This role will work alongside designers and project managers to ensure complex concepts are translated into engaging and educational content within the given……
The Medical Writer will create, research, edit and coordinate the production of clinical documents related to independent review, including independent review……
Play an active role in client calls. Contributes to internal status calls to keep the team updated on actions. Maintains an average billability of 85–90%.…
We offer unique opportunities to collaborate on client projects that are highly visible and are engaged in inspiring pharmaceutical products and technologies……
In this role, you will author clinical study reports, protocols, consent forms, narratives, and investigator brochures while collaborating with clinical teams……
Establish standardized processes for study design, data requests, analysis, and publication timelines. We may use artificial intelligence (AI) tools to support……
*Advanced Scientific Training: *Ph.D., M.D., Master’s degree, or equivalent advanced training in biology, medicine, health sciences, public health, or a related……
Master’s or PhD degree in Science or related field. Utilizes scientific and clinical expertise, along with advanced writing and analytical skills, to research,……
Bachelor's degree in Life Sciences, Pharmacy, Medicine, or related field, with a keen interest in medical writing, clinical research, and drug development……
Provides strategic direction to cross-functional project teams with minimal oversight to ensure that clinical documents (eg, Investigators' Brochures [IBs],……
Supporting all phases of drug development, we provide end-to-end technical solutions to our clients including *1)* *Clinical Pharmacology 2) Pharmacometrics and……
An innovative clinical-stage biotechnology company is seeking a Senior Director, Medical Writing to provide strategic and operational leadership for clinical……
This Technical Writer will author and revise Instructions for Use and electronic IFU content for regulated medical devices using structured XML-based authoring……
Independently review personal injury case files and determine whether they are ready for demand preparation. Assist with additional pre-litigation writing, file……
Bachelor’s Degree in a business, science, or related field. The Senior Business Development Director - Regulatory & Medical Writing is responsible for driving……
We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic……
The ability to keep calm under pressure, work on multiple projects in parallel and meet agreed deadlines. Reviewing and providing constructive feedback on the……
In addition to consistently evolving and expanding your own understanding of your markets, you will effectively communicate relevant information to internal……
Our team works with experienced healthcare professionals and medical experts to research and review educational content covering a wide range of health topics,……
Experience supporting message-driving narratives using video, including writing, editing, and adapting scripts for live presentations, recorded video, and……
Advanced degree in a relevant scientific/clinical/regulatory field preferred. Ensures oversight of the development of the clinical documents (eg, Investigators'……
Bachelor's Degree in English, Technical Writing or related field required. Provides editorial skills in connection with all phases of the preparation and……
Creates communications strategy to showcase top technologies available for license. Required Education and Experience Bachelor’s Degree in a related field and……
Competency in the use of document management systems and review tools. Must have in-depth working knowledge of the relevant regulatory guidance (e.g. ICH, FDA,……
Experience developing documents using document management systems, collaborative authoring tools, and review tools. Plan and lead kickoff meetings.…
Read and review educational content with precision, keeping the science in training accurate and the clients’ stylistic preferences adhered to.…
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Spain – remote
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he Role:
We are searching for a quality-oriented, strategic thinking and fast paced Medical Writer to join our vibrant and dynamic startup team. This role will work across multiple accounts and therapeutic areas to deliver high quality scientific material that meets the needs and objectives of our clients. This role will work alongside designers and project managers to ensure complex concepts are translated into engaging and educational content within the given timeline and according to budget.
Key Responsibilities Include:
Review complex scientific information and translate it into engaging and educational messaging as per the needs of the client
Work cross-company to brainstorm, give feedback and share insights
Attend kick-off meetings with client to understand information and requirements. Take lead in communicating with clients for any follow up discussions or clarification
Liaise with clients to ensure the output meets their marketing objectives and is medically/scientifically accurate as well as engaging
Work alongside other medical writers to share expertise, edit and advise on content
Educate the organisation on medical and scientific terminology and concepts
Stay up to date on the pharmaceutical industry, recent research findings and treatments and provide insights for new business
Stay up to date on relevant clinical trials by reading and reviewing publications, attending courses and through membership in industry/professional associations. Provide reports and analysis on these trials and present to leadership on a regular basis
The right person for this role will have the following qualifications:
Background in medical and/or scientific research and advanced degree in a scientific discipline (preferably PhD)
Previous scientific and/or medical writing experience
Excellent knowledge of the scientific/medical industry and up to date knowledge of industry research, findings and key worldwide journal publications
An understanding of clinical trial processes with a thorough knowledge of associated regulatory guidelines
Strong organizational skills, attention to detail and ability to prioritize across multiple projects
Excellent written and spoken English language skills ( Level C2)
Excellent strategic communication skills with the ability to understand terminology, prioritize data and streamline and summarize complex concepts into a coherent and educational story
Strong editorial skills
Ability to think creatively and visualize information
Positive, ‘can do’ and team-oriented attitude
Ability to take initiative and make things happen independently and without supervision
Ability to work and communicate effectively with different personality types
Agile approach to work with the ability to move from one topic and/or project to the next quickly
Maturity to handle extremely confidential information
Location and Hours:
This is a full time, 40 hours per week role. The position can be remote (from home) in Porto Portugal or located in our office in Rotterdam, Netherlands.
Working with BlueNovius:
We are a fun and energetic team of dynamic and innovative professionals. We value continuous learning and love taking on new challenges. We pride ourselves on delivering cutting edge, innovative and top-quality products and services to our clients.
BlueNovius is a cutting edge digital marketing agency dedicated to serving the pharma and healthcare industry. Our clients trust us to deliver innovative and top-quality solutions that ensure healthcare professionals and patients stay informed and up to date on the best treatments available. To find out more, visit us at www.bluenovius.com.
To apply, please send us your CV along with a letter of motivation to recruitment.team@bluenovius.com .