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
• Debt-free Education* (Certifications and Degrees without out-of-pocket tuition expense)

THE EXPERTISE AND EXPERIENCES YOU’LL NEED TO SUCCEED:

• Bachelors degree in healthcare related field, data processing or related field, OR
• Associate degree in health science, or related field, and one (1) 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 (2) 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 (3) 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: 25030132
  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.

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.