(Senior) Director of Project Office in Pharmacovigilance & Patient Safety (PVS)
PRA Health Sciences
EU
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We Are PRA.

We are 17,000+ employees strong, operating in more than 85 countries. We are committed to saving lives and we are constantly striving to be the best at what we do.

Our impact is real and we see it every single day. We are getting lifesaving drugs into the hands of those who need them most and continue to monitor products that are on the market for patient safety.

Who are you?

You are responsible for achieving business goals in accordance with the company mission and objectives. You are managing assigned initiatives in close cooperation with the Pharmacovigilance & Patient Safety Leadership.

As a true team player you know how to motivate teams to the best of their capabilities.

You want to learn from the best, grow your knowledge, your skill set, and you want to build your career here. You want to find a balance that still lets you be, well, you.

Most of all, you want to do it in a place where you’re more than an employee number. A place you love working.

Still here? Good. Because if this is you, we’d really like to meet you.

Responsibilities

What will you be doing?

As the ( Senior) Director PVS Project Office you will

  • Plan and lead implementation of the company / business unit (BU) strategy for build out or expansion of Pharmacovigilance & Patient Safety hubs in Europe, Asia and the Americas to provide pharmacovigilance services with high quality and in a cost-effective manner
  • Facilitate and lead change management initiatives, including integration of teams joining the organization from various backgrounds
  • Lead the implementation of the pharmacovigilance end to end service roadmap
  • Establish governance structure and report progress of all assigned projects to executive management and department management
  • Build and support strong teams within and across functional areas
  • Oversee the entire project life cycle from inception to close-out
  • Location : Preferably in one of our European or US Drug Safety Centers or optional Europe or North America remote.

    Qualifications

    What do you need to have?

    Skills :

  • Substantial experience in the pharmaceutical industry with broad experience in Pharmacovigilance
  • Track record in successful management of business improvement initiatives in the area of pharmacovigilance and patient safety
  • Substantial experience in leading and managing projects
  • Experience in working in a multicultural environment; experience in working with teams in Japan is a plus
  • Proven history of successful interaction with internal stakeholders
  • Effective written and oral communication including strong listening skills and excellent presentation skills
  • Ability to read, write and speak fluent English
  • Post-graduate degree or equivalent (Master’s Degree or PhD) from an accredited institution in medicine, pharmacy or other life-sciences
  • To qualify, applicants must be legally authorized to work in the European Union, the United Kingdom, the United States or in Canada and should not require, now or in the future, sponsorship for employment visa status.

    PRA is an EEO / AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.

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