Back to jobs
I

Clinical Data Manager

Spring House, PA, United StatesPosted 113 months ago
ContractonsiteMid-Senior Level

Job Description

PRINCIPAL RESPONSIBILITIES:

List most complex or difficult parts of job first. Describe scope of responsibilities.

  • Work with Study Teams and partners during study build process to create/maintain the following in CTMS:
  • Study, Country, Site, Contacts, and Institution records
  • Create and set up templates such as Health Authority, IRB/IEC, Financial Disclosure, Subject Visit, Visit/Trip Report, etc.
  • Update system dropdown values
  • Create/Update assignments, configurations, properties, attributes, triggers, and parameters in the system.
  • User administration
  • Import/Export templates
  • Add Payees and study triggers
  • Visit Schedules
  • Subject deviations/central findings
  • Any other general study build activities
  • Troubleshoot integration errors between CTMS and other applications
  • Provide Study build activities for Grants Manager
  • Create study
  • Upload templates
  • Create/Add sites
  • User administration (send invitations)
  • Any other general study build activities
  • Assist with UAT activities
  • Provide general business support for CTMS and Grants Manager applications
  • Create/Generate reports
  • Run SQL queries
  • Support Ticket generation/creation and maintenance (tracking of issues/requests)
  • Create/Update reference and training materials/documentation

PRINCIPAL RELATIONSHIPS:

Reports to Manager, Clinical Trial Management Business Support

Internal interfaces: Study Teams, Champions, Transition Agents, Other support team members, IT.

External interfaces: External vendors as necessary (e.g., flexible resource, Medidata vendor).

EDUCATION AND EXPERIENCE REQUIREMENTS:

  • Include any degrees or certifications which are required and/or desirable.
  • University/college degree is required; preferred in health, computer science, business, engineering, or information technology
  • Preferred prior experience with Medidata CTMS and/or Siebel CTMS or other Clinical Trial Management systems.
  • Knowledge of the Clinical Trial Management process
  • Oracle SQL experience is preferred but not required
  • 3 - 5 years of professional experience.

Kind Regards,

Sasha Sharma

Clinical Recruiter

Integrated Resources, Inc.

IT Life Sciences Allied Healthcare CRO

DIRECT # - 732-662-7964

See Your Match Score

Sign up and Renata will show you how this job matches your skills and experience.

Get Started Free
Clinical Data Manager at Integrated Resources INC | Renata