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Worldwide Clinical Trials

PRN Data Coordinator

Worldwide Clinical Trials

. Review study protocols for assigned studies .

Posted 9/23/2026part-timeRemote • Texas • United StatesMid-LevelSenior💰 $14 - $29 per hourWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates strong attention to detail and excellent communication skills while ensuring accurate data entry and adherence to Good Clinical Practices in clinical research. Capable of effectively tracking study protocols and managing documentation under supervision.

Highest-signal resume keywords
Excellent Written Communication SkillsExcellent Oral Communication SkillsAttention To DetailKnowledge Of Good Clinical PracticesBachelor’s Degree In Life Sciences

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Data EntryCase Report Form ManagementStudy Protocol ReviewRecord ReconciliationClinical Research Process Knowledge
Soft Skills
Interpersonal SkillsAbility To Follow Instructions
Tools & Technologies
Electronic Case Report FormsBasic Computer Applications
Industry Keywords
Clinical ResearchGood Clinical PracticesPhase I Clinical Environment

About the role

Key responsibilities & impact
  • Review study protocols for assigned studies
  • Ensure source-document data is accurately reflected on electronic or paper Case Report Forms
  • Track source documents filed into subject folders
  • Assist with reconciliation of study records for archive
  • Identify and report problems or potential problems to the supervisor
  • Request, schedule, and attend required training
  • Work under the general supervision and guidance of the Senior Manager, Study Conduct

Requirements

What you’ll need
  • Excellent written and oral communication skills
  • Ability to understand complex written and oral instructions
  • Basic computer knowledge and applications for business correspondence and electronic Case Report Form data entry
  • Strong interpersonal skills
  • Excellent attention to detail
  • Some knowledge of the clinical research process, including Good Clinical Practices
  • Bachelor’s degree or associate degree, preferably in Life Sciences or Health, and/or experience in a phase I clinical environment
  • Preferred: Experience or class work in the health field

Benefits

Comp & perks
  • Competitive benefits package depending on location
  • Inclusive and equitable workplace
  • Transparent compensation and pay equity