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Open nowPosted 3534 days ago

Clinical Data Manager

Integrated Resources INC2,463 open roles

Where
Spring House, PA, United States
Work mode
On site
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Your applicationOpen nowClinical Data ManagerIntegrated Resources INC · Spring House, PA, United States

  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on Integrated Resources INC's own form.

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The clock on this job

Early applications get read.

11.3% of postings close within 7 days. Measured by our own scanner across the market. Integrated Resources INC postings stay open a median of 15 days.

Share of postings closed within
  1. 2.0%1 day
  2. 4.2%3 days
  3. 11.3%7 days
  4. 17.6%14 days
  5. 34.3%30 days
  6. 43.5%60 days
This job: posted 3534 days ago

Integrated Resources INC median: 15 days open

The posting

Company Description

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.

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).

Qualifications

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.

Additional Information

Kind Regards,

Sasha Sharma

Clinical Recruiter

Integrated Resources, Inc.

IT Life Sciences Allied Healthcare CRO

DIRECT # - 732-662-7964

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