Clinical Data Manager

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.

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