
Data Coordinator
- Grand Rapids, MI
- $30.00-35.00 per hour
- Contract
- Full-time
- Review and update spreadsheets with information from current and older studies.
- Gather detailed information from various sources, including Clinical Research Coordinators (CRCs).
- Ensure all data is accurately listed for financial clean-up and CTMS integration.
- Enter active study information into the CTMS, collaborating with internal partners for accuracy.
- Assist in the implementation of the CTMS, potentially providing input on tool layout, user interface, and training documents.
- Create processes related to CTMS implementation.
- Optionally transition into a Clinical Research Coordinator role based on interest and experience.
- Experience in data management and clinical data handling.
- Familiarity with Clinical Trial Management Systems, preferably Oncore.
- Proven ability to work independently and complete projects autonomously.
- Experience working with clinical data for investigational drug studies.
- Experience in oncology and with Oncore is beneficial.
- Motivated and self-directed work ethic.
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:
- Medical, dental & vision
- Critical Illness, Accident, and Hospital
- 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
- Life Insurance (Voluntary Life & AD&D for the employee and dependents)
- Short and long-term disability
- Health Spending Account (HSA)
- Transportation benefits
- Employee Assistance Program
- Time Off/Leave (PTO, Vacation or Sick Leave)