Regulatory Medical Writer (CSR,Protocols, Submissions)

New Jersey  ‐ Onsite
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Keywords

Description

I am on the search for experienced Regulatory Medical Writers, who have a proven track record in Regulatory Medical Writing across a number of different regulatory documents. The therapeutic area is primarily Oncology, with the contract being on a 12 month rolling contract on a remote basis.

The successful Regulatory Medical Writer should have experience writing the following regulatory documents:

- Protocols

- Clinical Study Reports (CSR's)

- Submission Documents

- Summary Documents

- Individual Overviews

- Investigatory Brochures

I am looking for 7 years regulatory writing experience within pharma/biotech. Ideally educated at Masters Degree Level in life sciences, PharamD or MD preferred. If you are interested, please attach an up to date resume and I will be in touch.

To find out more about Real please visit www.realstaffing.com
Start date
01/2014
Duration
12 months
From
Real Staffing
Published at
04.01.2014
Project ID:
646270
Contract type
Freelance
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