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Job Details
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Senior Medical Writer (Europe) - Highest Standards!

Business Type: Clinical Research Organisation
Job Type: Medical Writing and Editorial
Job Level: Experienced (non manager)
Position: Full Time
Salary: EUR60000 - EUR70000 per annum
Location: Poland
Reference: TB299687-12
Closing Date: 23/09/21
Job Details:

A fast growing family owned company is having couple of new roles open up around Europe (Italy, Spain, Poland, France, UK, Germany, Belgium, Netherlands, Sweden, Switzerland (Ticino)). For Senior Medical Writers for permanent positions.

The company works with some of the biggest pharmaceutical companies in the world, with a very high standards work environment and continues growth. Which provides the best environment to learn, improve your skills, and grow exponentially.
They also offer a supportive working environment, great personal career development and challenging projects. Not to mention that the vast majority of the promotions happen internally.

What makes the role/company interesting?
* The company is family owned, not solely focused on profit.
* There is future scope for growth within the business.
* They don''t just do Oncology and oncohematology but also CNS, Orphan and smaller studies in other areas. Which gives an exceptional variety of projects to work on.
* This role can offer a lot of new experience to further develop your career.

Duties & Specific Tasks:
- Draw up, edit and review preclinical/clinical documents such as clinical study reports, study protocols, patient information and informed consent forms and other medical and regulatory documents;
- Develop scientific manuscripts and abstracts reporting clinical study results, as well as slide and poster presentations;
- Prepare regulatory and preclinical/clinical documents for drug development and registration activities;
- Liaise with Biometrics staff, Pharmacovigilance and Clinical Operations Units for information or guidance, as necessary;
- Coordinate and manage documents to be sent to customers;
- Perform literature searches and reviews necessary to obtain information for the development of documents;
- Work in accordance with Regulations, Good Clinical Practices and ICH guidelines and Company Standard operating Procedures;
- Create and maintain audit trail of all the document changes;
- Review the quality and accuracy of the documents in English.

Skills and experience
* Required communication languages: English
* 3-5 years'' experience, or more.

What NonStop offers:
* Your own designated consultant and one point of contact
* CV review service
* Wide range of Pharma Work Roles throughout Europe
* Interview advice and preparation
* Consultants with experience
* A supportive team who can always deal with your queries
* Advice

If you''re interested in this or any other vacancy, then send over your CV, preferably in a Word format.
If you''re not interested at the moment perhaps you know someone who is? We offer a referral fee, you could make a friend very happy and have some extra cash for yourself.

For a confidential discussion about this, or many other opportunities throughout Europe, please get in touch with Taqi Ben at NonStop Pharma, or on Linkedin.

NonStop is one of the largest and fastest-growing specialized life-sciences & Med-tech 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, Romania, Luxembourg, the US, and the Czech Republic and we hold labor leasing licenses for all EU8 countries. Please visit our website for a full list of the niche markets we cover.

Posted: 16/09/2021 | NPJ Ref: 282762
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