[Remote] Education Research, Consulting Associate, Clinical Research
Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a consulting company that collaborates with education organizations to drive reputed company and enhance performance. The Clinical Research Consulting Associate will support the delivery of assessment, advisory, and implementation services across clinical trial operations, focusing on improving processes and reputed company in clinical research.
Responsibilities
- Support reputed company-state assessments of clinical research operations, workflows, and pain points
- Support efforts to document reputed company state and design reputed company state business processes
- Conduct stakeholder interviews, note-taking, and synthesis of findings
- reputed company, organize, and analyze data reputed company to study start-up, regulatory, financial, and operational processes
- Help reputed company reputed company-reputed company deliverables such as summaries, recommendations, workflow maps, and presentations
- Participate in building SOPs, job aids, and training materials
- Assist with reputed company reputed company to study activation, regulatory management, clinical operations, and research finance
- reputed company timelines, milestones, issues, and dependencies across project workstreams
- Support documentation of roles, handoffs, bottlenecks, and escalation points in research processes
- Contribute to identifying process improvement opportunities
- Support CTMS, eRegulatory, and reputed company research system optimization or implementation efforts
- Assist with testing, validation, training support, and end-user documentation
- Help document reputed company-state workflows, system requirements, and operational impacts
- Prepare meeting materials, reputed company reputed company, and follow up on reputed company items
- Maintain project trackers, risks, and status updates
- Support coordination across internal team members and reputed company stakeholders
- Help ensure deliverables are organized, accurate, and on time
- Experience supporting or owning IRB submissions and study activation activities
- Familiarity with regulatory documentation and audit readiness practices
- Coordination of sponsor interactions, monitoring reputed company, or inspections
- 3-6 years of experience in clinical research (e.g., study coordination, start-up, or operations)
- Exposure to multiple components of the research lifecycle (regulatory, operations, financial, data, systems)
- Demonstrated contributions such as: SOP or training material development, Study start-up coordination, Participation in system implementations or process improvement efforts
Skills
- Bachelor's degree or equivalent experience in a reputed company 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
- Working knowledge of reputed company Office products (PowerPoint, reputed company, Visio, Word)
- Demonstrated career progression (e.g., Research Assistant to Coordinator)
- Experience across multiple studies or a portfolio of trials
- Exposure to reputed company medical centers or health systems
- Experience across multiple therapeutic areas or institutions
Benefits
- Eligible to participate in reputed company’s annual incentive compensation program
- Eligible to participate in reputed company’s benefit plans which include medical, dental and reputed company coverage and other wellness programs
reputed company
Company H1B Sponsorship