Regulatory Affairs Specialist

Details of the offer

Regulatory Affairs SpecialistApply locations: Cork, Carrigtwohill, Anngrove North SEO, Limerick, Limerick Raheen Business Park
Time Type: Full time
Posted on: Posted 2 Days Ago
Job Requisition ID: R532011
Work Flexibility: Hybrid
Key Areas of Responsibility: Identifies information sources and resources for local, regional, and global regulationsCollects, organizes, and maintains files on local, regional, and global regulatory intelligence and other related informationMonitors the regulatory environment (specific regulations, guidance, and other relevant information by product types, geography, etc.)Provides information used to evaluate proposed products for regulatory classification and jurisdictionResearches requirements (local, national, international), applicable guidance and standards, and options for regulatory submissions, approval pathways, and compliance activitiesAssists in the development of regulatory procedures and SOPsCollects and organizes information on requirements for regulatory, quality, preclinical, and clinical data to meet applicable regulationsOrganizes materials from preclinical and clinical studies for review and assists in the review processCompiles and organizes materials for pre-submission reports and communicationsAssists in the preparation of dossiers and pre-submission and submission packages for regulatory agenciesTracks the status of applications under regulatory review and provides updates to the regulatory teamMaintains logs of communication and outcomes with regulators and other relevant internal or external stakeholdersAssists in the scheduling of meetings with internal stakeholders and regulators and develops and organizes materials for these meetingsEducation / Work Experience: BS in Engineering, Science, or related degree; or MS in Regulatory Science0+ years experienceKnowledge / Competencies: Time management skills, writing, coordination, and execution of basic regulatory itemsCoordinate and support technical and scientific regulatory activitiesUnder supervision, performs work that is varied and that may be somewhat difficult in character, but usually involves limited responsibilitySome evaluation, originality, or ingenuity is requiredClearly conveys information to peers, supervisors, and other stakeholdersAssists in the preparation for meetings with regulatory agencies and other stakeholdersAssists in the preparation of briefings and other information documentsCommunicates information on regulatory requirements to other departments and business unitsComposes routine communications with regulators and other key stakeholdersCreates clarity and direction amid complexity and develops solutions for self, colleagues, and the organizationSeeks out diverse ideas, opinions, and insights, and applies them in the workplaceConnects and relates well with people who think and act differently than oneselfEmbraces scrutiny and accepts feedback as an opportunity to learn and improveTravel Percentage: None

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Nominal Salary: To be agreed

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