Program Coordinator, Regulatory Information Manager

Integrated Resources IncVerified source: this listing comes from the employer's official hiring system or a verified company · Cambridge, United States · Onsite
Listed via SmartRecruiters
Posted Jul 11, 2017 · Apply by Nov 6
Recently checked

Last checked active on Aug 8, 2026.

Position Overview

Compensation: Not disclosed
Position: Senior
Type: Job
Employment: Contractor
Practice Area: Regulatory Compliance
Remote: No
Deadline: Nov 6, 2026

Job Description

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

This role will be coordinating work across 2 major initiatives. One set of work will be tied to approach to IDMP (Identification of Medicinal Products), and the activities specifically tied to the introduction of the European Medical Agency (EMA) introduction of underlying infrastructure services, called SPOR. This near term activity will be engaging across groups, primarily within R&D, and largely regulatory to complete the data review of the provided controlled vocabularies for accuracy as industry, and from a  perspective, as well as managing the feedback on changes required back to EMA services. 

Qualifications

  • While IDMP in depth is not required, there is a preference for someone who has sufficient context, thus an individual familiar with regulatory data and processes, and someone who is familiar with current XEVMPD (EMA Article 57) would be the best fit. 
  • The other set of work is in pre-work developing the implementation plan for upgrading our Regulatory Information Management (RIM) platform

Note, the focus for this role is not the system component; rather, it is with the organization, facilitation and work related to the overhaul of business processes that are being re-introduced within the context of Regulatory business practices which will enable  to move forward with a return to a more standard deployment of our RIM system. Thus, someone who is familiar with regulatory data and processes is the primary requirement. Depth/experience is agnostic of specific RIM systems, though a level of familiarity with the RIM industry landscape and capabilities is a plus.

Additional Information

Thanks!!

With Regards,
Sasha Sharma
Clinical Recruiter
Integrated Resources, Inc
IT REHAB CLINICAL NURSING
Direct: 732-662-7964 | (W) 732-549-2030 x 219

Inc. 5000 – 2007-2015 (9 Years in a row)

Practice Area

Position

Senior

Required Skills

Regulatory Compliance, Regulatory Affairs, Risk Management

Industry

Staffing

Application Deadline

November 6, 2026

Employment Type

Contractor

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