Clinical Research Admin: CTMS & Budgets

Huron; United States; Remote; USD 72,000 - 88,000; Full time

Benefits offered by this job

Medical coverage

Dental coverage

Vision coverage

401(k) plan with employer match

Stock purchase plan

Paid time off

Parental leave and adoption assistance

Wellness program

Job summary

Huron’s Research Office Team is seeking a Clinical Research Administrative Specialist II to support development of coverage analyses, study budgets, and trial documentation for various research programs. You will contribute to CTMS calendars, budget negotiations, and regulatory support, collaborating with client contacts and internal teams.

The role emphasizes accuracy, adherence to clinical guidelines (FDA/ CMS/ NCCN), and strong Excel skills, with remote work possibilities in the US and a

Qualifications

• U.S. work authorization is required.
• Bachelor's degree required in health/science related discipline or equivalent professional experience.
• A minimum of 3 years of clinical research administration related experience including exposure to coverage analysis, budgeting, and CTMS calendar or financial console development.
• Ability to interpret and apply clinical guidelines including CMS, FDA, NCCN.
• Highly detail oriented with the ability to deliver back-office research deliverables with minimal errors.
• Intermediate Excel competency.

Responsibilities

• Calendar development for multiple clients in CTMS.
• Financial console build for protocol related elements and milestones in CTMS.
• Coverage Analysis development in Excel and CTMS.
• Budget development, sponsor invoicing, accounts receivable management and reconciliation, regulatory support.

Skills

Clinical trial budgeting

CTMS calendar development

Financial console development

Detail oriented

Excel proficiency

Education

Bachelor's degree in health/science related discipline

Tools

Forte OnCore

Reveal

Velos eResearch

Patient Protocol Manager

Job description

Huron’s Research Office Team is seeking a Clinical Research Administrative Specialist II to support development of coverage analyses, study budgets, and trial documentation for various research programs. You will contribute to CTMS calendars, budget negotiations, and regulatory support, collaborating with client contacts and internal teams.

The role emphasizes accuracy, adherence to clinical guidelines (FDA/ CMS/ NCCN), and strong Excel skills, with remote work possibilities in the US and a