Primary Skill: Support an initiative to improve the audit readiness of our Pharmacovigilance (PV) IT systems and staff. This resource will coordinate the assessment document findings track remediation and ensure deliverables are organized complete and inspection-ready.
Secondary Skill: Strong project management communication writing and organization skills. High attention to detail follow-through and ownership. Ability to manage multiple stakeholders priorities and deadlines independently. Proficiency with Microsoft Office Teams SharePoint and project tracking tools.
Responsibilities Coordinate PV IT audit readiness assessment and remediation activities. Manage meetings agendas notes decisions and action items. Document gaps risks remediation plans evidence and follow-ups. Maintain trackers status reports and organized project documentation. Engage IT Quality Compliance PV business stakeholders and system owners. Track issues dependencies and open actions through closure. Identify opportunities to streamline current processes and recommend practical improvements to strengthen audit readiness.
Required Skills Strong project management communication writing and organization skills. High attention to detail follow-through and ownership. Ability to manage multiple stakeholders priorities and deadlines independently. Proficiency with Microsoft Office Teams SharePoint and project tracking tools.
Preferred Experience GxP-regulated environments SDLC methodology validation documentation or audit readiness. Compliance assessments remediation tracking or inspection readiness support. Pharmacovigilance quality compliance or R&D technology experience; prior auditing is ideal but not required.
Job Title: IT Audit Support Job Location: Raritan NJ (Onsite from day one) Job Duration: 12 months Minimum years of experience required: 5 years Type of Hire: w2 contract JOB DETAILS: Primary Skill: Support an initiative to improve the audit readiness of our Pharmacovigilance (PV) IT syst...
Job Title: IT Audit Support
Job Location: Raritan NJ (Onsite from day one)
Job Duration: 12 months
Minimum years of experience required: 5 years
Type of Hire: w2 contract
JOB DETAILS:
Primary Skill: Support an initiative to improve the audit readiness of our Pharmacovigilance (PV) IT systems and staff. This resource will coordinate the assessment document findings track remediation and ensure deliverables are organized complete and inspection-ready.
Secondary Skill: Strong project management communication writing and organization skills. High attention to detail follow-through and ownership. Ability to manage multiple stakeholders priorities and deadlines independently. Proficiency with Microsoft Office Teams SharePoint and project tracking tools.
Responsibilities Coordinate PV IT audit readiness assessment and remediation activities. Manage meetings agendas notes decisions and action items. Document gaps risks remediation plans evidence and follow-ups. Maintain trackers status reports and organized project documentation. Engage IT Quality Compliance PV business stakeholders and system owners. Track issues dependencies and open actions through closure. Identify opportunities to streamline current processes and recommend practical improvements to strengthen audit readiness.
Required Skills Strong project management communication writing and organization skills. High attention to detail follow-through and ownership. Ability to manage multiple stakeholders priorities and deadlines independently. Proficiency with Microsoft Office Teams SharePoint and project tracking tools.
Preferred Experience GxP-regulated environments SDLC methodology validation documentation or audit readiness. Compliance assessments remediation tracking or inspection readiness support. Pharmacovigilance quality compliance or R&D technology experience; prior auditing is ideal but not required.