The role of the Global Pharmacovigilance (GPV) Training Program Coordinator is to establish, maintain and execute comprehensive training programs across business units (Global Pharmacovigilance, R&D, Quality/Manufacturing, and Commercial), assure global training compliance to internal/external requirements, collaborate with Corporate Communications for rollout of Annual Pharmacovigilance Awareness Training and act as a subject matter training expert for the global Pharmacovigilance community. In this role, the Pharmacovigilance Training Coordinator may also work on special projects as necessary.
Primary Responsibilities include (but not limited to) the following:
Act as the Subject Matter Training Expert for Global PV
Development, oversight and monitoring of compliance for the Pharmacovigilance training curricula.
Development, roll out and, as necessary, delivery of specific pharmacovigilance related trainings
Accountable for the objectives related to the GPV Training program
Ensure adequate documentation and training is provided to all staff involved in PV related activities
Establish and maintain GPV SOPs, Work Instructions and Training Guides
Support Agency related topics such as PSMF and Agency Inspections in relation to the Pharmacovigilance Training programs and compliance
Experience and background:
Bachelor's degree in science or related field.
Demonstrated relevant experience gained in Global Pharmacovigilance or another regulated environment.
Experience with Pharmacovigilance databases preferred.
Experience with developing and delivering training programs preferred
Technical Skills Requirements:
At a minimum:
Possess detailed understanding of what it takes to be an effective support to colleagues / teams in a multicultural, dynamic, and constantly changing environment.
Demonstrate a high level of competency using Microsoft Office suite - especially in Microsoft Word and Excel.
Exhibit effective communication skills in English (both written and oral) with colleagues at all levels of the organization and external regulatory agencies.
Consistently model behaviors of accountability and ownership through approachability, excellent interpersonal, communication, negotiation, and problem-solving skills.
Ability to work independently, while fostering good working relationships across physical distance and have flexibility and the capacity to handle multiple tasks at once.
Highly effective team player and creative problem solver
Desirable
Experience of Pharmacovigilance practices
Experience with Zoetis' Global Pharmacovigilance Database
Familiarity and experience with building training programs and executing training of others
Experience of dealing with Zoetis Regulatory Managers across all geographies
Experience with conducting Business Objects reports
Full time
Regular
Colleague
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