SCRI-RESEARCH DATA COORDINATOR

Job ID: 45579
Positions Location: Lansing, MI Job Description General Purpose of Job: Work Description:

Positions Location: Lansing, MI

Job Description

General Purpose of Job:

Work closely with Clinical Research Coordinators (CRCs) in entering study data into electronic case report forms in compliance with all the policies, procedures, regulations and requirements of Good Clinical Practice (GCP), Institutional Review Boards (IRB), research sponsors and other regulatory agencies (ie FDA) and specific to each clinical trial.

Essential Duties:

This job description is intended to cover the minimum essential duties assigned on a regular basis. Associates may be asked to perform additional duties as assigned by their leader. Leadership has the right to alter or modify the duties of the position.

• Prepare for and attend study initiation
• Complete any study specific Case Report Forms (CRF) training and any other requirements for study data management
• Develop worksheets to gather necessary and relevant medical information
• Complete CRFs accurately and within the study timeframe
• Assist CRC in responding to all queries within the study timeframe
• Work with CRC and Study Monitor on CRF questions at site visits
• Assist Regulatory coordinators with data needed for IRB submissions
• Work with CRC on obtaining any missing data and outside medical records
• Work with CRC to resolve any open findings from the Study Monitor
• Work with sponsor & CRC to prepare study for final closeout and archiving of records
• Participate in Research Quality Assurance program to ensure accurate study records
• Serve as liaison between patients, study staff and physicians to answer questions and address concerns
• Facilitate and participate in on-going communication and follow up with customers of Research department
• Track office supply inventory and reorder as needed
• Communicate with Billing department regarding study patient procedures
• Answer department phone calls and route accordingly
• Assist study team with other activities as needed

Job Requirements

General Requirements

• None

Work Experience

• Minimum three years clinical research or medical office

Education

• High School Diploma or GED

Specialized Knowledge and Skills

Required: • Communication and organizational skills • Computer skills (Word, Outlook, Excel) • Medical terminology • Ability to learn research tasks within training period. • Obtain and maintain certification in good clinical practice and hazardous material shipment. Preferred: • Associates Degree • Regulatory Coordinator, research staff or IRB experience

Sparrow Health System is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected Veteran status.

Job Family
Administrative/Clerical Requirements: