Clinical Insights Analyst I-RBQM

To be successful in this role, the The Clinical Insights Analyst must have Cluepoints experience, exposure to clinical trials, and working with cross functional teams.

Job responsibilities may include:

• Support other CRA team members, acting as RBQM Leads, in the identification and management of protocol, critical data and process, ‘Critical to Quality’ elements, safety and data integrity, and other protocol execution risks
• Supports cross-functional study team and RBQM Leads in Protocol Risk Assessment, risk identification and evaluation into Risk MAP, as required
• Support RBQM Leads in selection and implementation of Key Risk Indicators (KRIs), and Quality Tolerance Limit parameters (QTLs) and other applicable assessments and dashboards for each study in the RBQM system, ensuring consistency with applicable standards
• Perform the set up and maintenance of the Risk-Based Quality Management (RBQM) system based on study teams requirements, data sources and structure Perform peer reviews, QC and or Validation of study setup in RBQM system vs RBQM Plan and system specifications, as required
• Work collaboratively with assigned Programmer to implement and refine study-specific KRIs and QTLs in the RBQM system
• Performs, as required, the execution and review of the Study’s assessments and analysis, and diagnosing and explaining anomalies identified in the data and risks
• Deliver timely and high-quality risk-based monitoring analytics and supports RBQM leads in communication to the cross-functional study team and CRO (both written report and oral presentation) to identify issue resolution as required
• Support RBQM Leads during risk reviews sessions with cross-functional study team throughout clinical trials lifecycle
• Ensure appropriate status and process documentation is produced and maintained during the study including study-specific validation
• Communicate and/or escalate serious risks and issues to the cross-functional study team and/or management and Quality, as needed
• Support RBQM Lead in conducting end of trial summarization of risk management activities, including QTL and other issue findings summaries, in preparation for inclusion to clinical study report
• Ensure inspection readiness for clinical risk management and centralized monitoring activities scope of activities
• Champion RBQM within the company and participates in continuous improvement and development of risk management processes and system as needed

Qualifications

• Proven experience in a clinical research environment
• At least 4 years’ experience in a in a pharmaceutical/biologics/biotechnology company
• Working knowledge of clinical development processes, understanding concepts and principles of study design, conduct and close out, as well as clinical program develop

Qualifications

• Proven experience in a clinical research environment
• At least 4 years’ experience in a in a pharmaceutical/biologics/biotechnology company
• Working knowledge of clinical development processes, understanding concepts and principles of study design, conduct and close out, as well as clinical program develop

Skills

• Familiarity and good understanding and knowledge of clinical trials risk management concepts and principles in the Pharma or CRO industry
• Experience with data analytics and data visualization technologies
• Strong critical thinking and analytical skills and aptitude for data analytics including mathematical and statistical concepts
• High degree of accuracy and attention to detail
• Experience and understanding of clinical trial data from various sources (e.g. Clinical devices, SDTM, RAVE, IRT, etc)
• Ability to work collaboratively in a team environment whilst managing changing priorities to achieve goals/targets
• Ability to build, develop, and maintain good working relationships with internal and external cross-functional customer groups
• Excellent English oral and written communication skills

Skills

• Familiarity and good understanding and knowledge of clinical trials risk management concepts and principles in the Pharma or CRO industry
• Experience with data analytics and data visualization technologies
• Strong critical thinking and analytical skills and aptitude for data analytics including mathematical and statistical concepts
• High degree of accuracy and attention to detail
• Experience and understanding of clinical trial data from various sources (e.g. Clinical devices, SDTM, RAVE, IRT, etc)
• Ability to work collaboratively in a team environment whilst managing changing priorities to achieve goals/targets
• Ability to build, develop, and maintain good working relationships with internal and external cross-functional customer groups
• Excellent English oral and written communication skills