Research Admin Specialist II – CTMS, OnCore

atHuronRemoteUS flagUnited StatesFull-timeUncategorizedMid-levelSenior$72k – $88k/year

Posted Sep 25

This is a fully remote position, open to applicants in United States.

πŸ“‹ Description

β€’ Create calendars for various clients, encompassing arms, segments, procedures, and visit assignments within the CTMS.

β€’ Construct financial consoles by incorporating protocol-related components, parameters, specifications, subject-related items, and milestones for both new and existing clinical trials in CTMS.

β€’ Prepare coverage analyses for multiple clients using Excel and client CTMS.

β€’ Generate research administrative back-office deliverables, including budget formulation and negotiation, sponsor invoicing, accounts receivable management and reconciliation, as well as regulatory administrative assistance.

β€’ Collaborate with Huron's Research Office team on coverage analysis reports, study budgets, study calendars, charge segregation, and other trial documentation.

β€’ Review and provide constructive feedback on projects managed by Clinical Research Administrative Specialist I.

β€’ Assist client contacts with specific needs.

β€’ Enhance understanding of clinical trial regulations and develop skills across Huron's Research Office service offerings.


⛳️ Requirements

β€’ U.S. work authorization is mandatory.

β€’ A bachelor's degree in a health/science-related field (such as biology, public health, healthcare administration, nursing, etc.) or equivalent professional experience is required.

β€’ A minimum of 3 years of experience in clinical research administration, including exposure to coverage analysis, clinical trial budgeting, and/or CTMS calendar or financial console development.

β€’ Capability to interpret and apply clinical guidelines, including those from the Centers for Medicare and Medicaid Services, Food and Drug Administration, and National Comprehensive Cancer Network.

β€’ Strong attention to detail with the ability to ensure quality assurance or create back-office research deliverables with minimal to no errors.

β€’ Intermediate proficiency in Excel.

β€’ Preferred: Experience with OnCore, Reveal, Velos's eResearch, or Patient Protocol Manager.

β€’ Preferred: Experience in Quality Assurance reviews.

β€’ Preferred: Experience in mentoring others and providing training for new skills.

β€’ Preferred: Experience in drafting standard operating procedures or other process documentation.


🏝️ Benefits

β€’ Annual incentive compensation program.

β€’ Medical coverage.

β€’ Dental coverage.

β€’ Vision coverage.

β€’ Wellness programs.

β€’ Salaried position.

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