Jobs

JUNIOR MEDICAL WRITER

Job Description

The Junior Medical Writer will be involved in the writing of clinical regulatory documents and assist the senior medical writers when needed. 

If you would like to be part of an enthusiastic team and you meet the specifications below, don't hesitate to contact us.

Duties and Responsibilities

• In-time generation of clinical documents
• Compilation of clinical documents in accordance with SOPs and GCP
• Gain and maintain knowledge through attendance of workshops and conferences

Qualifications

University degree (MSc or PhD from a reputable university) in a biomedical or related discipline with a passion for writing scientific documents.

Job Requirements

• Strong desire to gain experience in medical writing
• Fluent English (oral and written) and familiar with medical and scientific terminology
• A scientific background linked to medical science
• Eye for detail
• Good computer skills especially Microsoft Office
• Good communication and organizational skills, and stress resistant
• Teamplayer
• Own car and legal drivers license

In return...

... EMTEX offers the opportunity to develop your medical writing skills in a supportive and rewarding environment.

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Contact Information

Interested? Please send your application letter with an indication of your motivation and experience together with your CV to mario.de.witte@emtex.be or by mail to EMTEX BVBA - Mario De Witte - Heistraat 99 - 9190 Stekene.

SENIOR MEDICAL WRITER

Job Description

A Senior Medical Writer prepares and reviews clinical regulatory documents. Further responsibilities include: communication with clients for medical writing projects, meet timelines, leadership, and training and support of junior medical writers.

Duties and Responsibilities 

• Writing clinical documents for submission
• Reviewing of draft and final documents prepared by other writers before distribution
• Ensure that content and style of documents adheres to regulatory guidelines and complies with client SOPs and guidelines
• Attend client team meetings and internal meetings related to the medical writing project
• Provide training and guidance to junior medical writers
• Keep ahead of information and technology through workshops and conferences and transfer the information to other team members

Qualifications

University degree (MSc or PhD from a reputable university) in a biomedical or related discipline and at least 5 years experience as a Clinical Medical Writer at a pharmaceutical company or international contract research organization. 

Job Requirements

• Fluent English (oral and written) and familiar with medical and scientific terminology
• Excellent in scientific interpretation/presentation of data and understanding of biostatistics
• Broad knowledge of FDA en EMA guidelines
• Eye for details
• Good computer skills, especially Microsoft Office
• Good communication and organizational skills, and stress resistant
• Ability to work independently and in the study team, be able to manage multiple tasks
• Client focused approach, professional attitude
• Teamleadership & positive team-oriented attitude
• Own car and legal drivers license

In return...

 ...EMTEX offers a competitive compensation, with a comprehensive benefits plan in a supportive and rewarding environment.

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Contact Information

Interested? Please send your application letter with an indication of your motivation and experience together with your CV to mario.de.witte@emtex.be or by mail to EMTEX BVBA - Mario De Witte - Heistraat 99 - 9190 Stekene.