Program Coordinator, Regulatory Information Manager

Integrated Resources INC

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Cambridge, MA, us on site Until 8/21/2026 H-1B sponsor history First posted February 23, 2026 Last posted February 23, 2026
Job 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.

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. 

  • 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.

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)

About this role

Summary

Coordinate regulatory data review, facilitate process overhaul, support RIM platform upgrade.

Job title

Program Coordinator, Regulatory Information Manager

Experience level

Industry

healthcare

Location requirements

On-site in Cambridge, MA, no remote work specified.

Salary

Not specified

Visa sponsorship

H-1B sponsor history

Management role

No

Skills & keywords

Required skills

regulatory dataregulatory processesXEVMPD

Preferred skills

None specified

Specializations

regulatory dataEMAIDMPXEVMPDregulatory processes
Locations

Structured locations inferred from the posting.

Cambridge, MA, USA

On-site City