Patient Insights Manager
Posted 2 days ago
Posted 2 days ago
This is a fully remote position, open to applicants in North Carolina, +1 more state.
• Oversee the implementation of SPFQ across designated clinical studies.
• Maintain plans for implementation, timelines, milestones, risks, and action logs.
• Act as the primary operational contact for study teams and vendors on a daily basis.
• Supervise vendor deliverables and escalate any performance or quality issues.
• Ensure that all necessary documentation is complete, up-to-date, and traceable.
• Manage data collection, aggregation, and routine reporting processes.
• Perform descriptive analyses and trend reviews utilizing established methods and templates.
• Compile participant feedback and identify recurring themes, potential burden signals, and operational risks.
• Create reports and presentations for PCDE and study team evaluations.
• Collaborate with analytical or technical experts when advanced statistical analysis is needed.
• Implement established thresholds and escalation pathways effectively.
• Record recommendations, decisions, responsible parties, and follow-up actions.
• Monitor the execution of agreed actions and summarize results.
• Bring significant participant experience or trial execution signals to the attention of the PCDE lead.
• Assist in the development and maintenance of work instructions, templates, process maps, and training materials.
• Suggest process enhancements based on implementation experiences.
• Adhere to applicable GCP, privacy, data integrity, and internal quality standards.
• Keep operational documentation ready for inspection and assist in audits or inspections as needed.
• Track metrics such as response rates, completion rates, timeliness, recurring themes, and action closure.
• Support regular program reviews and discussions aimed at continuous improvement.
• Provide operational data to aid in evaluating SPFQ value and scalability.
• Assist the lead of Patient Centered Development & Experience as required.
• Approximately 3–5 years of pertinent experience in clinical research, clinical operations, patient engagement, project management, or similar fields.
• Proven experience in coordinating cross-functional activities and managing external vendors.
• Preferred experience in reviewing survey, participant feedback, patient-reported, or operational data.
• Ability to conduct descriptive analysis and recognize trends.
• Advanced statistical or data science skills are advantageous but not mandatory.
• Proficient in Excel, data visualization, and presentation software.
• Experience with Power BI or Tableau is beneficial but not essential.
• Familiarity with ICH-GCP, privacy, documentation, and data integrity principles.
• Excellent organizational, communication, issue management, and follow-up skills.
• Highly self-motivated and proactive, capable of independent work, exercising sound judgment, managing competing priorities, and driving deliverables forward with suitable autonomy.
• Legal authorization to work in the country where the position is based.
• Competitive base salary along with performance-related incentives.
• Health and wellness programs, including medical, dental, and vision coverage when applicable.
• Retirement and pension plans.
• Life insurance and disability coverage.
• Employee assistance programs and wellness resources.
• Opportunities for learning and development through structured training and career pathways.
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