Site Name: UK – London – New Oxford Street, Belgium-Wavre
Posted Date: Nov 15 2024
Are you energized by the opportunity to work with global stakeholders to design, deliver and embed critical highly visible safety programs that have a global impact? If so, this Safety Pharmacovigilance Director role could be an ideal opportunity to explore.
As a Safety Pharmacovigilance Director, you will play a key role in supporting the Central Safety Leadership Team, and the broader business at both a strategic and operational level.
This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following…
* Deliver strategic solutions and lead the implementation for key organizational/process changes ensuring that GSK can comply with pharmacovigilance regulations worldwide.
* Develop strategy and lead the implementation of core business activities (e.g. Communications, Information Management, Training), seeking endorsement from the Central Safety Leadership team; provide ongoing, thoughtful program management and change management support to ensure delivery against a strategic agenda.
* Lead the review and re-design of critical business processes; deliver solutions that align across business units; develop and lead training/change management activities.
* Provide specific subject matter expertise on relevant business processes to ensure regulatory compliance and appropriate management of risk across GSK (to include authoring process documents, adhering with evolving regulatory requirements, delivery of training and the proactive identification of potential compliance risks).
* Secretariat to Central Safety governance boards/leadership teams as appropriate; ensure appropriate/timely agendas/minutes (to include action tracking) based on input from stakeholders; provision of appropriate project management leadership.
* Project management support for the business change initiatives/process updates to include driving the development and tracking of business plans (including objective setting, Key Performance Indicators, benefits tracking).
* Line manage scientific/technical associate staff who support specific business activities including provision of metrics, information management, communication and website related deliverables (as needed).
Why you?
Basic Qualifications:
We are looking for professionals with these required skills to achieve our goals:
* Bachelor’s degree.
* Prior experience managing multiple strategy formulation and change projects.
* Experience with Pharmacovigilance processes and global Pharmacovigilance regulations.
Preferred Qualifications:
If you have the following characteristics, it would be a plus:
* Advanced Degree Life Sciences or Pharmacovigilance.
* Professional certification in Project management.
* Ability to effectively influence key stakeholders at all levels of the organization.
Why GSK?
Our values and expectations are at the heart of everything we do and form an important part of our culture.
These include Patient focus, Transparency, Respect, Integrity along with Courage, Accountability, Development, and Teamwork.
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK.
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