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Clinical Trials Coordinator

2 months ago

Carlsbad, United States DCN Diagnostics Full time
Job Summary

The Clinical Trials Assistant will provide critical support to the Clinical Research Services team in the management of clinical studies.

This role involves working closely with the Clinical Research team to ensure the smooth execution of clinical trials, from study setup to close-out.

Key Responsibilities
  1. Study Management: Assist in the management of study documents, including filing, tracking, and maintaining accurate records.
  2. Supply Chain Management: Ensure adequate supply of investigational products to study sites, manage inventory, and maintain accurate records.
  3. Data Review: Review clinical data for accuracy and raise queries as needed to ensure data integrity.
  4. Team Collaboration: Work closely with the Clinical Research Associates and Clinical Trial Managers to ensure day-to-day operations for studies are adequate.
  5. Communication: Interface with Data Management and Biostatistics teams as needed to ensure seamless communication and collaboration.
  6. Administrative Tasks: Perform other tasks and duties as assigned by the Clinical Research team.
Requirements
  1. Education: Associate's degree or equivalent in a related field.
  2. Experience: Industry experience as a Clinical Trials Assistant or in a lab or clinical environment preferred.
Skills and Competencies
  1. Technical Skills: Proficient in Microsoft Office products (Excel, Outlook, PowerPoint, and Word) and desktop publishing software.
  2. Communication Skills: Strong interpersonal, presentation, and communication skills.
  3. Organizational Skills: Good organizational, problem-solving, and analytical skills; able to manage priorities, projects, and workflow.
  4. Attention to Detail: Attention to detail, with a commitment to excellence and high standards.
  5. Teamwork: Ability to work effectively in a team environment, with a proactive, motivated, and focused attitude.