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Job Details

Pharmacovigilance Manager – Take the lead for EU Safety and Medical Writing ** Global Projects **

Company: Advanced S&S (USA)
Location: Atlanta, Georgia
Reference: TMADV / 10386
Closing Date: 07 Jan 19
Type: Full Time
Salary (£): On Application
Benefits: On Application

Job Summary:

My client offers great career opportunities, flexible working hours, a strong salary and benefits package and a pipeline of over 30 indications in development. They are expanding in many areas including Pharmacovigilance and are now recruiting for a highly skilled and dynamic Pharmacovigilance Medical Writer based in Atlanta, US.

Requirements:

Location: Atlanta / Greater Atlanta, US

My client offers great career opportunities, flexible working hours, a strong salary and benefits package and a pipeline of over 30 indications in development. They are expanding in many areas including Pharmacovigilance and are now recruiting for a highly skilled and dynamic Pharmacovigilance Medical Writer who can work in regional and global project teams, with a strong voice, solid technical background and the ability to manage continuous improvement initiatives.

In return, you will have an elevated career path from an organisation  that is well known for providing a strong platform for career development and project leadership and sometimes team leadership. The benefits package is exceptional and  includes great flexibility around home working and a strong basic salary and bonus of up to 20%.  

The ideal profile will have strong experience in pharmacovigilance medical writing, extensive knowledge of formal requirements and guidelines; document, format, and content expertise; and writing, communication, and project management skills. You will play  a critical role in managing a high number of document files and versions, and ensuring that all contributions are provided and reviewed in a timely manner, as well as leading the document creation process and providing oversight and guidance to the multidisciplinary authoring team. Projects will be both regional and global and will cover all stages of development and lifecycle activities/initiatives  for an organisation that has a strong focus on career enhancement and unlocking innovation.

In essence, my client is looking for a highly specialised pharmacovigilance medical writer to ensure clear data presentation, effective medical communication, and content - and stylewise consistency across modules.
If you are looking for a role where you will be  part of driven and patient-focused cross-functional teams, participating in mentoring and developing effective working relationship with vendors, and project managing continuous improvement initiatives, for a successful and expansive Biotechnology company, then this could be the role for you!  Please call or email today in confidence, to discuss this role in more detail.

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If you wish to apply for this role, please send your CV with a covering note to cv@advregulatory.com or alternatively, to have a confidential discussion about this or other potential roles or career options, call Theo Moore in the London office on +44 (0)20 7801 3384 or dial Toll Free from the US on 855 505 1382..
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About Advanced

Advanced Regulatory is a division of Advanced Search and Selection Ltd and has been operating since 2004. We are registered and licensed to recruit through the United Kingdom, mainland Europe and the Americas - we have offices both in the UK and in Switzerland. We are a recruitment business dedicated to the pharmaceutical industry, specialising in Regulatory Affairs.

We match professional candidates to the best permanent, contract and interim roles in the market.

We provide a high level of service because we believe this matters. Regulatory professionals will find we know our recruitment subject matter.

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To Apply : Please send a full CV in confidence to cv@advregulatory.com.

Contact Information:

Address:  Head Office
Suite 8 Penhurst House 352-356 Battersea Park Road London
SW11 3BY
England
Tel:  +44 (0)207 801 3380
Website:  Visit Our Web Site

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