Perform EDC validation UAT, data listings review, data issues tracking and query management, external data reconciliation, data listings review coordination.
Accountable for on-time and comprehensive review of clinical study data listings
Manages the effective communication of data issues and discrepancies to study sites via the query management process.
Provides validation and UAT support for Clinical Data Management activities across studies.
Leads and coordinates functions for multiple assigned projects related to the planning, execution, collection, and cleaning of clinical data.
Works within the company’s SOPs, guidelines and standards to ensure data integrity at all times.
Iovance Biotherapeutics is committed to cultivating and offering a diverse and inclusive work environment. As an equal-opportunity employer, their employees and applicants will be considered without regard to an individual’s race, color, religion, sex, pregnancy, national origin, age, physical and mental disability, marital status, sexual orientation, gender identity, gender expression, genetic information, military and veteran status, and any other characteristic protected by applicable law.
Ensuring the data from visits is uploaded to the platform within a specific timeline.
Reviewing project data within a specific timeline and delivering data in a timely manner to key stakeholders.
Requesting and managing source/data corrections as needed.
Hawthorne Health is a leading community site network and home research visit solution provider. With 20+ sites and more than 2,000 research experienced healthcare professionals across the U.S., they leverage technology to accelerate patient access, improve retention, and reduce study costs.
Responsible for timelines and quality of CDM deliverables for the assigned studies.
Manages CDM timelines to coordinate and synchronize deliverables with the overall study timelines.
Responsible for the accuracy and completeness of the clinical data collected during a clinical trial.
Celcuity is a clinical-stage, publicly traded biotechnology company seeking to extend the lives of cancer patients through the development of targeted therapies. They are committed to fair and equitable compensation practices and strive to provide employees with competitive total compensation packages.
Maintains responsibility of assigned projects and ensures on-time delivery.
Provides input and guidance to the design of clinical databases.
Develops, tests, and validates programs and clinical databases.
Precision Medicine Group is committed to improving the efficiency of medical treatments. They focus on applying precision medicine, supported by data, to enhance research and development in the healthcare sector and is an equal opportunity employer.