Clinical Research Data Coordinator at HCA Florida Largo Hospital
Largo, FL 33770, USA -
Full Time


Start Date

Immediate

Expiry Date

12 Oct, 25

Salary

0.0

Posted On

13 Jul, 25

Experience

1 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Research

Industry

Hospital/Health Care

Description

INTRODUCTION

Are you passionate about the patient experience? At HCA Healthcare, we are committed to caring for patients with purpose and integrity. We care like family! Jump-start your career as a Clinical Research Data Coordinator today with HCA Florida Largo Hospital.

JOB SUMMARY AND QUALIFICATIONS

The Data Coordinator is responsible for EMR data abstraction, EDC data capture, assisting with AE/SAE reporting and study queries. Ensures all activities are conducted according to company SOPs, and all applicable GCP and ICH regulations and guidelines.

Education & Experience:

  • High School Diploma Required
  • Bachelor’s Degree Preferred
  • 1+ years of experience in healthcare, research, or other science related field Require

How To Apply:

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Responsibilities
  • Support data entry activities to meet study data needs and deadlines
  • Data abstraction from diverse sources
  • Obtain source documentation for patients enrolled into clinical trials and data registry
  • Maintain Data Registry as directed
  • Assist with Data validation, conflict resolution and quality assurance
  • Supports Clinical Project Manager to meet industry trial data deadlines
  • Obtain source documentation for patients enrolled into clinical trial
  • Assist Clinical Project Manager with case report form completion
  • Assist Clinical Project Manager with query resolution
  • Assist in SAE reporting and tracking
  • Create and maintain patient visit tracking spreadsheets
  • Maintain and archive study documents
  • Meet with clinical study sponsor representatives as requested
  • Develop and maintain file management and collaboration systems
  • Maintain calendar
  • Initiate improvements, tools, processes, and forms to enhance the efficiency and quality of work
  • Attend meetings as assigned and report on actions
  • Participate in educational activities and programs
  • Maintain strictest confidentiality
  • Work closely and effectively with all other department colleagues
  • Assist other staff as requested and performing other related work as needed.
  • Throughout the conduct of the clinical trial assesses adherence to HRI SOPS, Good Clinical Practice (GCP) and ICH regulations and guidelines
  • All other duties as assigned

Education & Experience:

  • High School Diploma Required
  • Bachelor’s Degree Preferred
  • 1+ years of experience in healthcare, research, or other science related field Required

“The great hospitals will always put the patient and the patient’s family first, and the really great institutions will provide care with warmth, compassion, and dignity for the individual."- Dr. Thomas Frist, Sr.
HCA Healthcare Co-Founder
If you are looking for an opportunity that provides satisfaction and personal growth, we encourage you to apply for our Clinical Research Data Coordinator opening. We promptly review all applications. Highly qualified candidates will be contacted for interviews. Unlock the possibilities and apply today!
We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status

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