Medical Writer Life Science
hace 6 días
Spain - remote
**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.
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