Education Research, Consulting Associate, Clinical Research
New
United StatesFull-TimeMiddle
Salary$105,000 - $120,000
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Job Details
- Experience
- 3-6 years
- Required Skills
- Microsoft ExcelProcess improvementPowerPoint
Requirements
- Bachelor’s degree or equivalent experience in a related field.
- 3–6 years of experience in clinical research or research administration.
- Working knowledge of study start-up, IRB processes, and clinical trial operations.
- Experience using CTMS and/or eRegulatory systems.
- Strong organizational, analytical, and communication skills.
- Proficiency in Microsoft Office products including PowerPoint, Excel, Visio, and Word.
- Experience supporting or owning IRB submissions and study activation activities.
- Familiarity with regulatory documentation and audit readiness practices.
- Experience coordinating sponsor interactions, monitoring visits, or inspections.
Responsibilities
- Support current-state assessments of clinical research operations, workflows, and pain points.
- Conduct stakeholder interviews, synthesize findings, and develop client-ready deliverables like recommendations and workflow maps.
- Assist with projects related to study activation, regulatory management, and research finance.
- Support CTMS, eRegulatory, and related research system optimization or implementation efforts.
- Maintain project trackers, manage risks, and follow up on project action items.
- Participate in building SOPs, job aids, and training materials.
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