Clinical Research Regulatory Specialist

2 weeks ago


Temecula, California, United States Viking Clinical Research Full time
Job Opportunity

Viking Pharmaceutical Trials is seeking a highly skilled Clinical Research Regulatory Specialist to join our team.

Key Responsibilities:

  • Provide regulatory expertise in clinical trials, with a focus on CNS studies.
  • Develop and maintain site guidelines, IRB submissions, and protocol version updates.
  • Oversee site training, including GCP and annual/bi-annual training.
  • Prepare sites for monitoring and audit visits.
  • Manage study-start-up materials and create ISF Binders.
  • Maintain systematic and organized documentation throughout clinical trials.

Requirements:

  • Strong verbal and written communication skills.
  • Ability to work independently and in a team environment.

Salary: Competitive salary based on experience.

Relocation: Out-of-state applicants, please provide a cover letter explaining relocation plans and timeline.



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