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Data Coordinator
Data Coordinatorswipejobs • Brentwood, TN, United States
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Data Coordinator

Data Coordinator

swipejobs • Brentwood, TN, United States
[job_card.30_days_ago]
[job_preview.job_type]
  • [job_card.full_time]
  • [job_card.part_time]
[job_card.job_description]

Overview

Data Coordinator role at swipejobs. This posting describes responsibilities, qualifications, compensation, and work expectations.

Base pay range

$24.00 / hr - $24.00 / hr

Job Description

Are you a detail-oriented and organized Data Coordinator located near Brentwood, TN? Do you have at least 1 year of experience in healthcare, research, or other science related field? Apply today to join a team where your growth, well-being, and success are our top priority!

Details

  • $24 per hour pay rate
  • Full Time
  • Contract
  • Onsite in Brentwood, TN
  • Schedule : 8am - 4pm M-F

What's in it for you?

  • Health, Dental, Vision insurance offered
  • 401k options
  • Work with a great team

    • Qualifications

  • High School Diploma - Required
  • Bachelor's Degree - Preferred
  • 1+ years of experience in healthcare, research, or other science related field - Required
  • Knowledge of scientific, medical, and regulatory terms
  • Understanding of clinical research process
  • Knowledge of GCP and GMP
  • Professional writing and communication skills
  • Organizational and prioritization skills
  • Computer skills with ability to use clinical trial databases, electronic data capture, MS Access or Excel
  • High computer literacy and ability to learn new software

    • 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
  • Support Clinical Project Manager to meet industry trial data deadlines
  • Obtain source documentation for patients enrolled into clinical trials
  • 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 efficiency and quality
  • 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 perform other related work as needed
  • Assess adherence to HRI SOPs, Good Clinical Practice (GCP), and ICH regulations and guidelines

    • Seniority level

  • Entry level

    • Employment type

  • Part-time

    • Job function

  • Information Technology

    • Industries

  • Software Development

    • Referrals increase your chances of interviewing at swipejobs.

    Brentwood, TN

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