Senior Clinical Research Associate

1 week ago

Los Angeles, California, United States Cognitive Research Corporation Full time $100,000 - $150,000 per year

Overview

Clinical Research Associate is responsible for tracking and maintaining study specific non-CRF databases and administrating clinical research projects. This is accomplished by collecting documentation, site management, clinical contact, and reviewing CRF's. The CRA is also responsible for maintaining relationships with investigators. The ideal candidate must be willing to traveling to various worksites.

Key Responsibilities:

  • Maintain a strong relationship with each Investigator and clinical site staff.
  • Able to handle 8 Monitoring Days on-site per month
  • Initiate, monitor, and close-out investigative sites in accordance with FDA/ICH regulations.
  • Track and maintain study specific non-Case Report Form database
  • Administer Clinical research projects; collect investigator documentation, site management, clinical contact, and prepare monthly status reports.
  • Review Case Report Forms to identify erroneous, missing, or incomplete data.
  • Generate data queries to resolve problematic data to appropriate personnel, and review responses to assure the database is updated accordingly.
  • Report, write narratives, and follow-up on reported serious adverse events.
  • Verify study drug accountability; generate and track drug shipments and storage.
  • Travel as necessary, based on project needs.
  • Participate in the development of protocols and Case Report Forms.
  • Perform data collection, retrieval, entry and clean up as necessary.
  • Negotiate study budgets with potential investigators.
  • Independently manage sites confirming clinical study site operations are completed under site procedures
  • Perform other duties as assigned by management.

Qualifications:

  • BS/BA in appropriate field (e.g. Life Sciences, Pharmacy, or Nursing) or applicable education with relevant experience.
  • 4 years CRA experience
  • Ability to handle 8 Monitoring Days on site a month
  • Experience in monitoring CNS indications, and Study Coordinator in CNS
  • Comfortable supporting Phase 1 programs
  • Experienced with numerous EDC system
  • Experience in the pharmaceutical industry or hospital setting is preferable.
  • Ability to work and travel independently with minimal supervision.
  • Self-motivated attitude.
  • Computer competency (Microsoft Word and Excel)
  • Good communication skills. Good command of written English.
  • Meticulous attention to details.

Join us as we make significant strides in the field of clinical research Your contributions will not only advance scientific knowledge but also improve patient outcomes worldwide.

Job Type: Full-time

Pay: $125, $150,000.00 per year

Benefits:

  • 401(k)
  • Dental insurance
  • Flexible schedule
  • Flexible spending account
  • Health insurance
  • Health savings account
  • Life insurance
  • Paid time off
  • Referral program
  • Retirement plan
  • Vision insurance

Work Location: Remote

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