This site uses cookies. By continuing to browse the site you are agreeing to our use of cookies. Find out more here.

Close Message
NextPharmaJob.com for pharmaceutical industry jobs
NonStop Recruitment
NextPharmaJob.com is dedicated to putting job seekers looking for pharmaceutical industry jobs in touch with recruiters and employers.

Similar jobs you may be interested in:

Clinical Project Manager - Poland
Poland
Principal Scientific Assistant – Hazard classification (Strasbourg - France)
France
Clinical Trial Scientist - Oncology
Switzerland
Chief Development Officer - Biotech
Denmark
Digital Product Owner
Germany
More...

To receive a FREE weekly email alert of all the latest pharmaceutical industry jobs added to our database enter your email address below.

Submit | Tell me more...

Sister sites:
Our sister site Our sister site
Partner sites:

At Burntsky Limited we work with a number of third parties in order to maximise the reach of the jobs posted with us including but not limited to:

JooblePartner Jooble
UK Jobs
Science Jobs

Job Details
This job has expired. Click here to view similar jobs.

Regulatory Writer - A chance to spend 9 months in Switzerland



Business Type: Drug Development Company
Job Type: Clinical Development
Job Level: Experienced (non manager)
Position: Contract
Location: United Kingdom
Reference: KA291066_2
Closing Date: 11/06/21
Job Details:

Our client is a high-potential biopharmaceutical company, specialized in the discovery, development and commercialization of innovative small molecules, with the aim of transforming the horizon of therapeutic options.

You have an opportunity to experience living in one of the best places in Europe - Switzerland. This is an exciting chance to gain irreplaceable experience, both professionally and personally.

The company is now looking for a Regulatory Medical Writer on a 9-month fixed term contract basis for maternity cover, you can start as soon as 1st of July.

This position is responsible for the development of high-quality clinical documents for submissions to regulatory authorities globally and works directly with multidisciplinary project teams.

Job Responsibilities include :
* Write and/or review clinical regulatory documents such as clinical study reports and NDA/MAA submission documents
* Act as a lead medical writer for submission documents and contribute scientifically and strategically at the project and/or study team level to facilitate efficient development of high-quality clinical documents for regulatory filing
* Act as subject matter expert for regulatory requirements within clinical study and submission teams to ensure compliance of documentation to internal company standards and external regulatory guidelines
* Effectively collaborate with cross-functional stakeholders, including Therapeutic Area, Clinical Pharmacology, Biostatistics, Drug Safety, Clinical Operations, Preclinical Research, and Drug Regulatory Affairs
* Work together with the in-house Editorial Group to produce high-quality final documents and ensure timely delivery


Candidate''s Requirements
* University degree in life sciences or other relevant scientific discipline required. An advanced degree is desirable
* English mother tongue, or excellent spoken and written English
* 5+ years as a medical writer in the pharmaceutical industry across several therapeutic areas

To be eligible to be successful Swiss work permit or EU passport is required.

If you are interested, I will be more than happy to arrange a call and tell you all the details about this position and more.

You can reach me by phone or by email: +44 207 940 2100 (ext.3508) or k.aleksandraviciute@nonstop-recruitment.com



Posted: 04/06/2021 | NPJ Ref: 272110
line graphic

Compatible with:

JobMate   Broadbean   Idibu

Site optimised for Internet Explorer 8+ / Firefox 3+
View a complete Jobs Listing




Credit cards image