Associate Director of PV Operations - Switzerland

Location
Zürich
Salary
Negotiable
Posted
Apr 16, 2018
Closes
May 16, 2018
Ref
RP.185662.2
Contact
Reka Peterfi
Organization Type
Corporate
Contract Type
Employee
Hours
Full Time

Associate Director of PV Operations - Switzerland


I am searching for an Associate Director of Pharmacovigilance (PV) Operations that is a creative, resourceful and an integrative problem solver. If you have been accused of being an "Outside of the Box" thinker, do not hesitate to read below!

I am looking to speak to you if you are not afraid to overcome challenges and to get your hands dirty, because I believe this role is for you.

This position is responsible for creating, directing and managing the company's infrastructure to support the operational aspects of the pharmacovigilance system and to make sure that all processes and personnel adhere to global regulatory requirements and internal processes and procedures.

If you have good stakeholder management skills and you are passionate about maintaining excellent relationships with key strategic internal and external stakeholders (including the hiring and training of Drug Safety and Pharmacovigilance personnel) email me and I will be happy to give you more details.

You will be the Go To Guy for:

* Expert guidance and leadership both internally and externally for the development and post-marketing safety requirements, per ICH; US and international regulations and guidelines; and Good Pharmacovigilance Practice (GPvP).
* Support for Building and implementing pharmacovigilance systems fully compliant with the applicable worldwide Health Authority PV regulations.
* Advice for the Developing and implementing an inspection readiness program
* Management Plans and set up of safety systems and database configurations in the PV database to accommodate these trials and products.
* Optimising, implementing change and Improving

Nice to have:

* Around 8-10 years of experience in Drug Safety / Pharmacovigilance Operations
* Demonstrated ability to create, evaluate, and maintain effective business processes and implement procedures, systems, and tools to maximize resources within a Drug Safety department
* Knowledge of clinical and post marketing processes
* Exposure to different Regulatory requirements and several global and regional Authorities
* Operational expertise with PV Databases
* "Je ne sais quoi" for building and creating new worlds

What's in it for You:

* The professional satisfaction of optimising/changing the PV Department of a global player
* Amazing and welcoming company culture
* Excellent Benefit Package
* Unique boost for your resume

For a confidential discussion about this role and to take a positive step to your next role call me and I will be happy to discuss further details with you or anyone from your network, whom you recommend.

You can contact me at Reka Peterfi: +41 435 080 817, extension: 3344 or email me your CV in Word format: R.Peterfi@nonstop-pharma.com.

Nonstop is one of the largest and fastest growing specialized life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland and the Czech Republic and we hold labour leasing licenses across Europe. Please visit our website for a full list of the niche markets we cover.

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