[Hiring] Research Admin Specialist II-CTMS (OnCore) @Huron

Role Description

You’ll help our clients to achieve organizational effectiveness, improve student outcomes, implement new technologies and align resources and investments to ensure long-term sustainability.

As a Clinical Research Administrative Specialist II, you’ll assist Huron’s Research Office team in:

• Developing coverage analysis reports
• Creating study budgets
• Formulating study calendars
• Charge segregation
• Preparing other trial documentation required for clinical research studies, including industry, federally sponsored, and locally (investigator) sponsored research
• Assisting in review and feedback for Clinical Research Administrative Specialist I projects
• Supporting client contacts for client specific needs

You’ll have the opportunity to expand upon your working knowledge and experience with clinical trial regulation, and to develop strong skills in the variety of service lines Huron’s Research Office offers.

Qualifications

• U.S. work authorization is required
• Bachelor's degree required in a health/science related discipline (biology, public health, healthcare administration, nursing, etc.) or equivalent professional experience
• A minimum of 3 years of clinical research administration related experience including exposure to coverage analysis, clinical trial budgeting, and/or CTMS calendar or financial console development
• Ability to interpret and apply clinical guidelines including Centers for Medicare and Medicaid, Federal Drug Administration, National Comprehensive Cancer Network
• Highly detail oriented with the ability to provide quality assurance or develop back-office research related deliverables with minimal to no errors
• Intermediate Excel competency

Requirements

• This is a full time US-REMOTE role
• This salaried position may require working additional hours at times, depending on business needs

Preferred Qualifications

• Experience with at least one of the following CTMS / CRMS is preferable:
  • Forte Research System’s OnCore™
  • Study Manager’s Reveal
  • Velos’s eResearch and Patient Protocol Manager
• Experience with conducting Quality Assurance reviews
• Experience developing others including providing training for new skills
• Experience drafting standard operating procedures or other process documents

Position Level

Senior Analyst

Country

United States of America