Job
Description
Role Overview: You will be responsible for performing the technical configuration of the CluePoint Central Monitoring Platform solution for clinical studies based on requirements. Your role will involve leading the technical study level set-up, supporting ongoing refreshes based on defined frequency, creating templates, leading Prep Meetings with CM to review analysis set-up and dashboards in preparation for study team meetings, creating dashboards (e.g., KRI, DQA, QTL, SPOT, etc.), managing study configuration, supporting CM in defining study requirements, ensuring pre-processing activities are complete (e.g., data availability (pre-defined)), and creation of study. Key Responsibilities: - Perform the technical configuration of the CluePoint Central Monitoring Platform solution for clinical studies based on requirements. - Lead technical study level set-up. - Support ongoing refreshes based on defined frequency. - Create templates. - Lead Prep Meetings with CM to review analysis set-up and dashboards in preparation for study team meetings. - Create dashboards (e.g., KRI, DQA, QTL, SPOT, etc.). - Manage Study Configuration. - Support CM in defining study requirements. - Ensure pre-processing activities are complete (e.g., data availability (pre-defined)). - Create studies. Qualifications Required: - Relevant experience in technical configuration for clinical studies. - Strong understanding of Central Monitoring Platform solutions. - Proficiency in creating templates and dashboards. - Ability to manage study configuration effectively. - Excellent communication and teamwork skills. Role Overview: You will be responsible for performing the technical configuration of the CluePoint Central Monitoring Platform solution for clinical studies based on requirements. Your role will involve leading the technical study level set-up, supporting ongoing refreshes based on defined frequency, creating templates, leading Prep Meetings with CM to review analysis set-up and dashboards in preparation for study team meetings, creating dashboards (e.g., KRI, DQA, QTL, SPOT, etc.), managing study configuration, supporting CM in defining study requirements, ensuring pre-processing activities are complete (e.g., data availability (pre-defined)), and creation of study. Key Responsibilities: - Perform the technical configuration of the CluePoint Central Monitoring Platform solution for clinical studies based on requirements. - Lead technical study level set-up. - Support ongoing refreshes based on defined frequency. - Create templates. - Lead Prep Meetings with CM to review analysis set-up and dashboards in preparation for study team meetings. - Create dashboards (e.g., KRI, DQA, QTL, SPOT, etc.). - Manage Study Configuration. - Support CM in defining study requirements. - Ensure pre-processing activities are complete (e.g., data availability (pre-defined)). - Create studies. Qualifications Required: - Relevant experience in technical configuration for clinical studies. - Strong understanding of Central Monitoring Platform solutions. - Proficiency in creating templates and dashboards. - Ability to manage study configuration effectively. - Excellent communication and teamwork skills.
