PV Operations Associate

1 month ago

American Canyon, United States MSI Pharma Full time

MSI Pharma are working with a globally recognised pharma company to help source a PV Operations Associate. The ideal candidate will provide operational support to the US Patient Safety Clinical and Vendor Oversight teams to ensure proper performance of baseline PV compliance-based responsibilities. This is done through the implementation and regulation of global processes, local legislation, case investigation, and study management. Responsibilities are performed under the direction of the PV Operations Manager. Key Accountabilities: ·Perform Individual Case Safety Reports (ICSR) Activities · Performs Outbound Submission and Tracking (OST) for literature ICSRs and submits relevant documentation to the health authority · Ensure any non-compliance or late ICSR from programs are identified and ensure deviations are filed in accordance with global processes · Assists and collaborates with Global ICSR team to inform on US Affiliate ICSR compliance performance and risks · Performs daily workflow coordination and initial review of cases that are processed by our internal teams · Oversees the enrolment process and proper onboarding of GVP vendor · Assists in the tracking and investigation of case processing related metrics · Supports Late ICSR Investigation and Risk Mitigation Strategy · Ability to review the late case(s) to determine root cause analysis (RCA) and corrective action preventative action (CAPA) as needed · Provide regular ICSR compliance updates, highlight potential risks or trends and escalate issues to Team Leads and US PS Leadership Support implementation of CAPAs and business units where required on appropriate CAPA to any findings · Continuous review of ICSR compliance trends to inform risk mitigation strategy to avoid non-compliance for the US affiliate · Liaise and collaborate with vendor oversight teams to ensure external and internal stakeholder compliance · Supports all study management related activities · Responsible for oversight, triage, and tracking of incoming study document review request · Responsible for performing Case Transmission Verification (CTV) · Ensuring all US Medical Affairs (USMA) studies have been reviewed and assessed by PV Clinical Group · Partners with key stakeholders to ensure proper assessment and documentation of study related decisions · Escalates compliance risks or issues to management when identified · Assists in the tracking and investigation of metrics as required Supports MAP Operational related activities · Perform reconciliation related activities for Market Research Patient (MAP) support programs and responsible for tasks related to GoMAPto ensure continuous data integrity · Run operational metrics reports on a routine basis, identify required follow-ups, and work with the appropriate PV Operations member and/or Vendor Leads to ensure appropriate follow-up is completed · Responsible for executing Source Data QC (SDQC) of in-scope MAPs on a routine basis. This includes a) Communication with MAP vendors; b) management of vendor conducting SDQC, including appropriate QC; receiving, QC, and tracking data files · Ensure all MRP and PSP programs documentation (including Service Provider training, CTV, SDQC, contracts) are tracked in GoMAPensuring continuous data integrity · Assists in the tracking and investigation of metrics as required · Vendor Oversight for Outsourced Pharmacovigilance (PV) Activities · Understand the vendor management framework and translate the requirements into reporting deliverables · Support Lead on all operations performed, including training and the implementation of policies/procedures that ensure effective and compliant operations · Develops agendas and facilitates meetings as needed · Tracks status of metrics for outsourced activity and escalates to PV Operations Manager as required · Communicates closely with cross-functional teams within US PS to achieve the appropriate level of support to ensure oversight of outsourced activities · Leads or assists in the tracking, investigation and trending of case processing related metrics (e.g., late case investigation) including compliance-related issues set by the vendor management strategy team · PV Activity Classification and Promotional Review Material · Responsible for oversight of receipt and processing pharmacovigilance activity classification (PVAC) requests and/or safety-related queries. · Oversight and review of approved Promotional Review Committee (PRC) promotional marketing materials for proper oversight of market research programs and patient support programs (MAP). Education, Experience, and Other Requirements: · Minimum Bachelors degree (Preferred) · Degree in Life Science or related field (Preferred) · Demonstrates expertise in computer skills and database experience (i.e Microsoft Office Suite and Google Applications) (Preferred) · Proven ability to solve problems creatively · Familiarity with project management software tools, methodologies, and best practices · Excellent analytical skills and ability to translate complex data trends into actionable steps · Sound decision-making abilities as demonstrated by systematic gathering of information, appropriately assessing the complexity of issues, and prioritization of tasks in a timely manner within the scope of responsibility · Excellent communication skills, both written and verbal · Strong interpersonal skills and extremely resourceful #J-18808-Ljbffr

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