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……
CMEsquared® accredited education is developed based on a thorough assessment of identified educational needs, resulting in timely, relevant learning……
Amiculum is an independent agency that delivers communications and consultancy services to pharmaceutical, biotechnology and health technology companies across……
Informed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research……
Read and review educational content with precision, keeping the science in training accurate and the clients’ stylistic preferences adhered to.…
The Technical Writer/Editor develops clear, accurate, and accessible content that translates scientific evidence, clinical protocols, and technical information……
This varied role involves writing accurate scientific / commercial copy for a range of printed and computer-based scientific materials from technical……
Contributes to technical proposals and responds to technical questions. Prepares scientific and regulatory documents on behalf of government and private sector……
Develop, write, and edit a wide range of clinical, scientific, and research-based documents, including study protocols, leadership reports, manuscripts for……
The ideal candidate will have an advanced degree in a life-sciences field, meticulous attention to detail and the ability to simultaneously work on multiple……
Positions are available for those looking for an entry-level role in the field as well as those with some prior experience. Role Type: Full-time, permanent.…
An advanced science or clinical degree (eg, PhD, MBBS, MD, PharmD, RN, RPh) or a lesser degree with significant relevant experience is required.…
Leads client meetings when appropriate, including project kick-off, regular status, and ad hoc client and healthcare professional (HCP) calls; updates clients……
Our Scientific team partners with global pharmaceutical and biotechnology companies to develop scientifically rigorous, strategically aligned, and compliant……
Provide mentorship, guidance and advice for entry-level writers, as required. Contribute to project tracking and reporting using relevant tools (e.g. DataVision……
Bachelor’s degree in a scientific or clinical discipline or related field is required; Ph.D. preferred. Author and project manage SME contribution to develop……
Advanced degree in a scientific or healthcare‑related field preferred (eg, MSc, PhD, PharmD, MD). Serve as principal scientific contact for client stakeholders……
Participate in client calls/correspondence relating to content approval; record and clarify all content change requests and ensure relevant information is……
Advanced degree in a scientific or healthcare‑related field preferred (eg, MSc, PhD, PharmD, MD). Serve as one of the principal scientific contacts for client……
Advanced degree in a scientific or healthcare‑related field preferred (eg, MSc, PhD, PharmD, MD). Serve as one of the principal scientific contacts for client……
Participate in client calls/correspondence relating to content approval; record and clarify all content change requests and ensure relevant information is……
As assigned, develop relationships and collaborate closely with clients and key opinion leaders to develop scientific content and execute medical communication……
2-4 years in medical communications, healthcare agency, medical education, or similar field. Ensuring project quality and outcomes by demonstrating in depth……
Ability to independently formulate key messages from clinical study data. Planning, writing, editing, formatting, and QC review of timely and high-quality……
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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 .