Associate

• Advise clients on corporate law matters, including mergers and acquisitions, corporate governance, directors' duties, shareholder arrangements, and general company law issues
• Take ownership of complex corporate matters and transactions
• Work directly with clients and partners to deliver practical, commercially focused outcomes
• Build and strengthen client relationships
• Contribute to business development initiatives
• Contribute to the growth of the Christchurch Corporate and Commercial practice
• Develop expertise across a diverse client base, from private businesses and founders to larger corporate organisations
• Work as part of a high-performing local and national team
• Take a lead role on significant transactions and advisory engagements
• Mentor and support junior team members

Senior Associate, Corporate and Commercial

• Provide support to other activities undertaken by the project team on behalf of the client and the company
• Perform ICSR management activities within agreed scope and timelines
• Process Individual Case Safety Reports from all sources in compliance with applicable regulations, company procedures and client-specific requirements
• Perform ICSR follow-up, SAE/SUSAR management, including unblinding, clinical trial reconciliation and protocol review
• Review Safety Management Plans
• Perform clinical and partner reconciliation
• Manage personal data protection activities
• Handle Product Quality Complaints and interact with Quality Assurance
• Interact with Medical Information teams
• Perform MedDRA and WHO coding
• Produce database outputs and reports, including monthly client reporting data
• Support workflow and resource management
• Support pharmacovigilance processes related to ICSR management for PrimeVigilance and clients
• Perform tasks assigned under SOPs to more junior positions when applicable
• Support the RA & PV Network Department as needed
• Act as LCPPV for the specified country and PRLS for the designated language, as agreed with the line manager

Senior PV Associate

• Manage customer onboarding requests through digital channels
• Guide clients from initial application through establishment of their first BNZ accounts
• Assist customers with application processes, inquiries, and follow-ups via digital platforms or telephone
• Conduct daily reviews of active applications and ensure adherence to follow-up schedules
• Fulfil service level agreements and support exceptional customer service
• Collaborate within the team to identify process improvements and foster a positive work environment

• Lead smaller programmes directly, manage major workstreams within nationally significant programmes, or advise programme sponsors and programme directors
• Define programme outcomes, scope, benefits and success measures aligned with client strategy
• Establish governance, decision rights, controls, tolerances and assurance processes
• Integrate programme plans, schedules, budgets, risks, dependencies and performance information
• Develop programme delivery approaches, resource plans and procurement strategies
• Build relationships with sponsors, governance groups, delivery partners and stakeholders
• Support organisational readiness, transition and benefits realisation
• Initiate, establish and deliver complex infrastructure programmes with clients, programme leaders and multidisciplinary teams
• Take increasing ownership of client relationships, coach emerging practitioners and contribute to programme management capability growth

Associate – Programme Management

• Process Individual Case Safety Reports (ICSRs) from all sources in compliance with applicable regulations, PrimeVigilance procedures, client-specific requirements, and timelines
• Perform ICSR follow-up, including SAE/SUSAR management, unblinding, clinical trial reconciliation, protocol review, and Safety Management Plan review
• Perform clinical and partner reconciliation
• Handle personal data protection activities
• Handle Product Quality Complaints and interact with Quality Assurance
• Interact with Medical Information
• Perform MedDRA and WHO coding
• Produce database outputs and reports, including data for monthly client reporting
• Manage workflow and resources
• Support pharmacovigilance processes within PrimeVigilance and for clients
• Perform tasks assigned to more junior positions as appropriate for a senior colleague
• Support the RA & PV Network Department as needed
• Act as LCPPV for the specified country as agreed with the line manager
• Take on the PRLS role for the designated language as agreed with the line manager

Senior Pharmacovigilance Associate

• Process Individual Case Safety Reports (ICSRs) from all sources in compliance with applicable regulations, PrimeVigilance procedures, client requirements, and timelines
• Perform ICSR follow-up activities
• Manage SAE/SUSAR activities, including unblinding, clinical trial reconciliation, protocol review, and Safety Management Plan review
• Perform clinical and partner reconciliation
• Handle personal data protection activities
• Handle Product Quality Complaints and interact with Quality Assurance
• Interact with Medical Information
• Perform MedDRA and WHO coding
• Produce database outputs and reports, including data for monthly client reporting
• Support workflow and resource management
• Support ICSR-related pharmacovigilance processes for PrimeVigilance and clients
• Perform tasks assigned to more junior positions as applicable for a senior colleague
• Support the RA & PV Network Department as needed
• Act as LCPPV for a specified country when assigned
• Act as PRLS for a designated language when assigned

• Process Individual Case Safety Reports (ICSRs) from all sources in compliance with applicable regulations, PrimeVigilance procedures, client-specific requirements and timelines
• Perform ICSR follow-up activities
• Manage SAE/SUSAR activities, including unblinding, clinical trial reconciliation, protocol review and Safety Management Plan review
• Perform clinical and partner reconciliation
• Handle personal data protection activities
• Handle Product Quality Complaints and interact with Quality Assurance
• Interact with Medical Information
• Perform MedDRA and WHO coding
• Produce database outputs and reports, including monthly client reporting data
• Manage workflow and resources
• Support pharmacovigilance processes for PrimeVigilance and clients
• Perform tasks assigned to more junior positions as appropriate for a senior colleague
• Support the RA & PV Network Department as needed
• Act as LCPPV for a specified country and PRLS for a designated language, as agreed with the line manager

• Process Individual Case Safety Reports (ICSRs) from all sources in compliance with applicable regulations, PrimeVigilance procedures, client requirements, and timelines
• Perform ICSR follow-up activities
• Manage SAEs/SUSARs, including unblinding, clinical trial reconciliation, protocol review, and Safety Management Plan review
• Perform clinical and partner reconciliation
• Handle personal data protection activities
• Handle Product Quality Complaints and interact with Quality Assurance
• Interact with Medical Information
• Perform MedDRA and WHO coding
• Produce database outputs and reports, including monthly client reporting data
• Manage workflow and resources
• Support pharmacovigilance processes related to ICSR management within PrimeVigilance and for clients
• Perform tasks assigned to more junior positions, where applicable for a more senior colleague
• Support the RA & PV Network Department as needed
• Act as LCPPV for the specified country and PRLS for the designated language, as agreed with the line manager