Posted to MedZilla on 12/14/2019


United States, RIM Data Analyst SS_EF_13638-MZ


ProClinical is recruiting for the position of an RIM Data Analyst on a contract basis. The ideal candidate will perform comprehensive data analysis to aid in the development of an integrated regulatory information technology solution that will facilitate global tracking, business workflow, reporting and analysis of critical Regulatory information and work output, including product registration, health authority interaction, document/content management, communications, and business analytics. RIM will serve as the lifeblood to the regulatory lifecycle management of all products  across multiple Medical Devices business units globally.


  • Take complete inventory of all regulatory information artifacts from specified regulatory affairs business units (and relevant non-regulatory information sources).
  • Support development of accelerated plan for data maintenance and analysis phase and coordinate with relevant teams.
  • Execute data maintenance plan.
  • Establish strong working relationships with key data stakeholders.
  • Identify critical gaps and/or impediments to effectively achieving goals.
  • Identify/escalate critical issues in a timely manner.
  • Provide necessary input to project dashboards/progress checks at regular intervals.

Skills And Requirements

  • BA or equivalent and 2+ years relevant experience.
  • Relevant data management experience/expertise.
  • Understanding of regulatory business process preferred.
  • Ability to rapidly gather and process information from key business partners to understand the various regulatory business function and supporting data artifacts, including sources of data, quality of data and understanding how data flows in/out of function.
  • Ability to understand cross-enterprise data flow and systems.
  • Working knowledge of accepted and emerging healthcare information standards.
  • Fosters excellent cross-functional communications and works effectively across team to achieve business objectives.
  • Excellent communication skills, ability to establish positive working relationships and gain trust of business partners.
  • Strong analytical and organizational skills with the ability to work cross-functionally.
  • Preferred experience working within health care regulatory environment such as medical devices, pharmaceuticals or consumer products.
  • Ability work collaboratively in a highly matrixed environment.
  • A strong results-orientation and sense of urgency whilst demonstrating proficiency and success in prioritizing and handling multiple tasks simultaneously.
  • Strategic thinking and ability to partner with internal stakeholders at multiple levels of the organization.
  • Ability to achieve results under demanding time constraints with expansive and changing priorities.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please call Eleni Farrell on (+1) 2679830134 or upload your resume on our website -

A full job description is available on request.

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Please visit our website at


* If a direct employer requests that you go to their web site and complete your application there in order to be
  considered, please do so. Applications for all positions are subject to each employer's specific requirements.