Clinical Research Calendar Analyst

Responsibilities

• Interpret, translate, build, and configure electronic study calendars for clinical trial data capture in accordance with the terms of the individual protocol of each specific clinical trial.
• Perform quality assurance of work product to ensure proper functionality within clinical trials management system (CTMS) while maintaining protocol accuracy.
• Interpret and identify salient information from negotiated budget and payment terms. Configure electronic study budgets for clinical trial data capture in accordance with the terms of the negotiated budget and contract payment terms.
• Perform system testing as directed and quality control of application functionality during application upgrades.
• Develop prioritization schema to aid in workload management for calendar and budget build tasks.
• Manage and process daily reports including conducting weekly audits of overdue work products.
• Update team standard operating procedure manual to maintain consistency of work product across the institution.
• Evaluate and perform periodic data clean-up via larger quality assurance projects.
• Assist the CTMS help desk team to support current end users who encounter problems or have questions via written communication as well as weekly Office Hours and one-off meeting requests.
• Collaborate with direct supervisor, coverage analysis team, budget team, clinical research team, project managers, health system representatives, consultants, and vendors to ensure overall completion of goals, schedules, and deadlines.
• Utilize several applications to communicate and manage end user interactions.
• Provide superior customer service to end users and parallel central office teams.

Qualifications

• Bachelor’s degree, preferably in Clinical Research, Science, Health Sciences, or related fields, or equivalent combination of education and related experience.
• Minimum 2 years of experience in clinical research.
• Experience reading and interpreting clinical research protocols.