**All the benefits and perks you need for you and your family:** + Benefits from Day One + Paid Days Off from Day One + Student Loan Repayment Program + Career Development + Whole Person Wellbeing Resources + Mental Health Resources and Support **Our promise to you:** Joining AdventHealth is about being part of something bigger. It’s about belonging to a community that believes in the wholeness of each person, and serves to uplift others in body, mind, and spirit. AdventHealth is a place where you can thrive professionally, and grow spiritually, by Extending the Healing Ministry of Christ. Where you will be valued for who you are and the unique experiences you bring to our purpose-minded team. All while understanding that **together** we are even better. **Schedule:** Full Time **Shift** : M-F, generally 8am -5pm **Location:** 400 CELEBRATION PLACE, Celebration, 34747 + Established in 1997 and now a 203-bed hospital + AdventHealth Celebration Health was designed as a Mediterranean resort-style facility to serve as a cornerstone of health in Disney’s planned community of Celebration, Florida + The hospital consistently delivers a state-of-the-art healing environment to residents of Osceola, Orange, Polk and Lake Counties, as well as to visitors from across the United States and the world. All within a 'living laboratory' of groundbreaking, research-driven clinical solutions that integrate mind, body and spirit in the defeat of illness and disease **The role you’ll contribute:** The Clinical Research Data Coordinator I is primarily responsible for the completeness, timely delivery, and quality of clinical research data via data entry. In this role, the Clinical Research Data Coordinator I collaborates with study Investigators, Clinical Research Coordinator(s) (CRC), study sponsors, and other research and clinical team members in the conduct of Phase I-IV industry-sponsored, grant funded (federal or other grants), and/or investigator-initiated clinical trials in accordance with trial protocols, Food and Drug Administration (FDA) regulations, and International Conference on Harmonization/Good Clinical Practices (ICH/GCP) Guidelines to meet study-specific goals and timelines as well as assist the study team with the operational needs of specific protocols to meet these goals. Actively participates in outstanding customer service and accepts responsibility in maintaining relationships that are equally respectful to all. **The value you’ll bring to the team:** + Managing and ensuring the accurate and timely retrieval and electronic data entry submission of protocol driven data points to relevant research sponsors/organizations within the specified time frame. + Abstracts and records essential physical and test data from internal and external sources. + Maintains a tracking system of study participants at the relevant time points as deemed necessary. + Conducts follow up visits and data searches, as assigned, to maintain smooth operational flow. + Prepares and provides participant status reports to leadership as requested. + Completes and maintains sponsor training and certifications on protocol-specific Electronic Data Capture (EDC) systems and portals (e.g., Medidata RAVE, Oracle, Inform, REDCap, etc.). + Actively contributes to ongoing research activities including meeting with the study sponsor monitors, CRCs and Principal Investigators to review study data and resolve data queries. Qualifications **The expertise and experiences you’ll need to succeed:** + Bachelor’s degree in healthcare related field, data processing or related field, OR + Associate degree in health science, or related field, and one year of administrative/professional experience with data related responsibilities (e.g. research, statistics, registry) or clinical research experience, OR + Graduate of an accredited allied health certificate program and two years of administrative/professional experience with data related responsibilities (e.g. research, statistics, registry) or clinical research experience, OR + Two (2) years of direct clinical research data entry experience OR three years of equivalent administrative/professional experience working with data or medical information to include duties such as data collection, management and verification. This facility is an equal opportunity employer and complies with federal, state and local anti-discrimination laws, regulations and ordinances. The salary range reflects the anticipated base pay range for this position. Individual compensation is determined based on skills, experience and other relevant factors within this pay range. The minimums and maximums for each position may vary based on geographical location. **Category:** Research **Organization:** AdventHealth Orlando **Schedule:** Full-time **Shift:** 1 - Day **Req ID:** 25006922 We are an equal opportunity employer and do not tolerate discrimination based on race, color, creed, religion, national origin, sex, marital status, age or disability/handicap with respect to recruitment, selection, placement, promotion, wages, benefits and other terms and conditions of employment.