Medical Writing vacatures
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- EmtexSint-Gillis-Waas
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- CognizantBrussel-Hoofdstad
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Senior Medical Writer (Europe)
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- Experience with writing of protocols, CSRs and CTDs.
- To write and edit complex medical writing deliverables (…
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Job Post Details
Junior Medical Writer - job post
Sint-Gillis-Waas•Thuiswerk
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Vacaturegegevens
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EMTEX is an independent and compact company that offers professional medical writing and related services all around the world to the pharmaceutical (human & veterinary), biotech, medical device and other industries, CROs and academic institutions. We have a long track record in supporting our customers with dedicated services. As we would like to expand our international services, grow and strengthen our team, we have a job opening for a Junior Medical Writer.
JOB DESCRIPTION
Successful candidates will assist in the preparation of a wide range of clinical and regulatory documents, including Investigator Brochures, Clinical Study Reports, Clinical Trial Protocols, Clinical Summaries of Efficacy and Safety and Clinical Overviews. The documents must be of high quality in terms of scientific content, organization, clarity, accuracy, format and consistency, and must adhere to regulatory guidelines and company styles and processes.
JOB TYPE
Full-time (40 hours per week); in office/home office.
PRIMARY LOCATION
Belgium (Sint-Gillis-Waas) or The Netherlands
ROLES & RESPONSIBILITIES
Assist more experienced Medical Writers in the preparation of simple documents.
Supported by a Senior or Specialist Medical Writer, write clear, concise, and consistent simple documents compliant with the needs of the regulations or questions of the authorities, as appropriate.
Perform literature searches/reviews as necessary to obtain background information and training for development of documents
Model a rigorous and disciplined approach to medical writing
Ensure that all work is complete and of high quality (and adhere to the instructions from the more experienced Medical Writer)
Ensure document content and style adhere to FDA/EMA or other appropriate regulatory guidelines, and comply with internal and client SOPs/WIs and style guidelines
Attend (or lead) internal and client team meetings as required
Orchestrate an effective and efficient document review process
Perform Quality Control checks of documents.
EDUCATION
A minimum of a Master’s degree in a scientific discipline (a degree in biological, veterinary, pharmaceutical or medical sciences) is highly preferred.
EXPERIENCE
Relevant experience will be considered an advantage. A pronounced passion for writing is key!
SKILLS & COMPETENCES
Have/develop an eye for detail
Further improve spoken and written English
Demonstrate excellent computer skills
Be a good communicator
Have a team-oriented attitude
Act/behave professionally with a client focus
Be pro-active
Always be eager to learn
Further improve your writing skills
Take ownership/responsibility of your document
Be well organized
LANGUAGE
Excellent written and verbal language skills in English and Dutch (C1 or better).
OUR OFFER
We offer a competitive salary package.
CONTACT INFORMATION
Interested? Send your motivation letter and CV (attn. of Mrs. Griet Van Acker).
Emtex BV
Hoogeindeken 8L
9170 Sint-Gillis-Waas
JOB DESCRIPTION
Successful candidates will assist in the preparation of a wide range of clinical and regulatory documents, including Investigator Brochures, Clinical Study Reports, Clinical Trial Protocols, Clinical Summaries of Efficacy and Safety and Clinical Overviews. The documents must be of high quality in terms of scientific content, organization, clarity, accuracy, format and consistency, and must adhere to regulatory guidelines and company styles and processes.
JOB TYPE
Full-time (40 hours per week); in office/home office.
PRIMARY LOCATION
Belgium (Sint-Gillis-Waas) or The Netherlands
ROLES & RESPONSIBILITIES
Assist more experienced Medical Writers in the preparation of simple documents.
Supported by a Senior or Specialist Medical Writer, write clear, concise, and consistent simple documents compliant with the needs of the regulations or questions of the authorities, as appropriate.
Perform literature searches/reviews as necessary to obtain background information and training for development of documents
Model a rigorous and disciplined approach to medical writing
Ensure that all work is complete and of high quality (and adhere to the instructions from the more experienced Medical Writer)
Ensure document content and style adhere to FDA/EMA or other appropriate regulatory guidelines, and comply with internal and client SOPs/WIs and style guidelines
Attend (or lead) internal and client team meetings as required
Orchestrate an effective and efficient document review process
Perform Quality Control checks of documents.
EDUCATION
A minimum of a Master’s degree in a scientific discipline (a degree in biological, veterinary, pharmaceutical or medical sciences) is highly preferred.
EXPERIENCE
Relevant experience will be considered an advantage. A pronounced passion for writing is key!
SKILLS & COMPETENCES
Have/develop an eye for detail
Further improve spoken and written English
Demonstrate excellent computer skills
Be a good communicator
Have a team-oriented attitude
Act/behave professionally with a client focus
Be pro-active
Always be eager to learn
Further improve your writing skills
Take ownership/responsibility of your document
Be well organized
LANGUAGE
Excellent written and verbal language skills in English and Dutch (C1 or better).
OUR OFFER
We offer a competitive salary package.
CONTACT INFORMATION
Interested? Send your motivation letter and CV (attn. of Mrs. Griet Van Acker).
Emtex BV
Hoogeindeken 8L
9170 Sint-Gillis-Waas
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