Research Admin Specialist II – CTMS, OnCore

🕒 September 25

🇺🇸 United States – Remote

💵 $72k - $88k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 15%

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Huron

WebsiteLinkedInAll Job Openings

5001 - 10000 employees

Founded 2002

🏥 Healthcare

📦 Logistics

📣 Marketing

Healthcare • Logistics • Marketing

Huron Consulting Group is a global consultancy that provides a wide range of services including strategy, operations, advisory, digital, technology, and analytics solutions to various sectors such as healthcare, education, energy, and financial services. Huron helps organizations navigate complex challenges and drive growth through tailored solutions and innovative strategies. The company employs a team of experts dedicated to delivering high-impact solutions that address the unique needs of each client, focusing on areas such as managed services, outsourcing, and leadership development.

📋 Description

• Develop calendars for multiple clients, including arms, segments, procedures, and visit assignments in Clinical Trial Management Systems (CTMS) • Build financial consoles by adding protocol-related elements, parameters, specifications, subject-related items, and milestones for new and legacy clinical trials in CTMS • Develop coverage analyses for multiple clients in Excel and client CTMS • Develop research administrative back-office deliverables, including budget development and negotiation, sponsor invoicing, accounts receivable management and reconciliation, and regulatory administrative support • Review and provide feedback on Clinical Research Administrative Specialist I projects • Begin supporting client contacts for client-specific needs

🎯 Requirements

• 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 • 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

🏖️ Benefits

• Medical, dental and vision coverage • Wellness programs • Participation in Huron’s annual incentive compensation program

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