
Clinical Research Project Coordinator
Posted 3 days ago

Posted 3 days ago
This is a fully remote position, open to applicants in Utah.
• Provide support for research projects requested by various departments.
• Oversee routine to moderately complex research projects, managing all related communication and documentation.
• Assist clinical research studies and departments throughout the Intermountain system.
• Coordinate submissions to IRB/HRPP and support research oversight committees and programs, or manage administrative and technical functions for grants, contracts, and external funding agreements.
• Define, develop, and implement clinical research project plans, work plans, and schedules.
• Identify resources, roles, and responsibilities for the assigned studies.
• Facilitate feedback from key participants and actively participate as a team member.
• Create budgets and scope documents for clinical research studies.
• Assist with business cases, proposals, budgets, and necessary internal and external routing forms.
• Analyze study requirements and communicate any impacts to stakeholders.
• Engage in quality assurance plans and reviews.
• Document deliverables, track and communicate timelines, and prepare reports and presentations.
• Support research billing by reviewing research accounts and reconciling invoices.
• Manage study startup, maintenance, and closeout processes.
• Provide assistance to study teams regarding study financials and serve as a subject-matter expert and liaison.
• Offer backup support as a clinical research coordinator when needed.
• Develop Medicare Coverage Analysis documents, review reimbursement guidelines, ensure accurate billing, and provide coverage reviews.
• Coordinate project assessments and response planning.
• Communicate risks, develop and implement mitigation strategies, and lead auditing activities for compliance.
• Prior experience in supporting clinical research involving human subjects.
• Experience in a role that requires effective organizational skills, follow-through, a commitment to excellence, and professional communication.
• Strong interpersonal abilities and a capacity to communicate clearly and professionally with personnel at all levels.
• Proven experience working in a collaborative team environment.
• Proficiency in using word processing, spreadsheet, database, internet, email, and scheduling applications.
• Willingness and ability to travel within the Intermountain system and work from various locations as assigned.
• Occasional overnight travel may be necessary.
• Clinical licensure, experience, or certification may be required due to grant funding stipulations.
• Bachelor’s Degree in a clinical or life science field, business, or healthcare operations from an accredited institution.
• Two years of experience in a research or relevant healthcare/business role that demands strong attention to detail and compliance with policies and procedures, or three years of such experience.
• Preferred: Experience in a clinical research setting, including relevant study management experience.
• Preferred: Experience in a healthcare or hospital environment.
• Competitive benefits package that includes wellness, health, security, connection, and engagement programs.
• Options for remote work.
• Flexible scheduling during core business hours.
• Company-provided equipment and remote work support as outlined in remote work expectations.
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