Job Overview: As one of the world's largest and most comprehensive drug development services companies, LabCorp Drug Development has helped pharmaceutical and biotech companies develop one-third of all prescription drugs in the marketplace today.About the position: The Clinical Trial Data Analyst (Global Monitor) will create and maintain the Global Monitoring plan for the assigned studies, coordinate the work of Client Coordinator Specialists, Global Monitoring Center, and Regional Study Coordinators, and ensure regular communication with the Global Study Managers or Global Study Leads who are accountable for the entire protocol.Responsibilities/Duties: Leverages therapeutic area, client, and study type knowledge to create and maintain a study-specific monitoring and data lock plan.Liaise with CCLS internal teams to ensure monitoring needs for a study can be met with quality.Ability to create and motivate a team around project deliverables.Demonstrates strong attention to detail.Provides data-focused impact assessments as needed.Triage of new work requests.Liaise with Developers to ensure development of monitoring tools are completed to the client's specifications.Delegates/generates reports related to monitoring activities.Reviews/analyzes data within monitoring scope.Suggests actions/changes to GSM based on data analysis.Escalates issues, highlights trends and liaises closely with Global Study Manager or Global Study Lead throughout the life of the study to ensure monitoring is appropriate.Supports Risk Management Plan creation and ongoing maintenance through monitoring and analysis.Able to act efficiently in an environment with dynamic timelines and priorities.Participate in functional meetings (e.G. CLFs) and provide input, keeping processes up to date.Comply with CCLS Global Project Management strategy.Support a culture of continuous improvement, quality, and productivity.Education/Qualifications: University Degree required; Masters or PhD in a scientific field preferred.Experience: 5-7 years of related experience (Education can substitute for work experience) in project management, data analysis for the pharmaceutical/healthcare industry. Demonstrated advanced level knowledge of Excel, Access, and other monitoring tools.Curious, data-driven analytical thinker with a high degree of motivation, flexibility, and creativity. Big picture thinker who suggests changes to process, identifies risks, and potential opportunities for data improvement. Strong problem-solving skills. Able to operate with minimal guidance while owning deliverables end-to-end. Proven ability to effectively communicate ideas/concepts and to motivate others to accomplish challenging shared goals and objectives. Dedication to learning and self-improvement. Robust self-organization; at ease with managing conflicting priorities. Strong customer service skills. Working proficiency in English.#J-18808-Ljbffr
