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:
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
Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume.
Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search.
Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at zoetiscolleagueservices@zoetis.com to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at www.Zoetis.com/careers site, or (2) via email to/from addresses using only the Zoetis domain of "@zoetis.com". In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.