Research Admin Specialist II-Clinical Trial Budgets

Huron•Chicago, IL

1d•$72,000 - $88,000•Remote

About The Position

Join Huron's Research Office Team as a Clinical Research Administrative Specialist II. In this role, you will assist the team in developing coverage analysis reports, study budgets, study calendars, charge segregation, and other trial documentation required for clinical research studies. You will also review projects from Clinical Research Administrative Specialist I and support client contacts for specific needs. This position offers an opportunity to expand your knowledge of clinical trial regulations and develop skills in Huron's Research Office service lines.

Requirements

U.S. work authorization is required.
Bachelor’s degree in a field related to this position or equivalent work experience.
A minimum of 3 years of clinical research administration related experience.
Experience developing clinical research budgets.
Experience in coverage analysis.

Nice To Haves

Clinical Trial budget development & negotiation experience is highly desired.
Experience in clinical trials policy and other applicable research billing rules. Experience applying the policy to clinical trial protocols for coverage determination.
Experience with conducting Quality Assurance reviews, aiming to significantly reduce the QA burden.
Background in medical coding or billing or degree in Health Information Management.
Demonstrated experience interacting with individuals at various levels in an organization and providing timely updates both from an internal and external standpoint.
Ability to contribute to innovative solutions and process improvements in clinical trial coverage analysis and budgeting.
Experience in providing guidance and training to junior staff, fostering a culture of continuous improvement and skill development.
Staying abreast of industry trends and regulatory changes to maintain expertise.

Responsibilities

Assist in developing coverage analysis reports, study budgets, study calendars, charge segregation, and other trial documentation required for clinical research studies.
Assist in review and feedback for Clinical Research Administrative Specialist I projects.
Support client contacts for client specific needs.
Expand working knowledge and experience with clinical trial regulation.
Develop strong skills in the variety of service lines Huron’s Research Office offers.