Job Description

Title: Clinical Data Manager Location: Maple Grove, MN Duration: 8 Month Summarize the main purpose of the role. The Clinical Data Manager is responsible for managing the development, documentation, and execution of risk-based quality management systems, as described in the risk assessment, data management plan, and site and central monitoring plans. As the customer‑face of Data Review and its primary liaison with the therapy group, the Clinical Data Manager's therapy‑specific knowledge ensures alignment to customer definitions of criticality and informs review and analysis of study data. Roles and responsibility: Identification of study specific risks to study conduct and human subject safety; analysis of risks; development and implementation of mitigation strategies. Review of study data to detect anticipated and unanticipated issues related to trial data completeness and quality. Facilitate multi‑stakeholder discussions to review findings, evaluate impact and develop action plans for correction and continued monitoring. Conduct Central Monitoring activities, as described in Central Monitoring Plan. Direct all data cleaning activity related to assigned studies. Education Bachelor's Degree (± 16 years) Biology, Health Sciences, Mathematics, Computer Science, or equivalent. Experience: 3 years in clinical operations or healthcare related field. Education and work experience in project management, life sciences and/or technical field. Knowledge of data collection best practices for clinical trials. Knowledge of global clinical operations. Experience in consultative role, with Subject Matter Expertise, and effectively influencing a team decision to the desired outcome. Proficient at the identification of risks in a process, evaluation of likelihood and impact, and the development of effective mitigation and monitoring strategies that are imperfect yet meet the business need. Proficient in the translation of clinical trial requirements to the technical specifications required for effective data collection. Skilled at making inferences and connections based on limited information, clearly describing the knowns, unknowns, and alternative explanations. Intermediate project management skills; developing a multifaceted plan with complex dependencies and holding peers accountable to adherence to the plan while maintaining positive and collaborative relationships. Intermediate therapy specific knowledge of anatomy, physiology, pathophysiology, therapy and device. Licenses and Certifications None required; Certified Clinical Data Manager (CCDM) or equivalent nice to have. Consultants Eligible Benefits Upon Waiting Period: Medical and Prescription Drug Plans Dental Plan Vision Plan Health Savings Account (for High‑Deductible Health Plans) Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit) Supplemental Life Insurance Short Term Disability (coverage varies by state) Long Term Disability Critical Illness, Hospital coverage, Accident Insurance MetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance 401(k) Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life‑changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines. Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life‑changing breakthroughs, performing key duties to create life‑changing breakthroughs. #J-18808-Ljbffr Abbott

Job Tags

Similar Jobs