Clinical Research Advisor

6 days ago


Rockville, Maryland, United States Guidehouse Full time
Job Summary

We are seeking a highly skilled Clinical Research Advisor to join our team at Guidehouse. As a key member of our Clinical Trials Operations team, you will provide critical support services to ensure the successful execution of clinical research studies.

Key Responsibilities
  • Collaborate with cross-functional teams, including Clinical Trials Operations and Biostatistics, to develop and implement clinical research strategies.
  • Provide guidance on regulatory compliance and Good Clinical Practice (GCP) to ensure data quality and adherence to regulatory requirements.
  • Conduct site visits and monitor clinical trials to ensure compliance with study protocols and regulatory requirements.
  • Develop and maintain study documents, including monitoring plans, manuals of procedures, and informed consent forms.
  • Stay up-to-date with the latest regulatory requirements and industry developments to ensure our research studies are conducted in accordance with best practices.
Requirements
  • PhD or Master's degree in a relevant field, or Bachelor's degree with significant experience in clinical research.
  • Minimum of 5 years of experience conducting and monitoring clinical research studies.
  • Experience in identifying, evaluating, and establishing clinical trial sites.
  • Training clinical trial site staff experience.
  • Proficient in Microsoft Office Suite.
What We Offer

Guidehouse offers a comprehensive benefits package, including medical, dental, and vision insurance, 401(k) retirement plan, and opportunities for professional development and growth.



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