Unfortunately, this job posting is expired.
Don't worry, we can still help! Below, please find related information to help you with your job search.
Some similar recruitments
Associate Research Strategy & Programs Specialist
Recruited by Vanderbilt University Medical Center 8 months ago Address Nashville, TN, United States
Clinical Research Associate Jobs
Recruited by Sarah Cannon 9 months ago Address Nashville, TN, United States
Research Data Analyst Jobs
Recruited by Vanderbilt University Medical Center 9 months ago Address Nashville, TN, United States
Sr. Research Strategy & Program Specialist **Remote Available**
Recruited by Vanderbilt University Medical Center 9 months ago Address Nashville, TN, United States
Clinical Data Analyst - Wfh
Recruited by Sarah Cannon 10 months ago Address Tennessee, United States
Associate Research Strategy & Program Specialist **Remote Available**
Recruited by Vanderbilt University Medical Center 1 year ago Address Nashville, TN, United States

Clinical Research Data Specialist

Company

Medasource

Address Nashville, TN, United States
Employment type FULL_TIME
Salary
Category Research Services,Hospitals and Health Care
Expires 2023-10-13
Posted at 7 months ago
Job Description

Contract Duration: 6 Month Contract to hire

Location: Remote. with onsite travel once a month

: Our client, an academic medical center based out of Nashville Tennessee is looking to bring on a skilled Clinical Research Data Specialist to monitor data functions and the conduct of research protocols. This individual will be joining one of three teams focused on either Liquid Tumors, Cellular Therapy, or GI studies.


Responsibilities:

  • Ensure data is correctly input into the system and quality of clinical research is maintained
  • Attend staff meetings with disease team and physicians to share what is outstanding, where we are having issues, and what adjustments need to be made.
  • Utilizes Query Trackers to reconcile, clarify, and complete data issues
  • Direct others with interpretations of rules and regulations
  • Effectively apply tools to address specific issues
  • Prepared for and participates in internal and external audits and action plans needed from these results.

Qualifications:

  • 2-3 years of experience in clinical research data entry
  • Bachelor's degree in Research or related field
  • Prior oncology knowledge
  • Strong organization and communication skills