Senior Associate, Global Regulatory Systems & Process Mgmt
Location: Woodcliff Lake, NJ Duration: Fulltime
Sr Associate, Global Regulatory Systems & Process Management (GRSPM) will support GRSPM Head with management and coordination of systems and process within Global Regulatory Services and Operation team. This position will support Regulatory Systems initiatives contributing directly to the value of Global Regulatory Operations, and responsible for oversight and local level systems support for Global Regulatory Affairs. This position will also contribute to Process Excellence by evaluating, developing and providing input into existing and proposed processes. We are looking for a solution oriented person who ensures that deliverables and key submission targets are achieved according to the quality standards of client's standard operating procedures.
Ensure that Regulatory Information Systems are supported and managed according to business need, including, but not exclusively, FirstDoc, eCTD Express, Submission Viewer, Veeva Vault for Registrations and SharePoint. Processing and responding to change requests for systems or processes, additionally helpdesk type duties for the support of our business users.
Submission Management Support: this comprises business end user support of the Submission Management publishing tools and business processes for the GRO department.
Create and deliver Training to Business System Users: this will include identifying the training needs and these end users
Assume role as IT liaison. This will include managing system change request management and issue escalation.
Vendor Management: Working with vendors to manage change requests, Service Level Agreements and Compliance Management.
Engage with vendors and internal partners to drive future state of-the shelf software packages.
User Requirement Gathering and Dissemination, Process Design.
Service Request Management.
Gathering Business Feedback and Group Activity/Initiatives.
BS/BA with 3 years of regulatory submission related experience. Alternatively, 8+ years of hands on experience in regulatory submission/publishing without bachelor degree will be considered.
Previous experience in pharmaceutical industry an advantage
Experience with Systems, in particular in relation to Document Management, Regulatory Tracking and Publishing is beneficial
Knowledge of Regulatory and Submissions processes in the EU and US is also important, especially with knowledge for key Regulatory systems and report publishing
Strong verbal, written and interpersonal communication skills, especially relationship management, with ability to give/receive feedback and build consensus
Experience of mapping User Requirements to Functional Specifications especially in respect of process management an advantage
1st and 2nd line experience support around regulatory systems.
As an equal opportunity employer, ICONMA prides itself on creating an employment environment that supports and encourages the abilities of all persons regardless of race, color, gender, age, sexual orientation, citizenship, or disability.
* The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.