Freelance lead Medical Writer
Posted a month ago
- London, Greater London
- Any
- External
- Expires In 2 months
Barrington James are exited to post a fantastic opportunity for one of our close clients. This company is a start up Pharma company that has exploded in size in recent years. They are looking for urgent leadership support within their Regulatory Writing writing team. This opportunity is perfect for someone who is ambitious, independent and wants to play a key role in working on the most innovative projects in the Pharmaceutical field.
In order to make an application, simply read through the following job description and make sure to attach relevant documents.
Requirements:
Masters degree or PhD in a related Science
Minimum experience of 9 years within the Pharmaceutical and Biotech space. With at least 7 years in Regulatory Writing
Extensive experience writing IB's (Investigator Brochures), CSR's (Clinical study reports), Protocols and Protocol amendments and CTD's working on a range of different modules
Previous experience of handling the development of junior Medical Writers
Clear, accurate and consistent style of writing having presented your work to a range of different audiences
Worked within Phases I-III
A range of Therapeutic area knowledge including Oncology, Immunology, Cardiology, Hematology and Neurology
Been freelancing for the last 5 years directly for Pharma and Biotech companies
This truly is an exiting opportunity for someone to join an ambitious company who are continuing to impress the market with their ground-breaking studies.
The opportunity has understandably been incredibly popular. We encourage all interested candidates to apply immediately as it is likely that recruitment will close prematurely.
By clicking "apply" you will be sending your CV to Charlie Denton at Barrington James. Charlie is a specialist Regulatory Writer recruiter and will discuss the opportunity in detail with you, facilitate your application and will manage the process acting as a link between the company and yourself.
Please call +44 12 93 77 66 44 if you have any questions, alternatively you can reach Charlie on #####.
In order to make an application, simply read through the following job description and make sure to attach relevant documents.
Requirements:
Masters degree or PhD in a related Science
Minimum experience of 9 years within the Pharmaceutical and Biotech space. With at least 7 years in Regulatory Writing
Extensive experience writing IB's (Investigator Brochures), CSR's (Clinical study reports), Protocols and Protocol amendments and CTD's working on a range of different modules
Previous experience of handling the development of junior Medical Writers
Clear, accurate and consistent style of writing having presented your work to a range of different audiences
Worked within Phases I-III
A range of Therapeutic area knowledge including Oncology, Immunology, Cardiology, Hematology and Neurology
Been freelancing for the last 5 years directly for Pharma and Biotech companies
This truly is an exiting opportunity for someone to join an ambitious company who are continuing to impress the market with their ground-breaking studies.
The opportunity has understandably been incredibly popular. We encourage all interested candidates to apply immediately as it is likely that recruitment will close prematurely.
By clicking "apply" you will be sending your CV to Charlie Denton at Barrington James. Charlie is a specialist Regulatory Writer recruiter and will discuss the opportunity in detail with you, facilitate your application and will manage the process acting as a link between the company and yourself.
Please call +44 12 93 77 66 44 if you have any questions, alternatively you can reach Charlie on #####.
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