Study Manager and Coordinator

3 weeks ago


Dallas, Texas, United States Wake Research Full time
Job Responsibilities:
The Clinical Research Coordinator will play a critical role in the conduct of the study, managing daily clinical trial activities, and coordinating with site management and Principal Investigators. Key responsibilities include:
  • Assisting trial Investigator in screening and review of potential study participants' eligibility
  • Maintaining case report forms, charts, and documentation
  • Mentoring, training, and high-level oversight of other clinical research coordinators and research assistants
  • Ensuring that all clinical activities are carried out in accordance with established research protocol and standards in compliance with all applicable laws, regulations, policies, and procedural requirements

Qualifications:
To be successful in this role, you should have a Clinical Research Coordinator certification, 1-2 years of experience in a similar position, and a strong understanding of GCP Certification and Advanced CRC principles. Additionally, you should be able to maintain strict confidentiality of patients, employees, and company information at all times and adhere to HIPAA Guidelines.

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