98 applicants

Company

Huron · 18 hours ago

Research Admin Specialist II- CTMS/OnCore, Flexible Location

Chicago, IL

Full-time

Remote

Mid Level

$72K/yr - $88K/yr

3+ years exp

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ConsultingInformation Technology

No H1B

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Responsibilities

Calendar development for multiple clients including the creation of arms, segments, procedures, and visit assignments in accordance with Huron and industry standards in Clinical Trial Management Systems ("CTMS").

Financial console build including adding protocol related elements, parameters, specifications, subject related items, and milestones for both new and legacy clinical trials in CTMS.

Coverage Analysis development for multiple clients in accordance with Huron and industry standards both in Excel and in client CTMS.

Other research administrative back-office deliverable development including by not limited to, budget development and negotiation, sponsor invoicing, account receivable management and reconciliation, and regulatory administrative support.

Qualification

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Clinical research administrationCTMS calendar developmentCoverage analysisClinical trial budgetingExcelQuality assurance reviewsTraining developmentHealth/science degreeRegulatory supportStandard operating procedures

Required

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.

Preferred

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

Other wellness programs

Company

Huron

Glassdoor

4.0

Huron is a global professional services firm that collaborates with clients to put possible into practice by creating sound strategies, optimizing operations, accelerating digital transformation, and empowering businesses and their people to own their future.

Founded in 2002

Chicago, Illinois, USA

5001-10000 employees