Senior Central Monitor

As a Sr. Central Monitor you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

RESPONSIBILITIES

• Activities typically include developing the Risk-Based Quality Management and Risk-Base Monitoring using PowerBI, CluePoints and TRI TRIAL OPRA Platforms for applicable studies, ensuring key risk indicators (KRIs) and data quality assessment (DQA) properly defined and set up in the system to support the study, processing and reviewing study data in the system for the signal and action management, and follow up for the issue resolution
• Review protocols to ensure the set-up, review and reporting requirements can be met and are standardized
• Provide technical oversight, guidance and coordination for all the central monitor activities
• Define key risk indicators (KRIs) in study system, and ensure consistency between the standard level and the study level
• Ensure RBM system alignment with the protocol and adherence to ICH GCP, SOPs, corporate standards and regulatory requirements
• Work with Study Team to define the issue resolution for the review of findings as signals and actions
• Develop, implement, and maintain Quality Control related documentation for RBM related activities to ensure data completeness and accuracy
• Perform central monitoring activities including review system outputs, propose suggestions for signal and action management, and follow up with study team for the action resolutions
• Work with Central Statistical Monitor and GCOMs to ensure all signals and actions are properly mitigated and RBM systems properly released
• Ensure lessons learnt during the course of the study are documented and shared with other central monitors/ study teams to facilitate cross-study learning
• Implement global strategies, initiatives, processes, and standards to ensure consistent, efficient, and quality processes to meet quality, timelines and deliverables

QUALIFICATION

• Bachelor's Degree in a scientific or business related discipline
• 3+ years' professional experience, ideally in data management/programming or other technical area
• Demonstrated knowledge of clinical development including knowledge and understanding of the principles of GCP, particularly in relation to risk-based monitoring
• Awareness of relevant data standards, e.g., CDISC, CDASH, SDTM
• Ability to critically analyze, interpret, and summarize statistical output from risk-based quality management software, e.g., CluePoints
• Ability to manage tasks, time and priorities
• Demonstrated effective verbal and written communication skills, including the ability to communicate in a remote team environment and adapt communications to audience
• Relevant pharmaceutical industry experience
• Experience with or ability to learn data visualization techniques, e.g
• Proficient experience using commercial clinical data management systems and/or EDC products
• Clinical trials expertise with an understanding of data operations required for the reporting of clinical trial data
• Good understanding of ICH and regulatory guidelines
• Working knowledge of clinical data and relevant data standards
• Strong written and oral communication skills, and project management skills
• Proven ability to operate with limited oversight
• Knowledge of at least 1 Therapeutic Area especially ONCOLOGY
• Proven ability to manage delivery under tight timelines

Why ICON?

Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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