Submissions Manager, Global PV Operations at Otsuka Pharmaceutical

Posted in Other 7 days ago.

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Location: Princeton, New Jersey





Job Description:
As a member of the Global Pharmacovigilance Department, the Submissions Manager, Global PV Operations is responsible for managing the day to day operations of the Global Submissions Team. This team is responsible for the reporting of adverse event data in compliance with applicable global regulations. The Submissions Manager Global PV Operations will ensure responsibility for all the reports and submissions for the company's medicinal and device products covering pre and post marketing activities. The role holder will be a dedicated manager who will be running the reporting system of the GPV department which includes managing the safety report schedule, resources needed and reporting rules within the global safety database. With the responsibility for maintaining compliant and core safety documents, planning all updates scheduling and carrying out all submissions within applicable regulatory timelines. The Submissions Manager Global PV Operations will participate in the set-up and development of monitoring tools and maintenance of submissions workflow within the global safety database to meet global regulatory reporting requirements. In addition, the Submissions Manager Global PV Operations will assist with the reconciliation of submission dates, site audit requests, and health authority responses. The Submissions Manager Global PV Operations will assist in special projects as assigned by senior leadership. Must maintain continuous knowledge and expertise of local and global requirements for safety reporting. Must also maintain a thorough knowledge and understanding of internal and collaboration partner reporting rules.

Additional Responsibilities Include:
  • Manages the internal submissions process for all destinations including regulatory bodies, collaborating companies and internal departments.
  • Manage the submission process of SUSARs to IRB's, EC's and investigators.
  • Tracks and monitors all ICSR timelines to ensure that submissions to regulatory agencies, collaborating companies, and contract research organizations (CROs) are compliant with regulatory requirements.
  • Identifies/anticipates roadblocks and helps identify solutions to support the scheduling and timelines of major regulatory submissions.
  • Ensures the accuracy and completeness of electronic and hard copy regulatory submissions.
  • Provides support during interactions with regulatory agencies reviewing submission content.
  • Contributes to process improvement initiatives across the organization.
  • Assists with other regulatory activities and special projects as required.
  • Support the Manager PV Operations (Global ICSR Quality and Analytics) and team, escalating and investigating safety and non-compliance issues. In conjunction with the Manager PV Operations (Global ICSR Quality and Analytics) and team, escalating and investigating safety and non-compliance issues. In conjunction with the Manager PV Operations (Global ICSR Quality and Analytics) identify root causes for late ICSR submissions and implementation of appropriate corrective actions.
  • Actively manage the safety report scheduling, resources and timelines.
  • Review pharmacovigilance agreements and safety management plans.
  • Participate in the configuration of the safety database for products and studies.
  • Track and maintain compliance with regulatory timelines and submission requirements.
  • Work closely with the safety surveillance and case processing teams to achieve submission timelines
  • Assess impact of new regulations on the safety database reporting rules and oversees updates as appropriate
  • Participate in cross-functional meetings as the submissions lead.
  • Responsible for organizing and tracking safety information requests and ICSR related health authority responses
  • Maintaining a strong GPVP & GCP knowledge.
  • Generate and use established reports to monitor daily case workload and reports due, working with team members to identify potential bottle necks or resource gaps and coordinate work plans accordingly
  • Generate and use established reports to monitor reports worklist and additional worklist as needed.
  • Participate in the set-up and maintenance of adverse event workflow processes, department policies, and standard operating procedures
  • Follow company processes and guidelines for case management and closure activities, and adhere to company templates and guidelines for documentation and communications
  • Ensure compliance with corporate and departmental standard operating procedures
  • Contributes to development of standardized practices, procedures, metrics and measures productivity and performance within PV Operations.
  • Manage department staff
  • May provide support and back-up to the Global PV workflow Associate
  • Perform other activities as directed by senior leadership within Global Pharmacovigilance Provide management and oversight of E2B warnings and failures


Knowledge
  • Must have sufficient experience and a demonstrated thorough knowledge and understanding of global safety reporting regulations and guidelines including the FDA, ICH, & EU Regulations and Requirements for Pharmacovigilance
  • Knowledge of the ARGUS Safety Database
  • Experience of case management and safety report submissions metrics
  • Knowledge and prior experience in case processing*
  • Knowledge of the interworking's of Global Pharmacovigilance organization is desired
  • Experience with managing vendors, partners, and/or CRO's preferred Skills
  • Excellent technical skills, including the ability to comprehend and integrate scientific data from a variety of sources.
  • Strong communication and writing skills.
  • Strong computer skills with demonstrated experience in working with the Microsoft suite of programs (Word, Excel, PowerPoint, and Outlook).
  • Knows how/when to apply organizational policy or regulatory procedures to a variety of situations
  • Ability to work under pressure in order to meet tight timelines
  • Able to work effectively in a matrix environment
  • Strong attention to detail along with the ability to problem solve
  • The ability to provide direction to a team, and to influence peers and team members appropriately preferred
  • Excellent project management skills with the ability to align internal and external resources
  • Demonstrated competence in obtaining, analyzing, disseminating, and reporting safety information in compliance with global regulations


Education and Related Experience
  • Degree preferred to be in Bachelor of Science or related healthcare degree however may be waived for relevant experience
  • Minimum of 5 years drug safety experience required Demonstrated proficiency in safety database functionality
  • Global Drug Safety Case processing experience
  • Safety experience is defined as actual experience processing AE/SAE reports, generating narratives, queries, working within safety databases, and experience with regulatory submissions.
  • Relevant experience includes experience in the pharmaceutical, biotechnology, or CRO industry, partly in related areas such as Medical Affairs, Clinical Data Entry and Clinical Data Management, Clinical Monitor, Regulatory Affairs, or Quality Assurance


Disclaimer: This job description is intended to describe the general nature and level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. Otsuka reserves the right to amend and change responsibilities to meet business and organizational needs as necessary.Otsuka is an equal opportunity employer. All qualified applicants are encouraged to apply and will receive consideration for employment without regard to their protected veteran or disabled status, or any protected status.

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