NTRO RESEARCH COORDINATOR I

Summary Position Highlights

Primary focus is participant recruitment, inclusive of specimen and data collection.
Captures responsibilities such as specimen and data collection, study coordination, and administrative tasks.
Works under general supervision from NTRO supervisor or manager and Principal Investigator.
First level of a research coordinator career path.

Responsibilities

• Screen, identify eligibility, and consent research participants.
  Document the consent process pursuant to regulatory and Moffitt guidelines.
  Enter data and information into Redcap, Powerchart, OnCore, or sponsor-specific EDC.
  Ensure data quality and protocol adherence.
  Ensure proper specimen collection at required time points; may include phlebotomy.
  Conduct surveys and/or interviews for applicable studies.
  Set up offsite recruitment activities and materials when needed.
  Update protocols with PI guidance for Regulatory submissions.
  Document deviations and communicate with stakeholders.
  Communicate standardized information with Regulatory Specialist and shared resources.
  May contribute to publications, abstracts, presentations and manuscripts.

Credentials & Qualifications

• Associate’s degree in field relating to public health, psychology, biological sciences or relevant field.
  General knowledge of medical terminology and general computer skills (Microsoft Office Suite).
• Ability to plan, organize and coordinate work assignments.
  Excellent verbal and written communication and critical thinking skills with ability to adapt quickly.
  Ability to build stable working relationships.

Preferred Skills

• Knowledge of EMR systems, OnCore, RedCAP, and applicable certifications (BLS/CPR, Phlebotomy, Spanish Language Fluency, Certified Nutrition Coach, Personal Trainer certifications).