Pharmacovigilance Officer

2 weeks ago

Johannesburg, Gauteng, South Africa Aspen Pharma Group Full time

Company Description:


We are a global speciality and branded pharmaceutical company, improving the health of patients across the world through our high-quality and affordable medicines.

Active at every stage of the value chain, we are uniquely diversi?ed by geography, product and manufacturing capability.

Aspen is a dynamic organisation built on entrepreneurial strength and forward-thinking minds. We attract high-performing individuals who are passionate about their career and have a desire to exceed expectations.

At Aspen, not only do we source for the best talent but we also provide a host of opportunities for continuous development.

The Group's key business segments are Manufacturing and Commercial Pharmaceuticals comprising Regional Brands and Sterile Focus Brands.

We have approximately 9 100 employees at 69 established offices in over 50 countries and we improve the health of patients in more than 150 countries through our high quality, affordable medicines.


MAIN DUTIES

PHARMACOVIGILANCE SUPPORT

  • ICSRs (Individual Case Safety Reports)
  • Performing assessment of adverse event case reports.
  • Act as case owner for assigned ICSRs to ensure accurate completion of data entry (DE), data review (DR) and regulatory reporting (RR), in line with current SOPs.
  • The PVO acts as a product owner for products under the remit of Pharmacare, supporting the PV Scientists with literature management and aggregate report preparation.
  • Maintain a high standard of case quality.
  • The PVO is responsible for providing a root cause analysis for any late reporting submissions.
  • Management and prioritisation of individual workload while maintaining good documentation practices (GDP).
  • Highlighting any safetyrelated issues to the attention of the management team.
  • Perform pharmacovigilance checks/evaluations of the Quality Assurance database (Trackwise Digital).
  • Reconciliation
  • Reconciliation
of all adverse event reports received by PV from internal stakeholders (QA/MIC and ACC).

  • Reconciliation
of all adverse event reports received from PV service providers, affiliates, distributors and license partners monthly, quarterly or bi-annually as described in the Safety Data Exchange Agreement (SDEA).

  • Quality Systems Management
  • Support preparation of SOPs, WIs, and product safety reviews
  • Raising of compliance cards for late cases reported to Pharmacare by service providers, affiliates, distributors and license partners.
  • Ensure all allocated CAPAs, Deviations and Actions are closed on time on Trackwise Digital.
  • Aggregate Reporting and Regulatory Intelligence
  • Keep abreast of changes to PV Legislation and ensure Regulatory Intel is monitored for ZA and SADC territories.
  • Basic PV training for all Aspen employees
  • Contribute to the development of PV training.
  • Pharmacovigilance training of all Aspen employees and distributors/service providers and documentation thereof.
  • Literature reviews
  • Regulatory review of key Medical Journals for any adverse drug reaction reports with Aspen Pharmacare products/medicines.
  • Understand SDEA obligations in order to ensure all aspects under agreements are duly executed.
  • Facilitate SDEA training (to employees as well as 3rd parties).
  • Signal management
  • Highlighting any safetyrelated issues to the attention of the management team
  • Coordinate Safety Review meetings (monthly)
  • Reviewing of Regulatory websites for any potential signals
  • All other ad hoc PV activity duties as required by the business needs
  • Adhere to agreed Key Performance Indicators (KPIs).
  • Support the continuous development and improvement of the PV function while upholding Aspen core values.
  • Receipt, evaluation and reporting of individual case safety reports in accordance with international (export territories) and local regulatory requirements and contractual partner obligations.
  • Provide support to Global PV.

CUSTOMER SERVICE

  • All queries are followed up and strictly within policy framework i.e. 48 Hours turnaround time.
  • A professional attitude is displayed when responding to a customer's needs.
  • Methods for improving customer services are proposed.
  • Internal and external customers are kept updated, under supervision, as to the progress of their queries
  • Liaise on a daily basis with RA customers, i.e. SAHPRA, Marketing, Manufacturing sites, Qualityrelated departments, Public Health, Exports, Outsource, and relevant licensors and distributors.

FINANCIAL

  • Identification of project challenges to departmental line management and the financial impact thereof

GENERAL

  • Ensure systems and procedures are in place in accordance with the RA QMS and that these are maintained according to the relevant SOPs
  • Adhere to agreed Key Performance Indicators (KPIs)
  • Support the continuous development and improvement of the PV function while upholding Aspen core values
  • Effective management and utilisation of resources to keep processes costeffective
  • Collating data for

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