Regulatory Specialist I, Gerontology

Callowayhealth

Wake Forest University, North Carolina, US
$26.55 - $39.85 ph
Hybrid
Clinical trial regulatory compliance
Fda-regulated clinical trials
Irb standard operating procedures
Performs administrative and coordinative work directed toward the design, implementation, evaluation and review of assigned clinical trials by working closely with Principal Investigators (PI) and other Clinical Protocol and Data Management (CPDM) staff members

Job Summary

  • Performs administrative and coordinative work directed toward the design, implementation, evaluation and review of assigned clinical trials by working closely with Principal Investigators (PI) and other Clinical Protocol and Data Management (CPDM) staff members.
  • Responsible for the planning, development, implementation and evaluation of certain phases of the assigned studies.
  • Advocate Health offers a comprehensive suite of Total Rewards: benefits and well-being programs, competitive compensation, generous retirement offerings, programs that invest in your career development and so much more.

Matching Summary

Performs administrative and coordinative work directed toward the design, implementation, evaluation and review of assigned clinical trials by working closely with Principal Investigators (PI) and other Clinical Protocol and Data Management (CPDM) staff members.

Salary

$26.55 - $39.85

Skills & Requirements

Must-have

  • Clinical trial regulatory compliance
  • FDA-regulated clinical trials
  • IRB Standard Operating Procedures
  • Good Clinical Practice adherence
  • Maintain study regulatory files
  • OnCore (WISER) system proficiency

Nice-to-have

  • Budget and financial tracking
  • Patient accounting experience
  • Foster positive image
  • Intercultural relations sensitivity

Key Requirements

  • Bachelor's degree required
  • Two years research experience
  • CITI certification required
  • SOCRA or ACRP Certification preferred

Work Rights

Not specified

Tailored Resume

Cover Letter