Lead end-to-end Clinical Data Management activities for assigned clinical studies.
Ensure clinical data are accurate, complete, consistent, and inspection-ready.
Drive proactive risk identification, issue escalation, and resolution across study teams and vendors.
Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. They are committed to transforming the future of treatment for autoimmune disease, guided by core values and focused on innovation.
Primary DM contact for assigned clinical project(s) / program(s), ensuring that tasks are performed in a timely manner.
Oversee project data entry process including development of data entry guidelines, training, data entry quality and resourcing.
Develop CRF specifications from the clinical study protocol and coordinate the review/feedback from all stakeholders.
Precision for Medicine integrates clinical trial execution with scientific knowledge, laboratory expertise, and advanced data sciences to improve the speed, cost and success rate of bringing therapies to patients. They are expanding in Asia Pacific.
Lead a large clinical study or a series of related studies with minimum guidance.
Provide mentoring and training to lower-level Data Management staff assigned to your studies.
Develop or lead the development of the Data Management Plan for a clinical study.
Parexel provides Clinical and Consulting solutions to the world’s life sciences industry. They have a global breadth of clinical, regulatory and therapeutic expertise, and a proven track record spanning 40+ years.
Perform ongoing clinical data review to ensure data quality, consistency, and completeness.
Identify discrepancies and raise/resolve queries in EDC systems.
Review patient data including eligibility, medical history, treatment, safety data, and outcomes.
Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. They partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity and anticipate change.
Partner with Clinical Operations leadership to support clinical trial execution.
Lead site feasibility, selection, initiation, and greenlight activities for clinical trial sites.
Provide guidance and oversight to CRAs, including trip report review and training support.
Immatics is dedicated to making a significant difference in the lives of cancer patients. They are a global frontrunner in precision targeting of PRAME, found in over 50 cancers, with cutting-edge science and a strong clinical pipeline.