Pharmacovigilance Medical Writer – Regional and Global Projects ** North Carolina

Reference: TMADV10386

Expiry Date: 05-11-2019

Category Regulatory Affairs

Salary: Competitive

Job Type: Full Time

Location:
Durham County
United States

Apply for position

Job Description

 

Location: North Carolina, 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 style-wise 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.

 

To Apply!

To apply for this role, please register on this web site. My team and I would welcome a phone call in private if you would like to explore this role and opportunity, then please contact either myself, Theo Moore, or my colleague Matt Greig, in the London office on +44 (0)20 7801 3384, or at any time during evenings on +44 (0)7918679405.

GDPR & Data Protection: Your information is safeguarded for GDPR, and you will have the right to edit, amend or delete and ’’be forgotten’’ at any time after your initial registration.

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.

Keywords / Key words: UK PV Jobs, Vacancies Medical Writer, Pharmacovigilance Jobs, PhV Jobs, Regulatory, Regulatory Affairs, Reg Affairs, RA, Regulatory jobs, RA jobs, Regulatory Affairs Jobs, Drug Safety, PhV Jobs, PV vacancies, Medical Writer, US Jobs, Medical Writer US Jobs.