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Skills
Freelance Medical Writer - Oct 2013 to present
I am happy to provide you with the following professional medical writing services and welcome requests for proposals from pharmaceutical, biotechnology and medical device companies in addition to clinical research organisations. I am open to all types of medical writing requests.
- Writing scientific documents in accordance with relevant templates, guidelines and procedures
- Quality control and peer review of scientific documents
- Liaising with client teams to discuss exact project requirements, develop timeline plans for writing and review of documents, and delivery of documents in accordance with agreed timelines.
Member of EMWA (European Medical Writer’s Association)
My document experience includes:
? Protocols
? Clinical Study Reports
? Patient Safety Narratives
? Risk Management Plans
? Annual Safety Reports
? Periodic Safety Update Reports
My therapeutic area experience includes:
? Oncology
? Cardiovascular Disorders
? Central Nervous System Disorders
? Endocrinology
? Gastrointestinal Disorders
? Infectious Diseases
? Immunology
? Musculoskeletal Disorders
ICON CLINICAL RESEARCH
Principal Medical Writer - Mar 2004 to Sep 2013
As Principal Medical Writer, I was principal operational contact between ICON Medical Writing and both internal and external clients to ensure correct conduct of ongoing projects and effective representation of the department\\\'s capabilities for potential projects. In addition, I was responsible for provision of scientific and technical guidance to the writing team; interaction with clients regarding scientific and technical aspects of projects; participation in new business activities; participation in external and internal audits; and the development of new writing services. Importantly, I spent at least 50% and up to 90% of my time actively writing and reviewing regulatory documentation for assigned medical writing projects.
GSK
Quality Assurance Laboratory Analyst Oct 2001 to Feb 2004
- QA analysis of respiratory drug samples using various methods including HPLC, UV and IR.
- Analysis, write-up and review of laboratory data.
- Write-up and review of laboratory investigation reports.
- Validation of laboratory equipment.
H.W. Wilson Company
Abstract Writer and Editor - Aug 1998 to Apr 2000
Writer and editor of applied science and technology abstracts for publication on CD Rom.
I am happy to provide you with the following professional medical writing services and welcome requests for proposals from pharmaceutical, biotechnology and medical device companies in addition to clinical research organisations. I am open to all types of medical writing requests.
- Writing scientific documents in accordance with relevant templates, guidelines and procedures
- Quality control and peer review of scientific documents
- Liaising with client teams to discuss exact project requirements, develop timeline plans for writing and review of documents, and delivery of documents in accordance with agreed timelines.
Member of EMWA (European Medical Writer’s Association)
My document experience includes:
? Protocols
? Clinical Study Reports
? Patient Safety Narratives
? Risk Management Plans
? Annual Safety Reports
? Periodic Safety Update Reports
My therapeutic area experience includes:
? Oncology
? Cardiovascular Disorders
? Central Nervous System Disorders
? Endocrinology
? Gastrointestinal Disorders
? Infectious Diseases
? Immunology
? Musculoskeletal Disorders
ICON CLINICAL RESEARCH
Principal Medical Writer - Mar 2004 to Sep 2013
As Principal Medical Writer, I was principal operational contact between ICON Medical Writing and both internal and external clients to ensure correct conduct of ongoing projects and effective representation of the department\\\'s capabilities for potential projects. In addition, I was responsible for provision of scientific and technical guidance to the writing team; interaction with clients regarding scientific and technical aspects of projects; participation in new business activities; participation in external and internal audits; and the development of new writing services. Importantly, I spent at least 50% and up to 90% of my time actively writing and reviewing regulatory documentation for assigned medical writing projects.
GSK
Quality Assurance Laboratory Analyst Oct 2001 to Feb 2004
- QA analysis of respiratory drug samples using various methods including HPLC, UV and IR.
- Analysis, write-up and review of laboratory data.
- Write-up and review of laboratory investigation reports.
- Validation of laboratory equipment.
H.W. Wilson Company
Abstract Writer and Editor - Aug 1998 to Apr 2000
Writer and editor of applied science and technology abstracts for publication on CD Rom.
Project history
References available on request.
Local Availability
Open to travel worldwide
I work from home in Ireland but am available to travel to meet clients across Europe, US and Rest of World as needed.
Other
I am a highly-experienced medical writer with the ability to convey complex scientific information in a clear and concise manner in accordance with templates, guidelines and procedures in order to deliver documents that meet specific client expectations as well as regulatory requirements. I work in a proactive, efficient and timely manner to deliver excellent quality work on time and within budget. I have an open, friendly approach and believe good communication is essential throughout all projects. I am very used to working with multidisciplinary teams consisting of project managers, statisticians, medical monitors, regulatory experts and quality personnel. I am open to all types of writing opportunities.
