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| Van Wyk, Illona |
| Templestowe, Vic |
| Tel: 0405 463 996 |
| Email: illona.vanwyk@gmail.com |
| Skills and services |
| I have approximately 14 years experience in various roles in clinical research. The last 8 years I have been a medical writer with experience in Phase I to IV clinical trials. I can write protocols, informed consent documents, annual safety reports (ASRs), periodic safety update reports (PSURs), Investigator’s Brochures, patient narratives and clinical study reports (CSRs). Most of my experience is in CSRs. So, if you need a CSR written according to ICH E3 to report your trial results I can do it in a timely manner and it would be of excellent quality. |
| Subjects |
I can write and review all documents needed in clinical research, especially clinical study reports.
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I can also assist with writing and reviewing SOPs or any other documents relating to clinical research, including CRFs, marketing materials, newsletters, etc. I can also assist in the data management of smaller trials and/or using electronic CRFs. |
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