Recent Searches

You haven't searched anything yet.

1 251069 - CTMS Program Analyst- Full time- Clinical Trials Job in Detroit, MI

SET JOB ALERT
Details...
251069 - CTMS Program Analyst- Full time- Clinical Trials
$82k-101k (estimate)
Full Time 1 Month Ago
Save

sadSorry! This job is no longer available. Please explore similar jobs listed on the left.

CTMS Program Analyst- Full time- Clinical Trials - Henry Ford Health System Careers is Hiring a 251069 - CTMS Program Analyst- Full time- Clinical Trials Near Detroit, MI

GENERAL SUMMARY:

  • Under general supervision of the Data Operations Manager for OnCore Support, the Clinical Trials Management System (CTMS) Program Analyst is responsible for serving as the first line of technical support for CTMS electronic systems at Henry Ford Health.
  • These include Advarra's OnCore and eRegulatory, as well as any related interfaces with additional systems, and any future systems deployed to support the research mission at Henry Ford Health.
  • Responsible for assisting with the setup, build, activation and ongoing support of all trial types (federally funded, industry-sponsored, and investigator initiated human subject research).
  • Works directly with research departments and provides reporting, additional training, and auditing of each system to ensure Henry Ford Health minimum data requirements in OnCore and eRegulatory are being achieved.
  • Provides support with system implementation, creating user accounts, managing calendar and budget build requests, and research department calendar queries.
  • This position will be a key member of the OnCore support team and will support operations, management of research departments within the Advarra systems, subscription utilization, and regulatory compliance.
  • Utilizes technical analytical skills to seek out, research and evaluate a variety of solutions to provide research personnel with high quality, efficient workflows and data that promote efficiency and enterprise-wide standardization. 

EDUCATION/EXPERIENCE REQUIRED:

  • Bachelor's Degree in a scientific discipline.
  • Three (3) years of clinical trials experience.
  • Coordinator experience preferred.
  • Previous application and database support experience strong preferred.
  • Experience with MS Excel/Access/Word/PowerPoint/Outlook/Visio preferred.
  • SQL experience preferred.
  • Able to communicate in a professional, courteous, and effective manner (written and verbal).
  • Able to problem solve and trouble shoot application matters.
  • Able to develop and maintain strong working relationships with key clients, vendors and staff.
  • Able to lead and/or participate in task groups to define, develop, document, communicate, and implement process improvements and initiatives.
  • Understanding of desktop computer hardware and software configurations on a range of computing platforms including desktops, laptops, tablets, etc.
  • Familiarity with standard concepts, practices, and procedures as they relate to operating systems, and networking.
  • CERTIFICATIONS/LICENSURES REQUIRED: CCRP or ACRP Certification preferred.

Job Summary

JOB TYPE

Full Time

SALARY

$82k-101k (estimate)

POST DATE

03/11/2023

EXPIRATION DATE

06/13/2023

Show more