Research Compliance Specialist II

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

📋 Description

• Assess and prioritize incoming IRB submissions and COI disclosures.

• Perform a preliminary review of IRB submissions for federal agency oversight, missing documents, and specific regulatory concerns.

• Carry out specific non-committee IRB evaluations, including not-human-research classifications and exempt determinations.

• Facilitate the COI disclosure process, which includes initiating disclosure cycles and addressing any delays in disclosures.

• Review COI disclosures in relation to research portfolios and institutional obligations.

• Identify disclosures that need attention from the COI Committee or leadership.

• Prepare COI management plans.

• Provide support to universities, academic medical centers, and hospitals throughout the United States.

• Manage multiple clients simultaneously while collaborating with Huron’s Research Office team.

⛳️ Requirements

• U.S. work authorization is mandatory.

• A Bachelor’s degree or equivalent professional experience is required.

• At least 2 years of combined experience in IRB and COI processes.

• Proficient in Microsoft Word, Adobe Acrobat, and other Microsoft Office applications.

• Strong expertise in Microsoft Excel.

• Familiarity with electronic IRB and COI submission/review platforms.

• Understanding of federal regulations that govern ethical research practices and human-subject protection.

• Knowledge of federal conflict-of-interest regulations.

• Effective time management skills to adhere to deadlines.

• Capable of multitasking and supporting various internal initiatives.

• Exceptional oral and written communication abilities.

• Quick learner with a keen attention to detail.

🏝️ Benefits

• Annual incentive compensation program.

• Medical coverage.

• Dental coverage.

• Vision coverage.

• Wellness programs.

• Full-time salaried position.