Please find it here https://onlinemedicalwriting.com/blog/2020/03/17/how-to-become-a-succesful-medical-writer/

Dutch Speaking Medical Writer freelance job vacancy medical writing for new business healthcare advertising pitch. Start work ASAP. West London healthcare advertising agency.
To apply click here : http://bit.ly/dutch_medical_writer #DutchJob #DutchSpeaker #MedicalWriter #FreelanceJob

The Principal Medical Writer researches, writes and edits clinical reports, summarizing statistical data from clinical studies, writes clinical study protocols, clinical plan outlines and sections of regulatory submission documents by applying therapeutic expertise and clinical drug development knowledge and relevant experience to the development of drugs, biologics, devices and or other products for human use.

Responsibilities:
Acts as a Lead medical writer on a program, numerous individual studies, or other projects at a simple to complex level.
Acts as Lead medical writer on simple to complex submissions projects.
Provides leads for Business Development opportunities.

Minimum Qualifications
Substantial experience in pharmaceutical or CRO industry developing pharmaceutical drugs for human use required e.g. non-clinical science, medical related writing, protocol writing, writing for regulatory submissions, clinical trials management, monitoring, or as an investigator or sub-investigator for clinical trials

Substantial experience writing clinical study reports, other regulatory submission documents, poster presentations, and manuscripts for publication in a scientific journal required

Experience using computerized systems (PC-Windows, and MS Office) required

Knowledge of regulatory agency requirements for protocols and regulatory submissions in the host country required

Direct or indirect experience interacting with FDA or host country regulatory agency required

Demonstrated project leadership skills required

Read, write and speak English; fluent in host country language required
In addition to the above must have experience complex science or medical related writing experience required
An advanced degree (M.S., PharmD, Ph.D.) from an accredited institution in science or a health-related field, or equivalent international education preferred. Bachelor’s degree in scientific, health-related or journalism/ communications required

To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status

PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.

CLICK TO APPLY TODAY!

Principal Medical Writer

For anyone interested in consumer health writing, I've put together a few free guides and resources to help you get started - you can read them online or download to your desktop to read later! I hope you find them useful - https://www.healthwriterhub.com/health-writing-guides/ 

Enroll in Talent Hunt – 2019 and win a chance to be a professional Medical writer!

Everyone who understands science and are avid writers are invited to Participate, Write and Win I-CME – Medical Writing and Healthcare Communications User Licence.

Registrations open till 25th August 2019

Enroll today - https://www.onlinemedicalwriting.com/icme-talent-hunt

Talent Hunt 2019 – A Scientific Writing Contest invites Pharma, Medical and Healthcare enthusiasts to be a Part, Write and Win I-CME – Medical Writing and Healthcare Communications User Licence.

Registrations open till Aug 25th 2019

To register - https://www.onlinemedicalwriting.com/icme-talent-hunt

UC San Diego Extension is hosting  a workshop titled Expert Strategies and Skills for Medical and Scientific Communication on the UC San Diego campus June 21, 2019. This one day workshop is bringing together expert faculty and life science leaders who represent a variety of writing, research, and medical educational backgrounds.  For more information and to register:   https://extension.ucsd.edu/MedSciComms

Vado Med Tech are retained as the exclusive partner for a multi-award-winning Consultancy that employs over 900 staff worldwide with a culture focused on excellence, continuous improvement and collaboration. They have a unique position in the Consulting space with physical laboratory services, clinical research teams in addition to Consulting services bringing devices to market across the world.

They have an unrivaled presence in the medical device, human tissue and IVD space and have already made substantial investments in the European and US infrastructure to support and facilitate this growth.

Due to continued expansion and customer demand they are appointing additional Medical Writers to their existing team of around 20 who work remotely across Europe in either the UK, France, Belgium, Finland, Netherlands or Germany. They have an unrivalled presence in the medical device, human tissue and IVD space and have already made substantial investments in the European infrastructure to support and facilitate this growth.

You can expect a huge variety of work in an array of therapeutic areas that will broaden your skills and knowledge. Our client likes to employ staff who have a desire to develop and challenge their abilities. Actively encouraging personal development giving exposure to projects that will require substantial research and collaboration.


Responsibilities:

As Medical Writer you will:

- Write, edit and review PMA's, 510ks, CER's (Clinical Evaluation Reports), Technical Files, Design Dossiers, Instructions for Use, labeling and internal documents for medical devices and human tissue products.
- Coordinate with internal stakeholders in Consulting, Project Management and externally with the client.
- Provide medical writing, editorial and peer review support for publications, posters, white papers and promotional material.
- Document QC
- Liaise with other medical writers on developing best practice in writing style, harmonisation of terminology and team initiatives.

Your profile:

You will have experience writing technical regulatory documentation for medical devices including CER's. Practical exposure to the requirements of Rev4 would be beneficial. A higher level education is expected in a relevant subject. Any language capabilities in addition to English could be beneficial.

Interviews will be conducted over the coming weeks via WEBEX. You can expect a Consultant from Vado Med Tech to contact you within 48 hours of application.

This role is 100% remote, using online WEBEX and other web tools to interact both internally and externally. You are able to work anywhere within the UK, France, Germany, Netherlands, Finland or Belgium. Fluency in English is essential. It will suit a self starter who is happy to work as a subject matter expert and have virtual interaction with key team members and customers.

Direct link to apply: https://jobs.vadomedtech.com/Medical-Writer---Remote-based-United-Kingdom-15

Good Afternoon Krish,

I am working on a number of Medical Writing opoortunities all across Europe. With global expansion, my client is looking for candidates who have key regulatory writing experience. Once you have received this message, please do send me an email and we can talk further: bthompsett@barringtonjames.com

Regards,

Ben

Hi All,I do have below requirement which is for our Direct client. Please let me know your are interested.Role: Medical Writer

Location: Woodcliff
Lake, NJ

Duration: Contract

 

Job Description:

Work
directly with clinical study teams, the Oncology medical writing
teams, regulatory affairs personnel, and the publishing group in the
preparation of scientifically valid regulatory documents. Responsibilities include
preparation of regulatory documents on behalf of Eisai in accordance with the
ICH guidelines, international regulations, Eisai standards and processes, and
the Eisai Writing Style Guide as applicable. Documents include but are not
limited to: Protocols and protocol amendments, clinical study reports,
Investigator brochures, and submission documents. Participate in project team
meetings to provide input regarding deliverables, timelines, and processes.
Responsible for managing the document review process. Route documents for
approval. The medical writer should be familiar with ICH
guidelines and the current AMA Style Manual. The writer will be
expected to format and manage long documents with multiple review cycles and
tight deadlines.

Qualifications:

·        
Bachelor's
degree in life sciences, RN, Master's degree in life sciences, PharmD or PhD
preferred.

·        
Excellent
regulatory writing skills, meticulous attention to detail, proficiency using an
electronic document management system and standard style guide, and strong
analytical ability to interpret clinical data.

Experience: 5+ years’ writing experience in the
pharmaceutical industry.

We
are looking for someone with experience working as a MW for a major Pharma.
Prior experience in oncology is a plus. The most important requirement is the
ability to independently write regulatory documents in collaboration with the
various members of study team.

Hello All,

I have super instructions to recruit Medical Writers for jobs in London and Amsterdam.

Positions range from Associate to Senior.

Material ranges from Manuscripts to eLearning. 

To view the jobs click here : 

Medical Writer : Amsterdam : eLearning and Events : https://www.pharmemed.com/jobs/medical-writer/766 

Publications Manager : London : manuscripts, posters, book reviews : https://www.pharmemed.com/jobs/publications-manger/765 

Associate Medical Writer : Amsterdam : https://www.pharmemed.com/jobs/associate-medical-writer/768 

Associate Publications Manager : London : https://www.pharmemed.com/jobs/associate-medical-publications-manager/769

Connect with me here : george@georgebuckland.com 

Hi, I’m the managing editor at Sharecare.com, a consumer health and wellness site created by Jeff Arnold (founder WebMD) and Dr. Oz.

We’re hiring for two positions: social media manager (SMM) and senior medical editor. Office location: Jersey City (soon to be NYC).

For the SMM job, consumer health experience is required. See listing for more details.

For the senior medical editor, medical writing/editing experience is a must! This person should be comfortable translating medical studies, jargon or concepts into digestible, consumer-friendly content.

Interested and qualified? Email me your resumes: Nancie.George@sharecare.com

Thanks!
Nancie

https://workforcenow.adp.com/jobs/apply/posting.html?client=sharecare&ccId=19000101_000001&type=MP&lang=en_US

Hi!

I am currently working at a CRO in India. However, I am actively seeking out new opportunities. Please send me a message incase you are interested, thanks!

I'm training at the Graham School of Liberal Studies and Professional Development, which is associated with the University of Chicago. I have one course (of four required) to go for a certificate. So far, no bites from employers to whom I have applied. 

Where are you looking?

Hi

any medical Writers? Can we talk training and opportunities?

Dear all, I am a media practitioner with experience in publishing, online profiling, writing, PR/Advertising. I currently develop content for www.cityscope.ng and other copy-writing/advertising agencies. A working professional with many years of expertise in educational entertainment, content development, project and events management, marketing, product review and branding. I have acquired desired knowledge set in international standards. Having the ability to manage and develop staff, whilst at the same time balancing any changing and potentially conflicting demands on resources. Area of expertise is content writing, PR/Advertising, Events reporting         Corporate Brand Identity Development ·         Social Media Marketing ·         Executive Profile Optimization       Here is the link to my linkedin profile https://www.linkedin.com/in/johnolubukunmifatanmi/      I am open to collaborations and job opportunities with an organization that provides me the opportunity to show my full potentials. I can be reached via fatanmijohn@gmail.com  ·         

Hello everyone, I am looking for medical writing/editing jobs in San Francisco city or the bay area in California, US. After
having worked for two years as a Senior Cell Process Engineer in a cord blood
bank, I entered the field of medical/scientific editing and medical
communications three years ago because I strongly believe that the lack of
ability to communicate well should not hamper the growth of science. As an
Associate Editor at a scientific communications company, I worked with several
clients who had great scientific expertise but could not disseminate their
knowledge to the international scientific community due to several reasons.
This experience further increased my interest in the field of medical/scientific
editing, as I learned that my knowledge of editorial and publication practices
and my educational background could be put to good use to contribute to the growth
of the international scientific community.

During my tenure at my
previous company, I have edited and helped in the publication of over a
thousand research manuscripts from different fields of biology such as Cell
Biology, Developmental Biology, Genetics, Molecular Biology, and Molecular
Oncology. I am also well versed with the ethical guidelines related to
scientific and academic publications and have complete knowledge of the peer
review process. My role as an editor also
involved constant communications with clients that were aimed at catering the
edits to their requirements, which greatly helped me polish my communication
skills. Please let me know if any one here knows of any opportunities for me.Thanks!