Associate Medical Writers

Brighton (UK), Fréjus (France)

Are you looking to start your career in medical writing?

Scinopsis is an experienced European medical writing agency specialised in producing clinical regulatory documentation and medical communications.

Due to continued growth, we are looking for entry-level Associate Medical Writers to join our English-speaking team in Brighton (UK) and Fréjus (South of France).

As an Associate Medical Writer, you will be responsible for developing high-quality clinical regulatory documents and medical communications for our clients in the pharmaceutical, biotechnology and medical device industries. You will have the opportunity to work on a variety of document types across a broad range of therapeutic areas.

This is a great opportunity to develop your skills as a medical writer within a supportive environment, at a company that prides itself on the high quality of its services. You will benefit from excellent in-house training and mentoring, as well as external training opportunities. We are a very friendly team, and staff happiness and work-life balance are a priority for us.

The role is ideal for someone with a strong scientific background and a natural ability to clearly communicate ideas through writing.

Responsibilities:

• Prepare and deliver a variety of clinical regulatory documents and medical communications
• Ensure that all projects are completed to a high level of quality, within budget and timelines
• Liaise with clients in a professional manner

Requirements:

• Life sciences or medical degree (BSc, MSc, PhD, PharmD or MD)
• Perfect written English and meticulous attention to detail
• Proven writing experience in an academic and/or professional setting
• Ability to interpret scientific and clinical data and write clear, concise and accurate text
• Excellent oral communication skills, flexible and friendly attitude
• Happy to work independently or as part of a team
• Ability to manage several different projects simultaneously and to meet tight deadlines
• Good computer skills (Microsoft Office 365)
• Willing to be office-based (ideally) but home-based applicants may be considered
• Willing to be employed (freelancers will not be considered)
• Legally entitled to work in the UK or France

Salary will depend on previous experience.

To apply, please send both your CV and cover letter in English, stating how you fulfil the above-listed job requirements, to jobs@scinopsis.com.

Medical Writers or Senior Medical Writers

Brighton (UK), Fréjus (France), Remote (UK, France, Germany or Portugal)

Are you an experienced medical writer looking for a new role with plenty of variety?

Scinopsis is an experienced European medical writing agency specialised in producing clinical regulatory documentation and medical communications.

We are looking for medical writers to join our English-speaking team in our offices in the UK (Brighton) or the South of France (Fréjus), or you could work remotely.

Please note that this position requires previous experience within the medical writing industry. If you do not have any previous experience, please consider the Associate Medical Writer position listed under Current Opportunities.

As a Medical Writer or Senior Medical Writer, you will be responsible for producing high-quality deliverables for our clients in the pharmaceutical, biotechnology and medical device industries. You will have the unique opportunity to work on a broad range of documents across a diverse array of therapeutic areas.

This is an exciting opportunity for a talented medical writer wishing to join a medical writing agency that prides itself on the high quality of its services. We are a very friendly team, and staff happiness and work-life balance are a priority for us.

All our writers benefit from continuous learning and professional development throughout their career at Scinopsis.

Responsibilities:

• Prepare and deliver a variety of clinical regulatory documents and medical communications
• Ensure that all projects are completed to a high level of quality, within budget and timelines
• Liaise with clients in a professional manner
• Supervise and mentor less experienced colleagues on medical writing projects (depending on experience)

Requirements:

• Life sciences or medical degree (MSc, PhD, PharmD or MD)
• Perfect written English and meticulous attention to detail
• Proven experience working on regulatory documents and/or medical communications
• Ability to interpret scientific and clinical data and write clear, concise and accurate text
• Ability to get up-to-speed in a new therapeutic area with ease
• Strong interpersonal skills with the ability to interact confidently with colleagues, clients, and external experts
• Flexible and friendly attitude
• Ability to manage several different projects simultaneously and to meet tight deadlines
• Good computer skills (Microsoft Office 365)
• Willing to be employed (freelancers will not be considered)
• Legally entitled to work in the UK or France/Germany/Portugal
• Appropriate and secure working environment for candidates wishing to work remotely

Salary will depend on previous experience.

To apply, please send both your CV and cover letter in English, stating how you fulfil the above-listed job requirements, to jobs@scinopsis.com.

Quality Control Specialist

Brighton (UK) or Remote (UK)

Scinopsis is a European medical writing agency specialised in producing clinical regulatory documentation and medical communications.

We are looking for an experienced Quality Control Specialist to perform quality control of clinical and regulatory documents, primarily in Microsoft Word (e.g. clinical study reports/protocols, CTD modules).

This role can be based at our office in Brighton or be fully home-based in the UK. We also have flexible working options with regards to hours and would consider a part-time position (no less than 3 days/week). We are a very friendly team, and staff happiness and work-life balance are a priority for us.

This is an exciting opportunity for a talented Quality Control Specialist wishing to join a medical writing agency that prides itself on the high quality of its services.

Responsibilities:

• Checking correct use of spelling, grammar and punctuation
• Checking accuracy of data in text and tables versus source documents
• Checking all aspects of document formatting versus document style guides/templates
• Checking consistency of content and formatting within and between documents
• Checking consistency of conclusions and claims versus source data
• Checking for consistent use of terminology, abbreviations and citations
• Checking functionality and consistency of presentation in PDF documents
• Communicating with document authors and clients during the quality control process

Requirements:

• A minimum of 2 years’ experience performing quality control of clinical/regulatory documents
• Excellent written English
• Meticulous attention to detail
• Highly methodical working style
• Proficient in Microsoft Word
• Good communication skills, flexible and friendly attitude
• Ability to support several different projects simultaneously and to meet tight deadlines
• Legally entitled to work in the UK
• Appropriate and secure working environment for candidates wishing to work remotely

Salary will depend on previous experience.

To apply, please send both your CV and cover letter in English, stating how you fulfil the above-listed job requirements, to jobs@scinopsis.com.

Freelance Medical Writers

Remote (UK or EU)

Scinopsis is an experienced European medical writing agency providing high-quality documents for the pharmaceutical, biotechnology and medical device industries.

We are looking for experienced freelance Medical Writers to support us with both short- and long-term project work. If you have immediate or upcoming availability, we would like to hear from you.

Responsibilities:

• Prepare and deliver clinical and regulatory documents (e.g. clinical study protocols/reports, CTD modules, investigator brochures, lay summaries) and/or scientific publications
• Ensure that all projects are completed to a high level of quality, within budget and timelines
• Liaise with Scinopsis team members and clients in a professional manner

Requirements:

• Extensive experience of developing clinical regulatory documents or publications within the medical writing industry
• Perfect written English and meticulous attention to detail
• Strong communication skills and impeccable project/time management skills
• Appropriate and secure working environment

To apply, please send both your CV and a summary of your experience to jobs@scinopsis.com.