Job Title :Regulatory Submission Project Management Associate
Location: Des Plaines IL 60018
Duration: 08 Months 

The Submission Project Management Associate is a Regulatory Operations team member responsible for working with the product team members to create and deliver on the regulatory submission project plan deliverables and ensure that responsible parties are meeting expectations. 
This individual must be able to understand the submission process, its requirements, timelines and assist others to resolve issues that could negatively affect getting work completed. 
The candidate will provide transparency to project risks and issues to the team, develop/execute mitigation plans to eliminate those issues/risks for deliverables on the critical path and escalate as appropriate to upper management. As an individual contributor, the function of the Submission Project Management Associate is to provide support for the regulatory department to ensure efficient and compliant business processes and environment. 
The individual may execute tasks and exercise influence generally at the middle management level. 
The individual may assist in the registration of products by preparing and submitting documentation needed for registration worldwide. 
Regulatory Knowledge / Skills 
Regulatory history, guidelines, policies, standards, practices, requirements and precedents 
Submission/registration types and requirements 
Domestic and international regulatory guidelines, policies and regulations 
Ethical guidelines of the regulatory profession, clinical research and regulatory process. 
 
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $ 44.00/daily.