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Clinical Trials Data Specialist

2 months ago

Vancouver, British Columbia, Canada PHSA Full time

Data Management for Clinical Research

As a vital member of our team, you will play a crucial role in ensuring the accuracy and integrity of data collected during clinical trials. Your responsibilities will encompass a wide range of tasks, from organizing study documentation to inputting patient information into our systems.

Key Responsibilities:

  • Maintain meticulous records and ensure compliance with established protocols and regulatory guidelines.
  • Collaborate with researchers and clinicians to collect and verify data for clinical trials.
  • Contribute to the development and refinement of data collection tools and regulatory documentation.
  • Manage user accounts and access permissions within our data management systems.
  • Generate comprehensive case report forms and ensure timely submission.
  • Retrieve and analyze data based on specific criteria, ensuring accuracy and completeness.
  • Participate actively in quality improvement initiatives to enhance data integrity and efficiency.

Qualifications:

  • Completion of a recognized Health Record Administration Program or equivalent.
  • Proven experience in data capture and management within a clinical research setting.
  • Solid understanding of ICH Guidelines and other relevant regulatory requirements.
  • Exceptional attention to detail, strong analytical skills, and excellent interpersonal communication abilities.

What We Offer:

  • Opportunities for professional growth and development within a dynamic healthcare environment.
  • A comprehensive benefits package that supports your well-being.
  • Flexible work arrangements to promote work-life balance.
  • Commitment to fostering diversity, equity, and inclusion in our workplace.