Freelance Medical Writer

Location
England
Salary
Negotiable
Posted
21 Nov 2018
Closes
19 Dec 2018
Ref
342593/004
Contract Type
Contract
***A Global CRO in the UK is looking for 2X Freelance Medical Writers to take part in a 6-12 Month Project***


Responsibilities:

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FDA Briefing Documents
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Clinical Study Reports (CSRs)
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Investigational New Drug (INDs)
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Clinical Study Protocols and Amendments
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Investigator Brochures (IBs)
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IND Annual Reports/ DSURs
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Patient Informed Consent Forms (PICFs)
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Executive Summaries for Efficacy or Safety



Skills and Experience Required

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At least 4 years of Medical Writing Experience within a pharmaceutical or related background
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Working experience in drug safety, EU and international regulatory guidelines, drug development, biostatistics, pharmacology, clinical trial methodology and oncology
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Ability to work independently
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Familiarity with eCTD format
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Previous oncology writing experience
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Bachelor’s degree required / Advanced degree preferred
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Ability to travel if required.



What this Job Offers You

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6 Month Contract minimum
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Flexibility (fulltime-Part-time)

How to apply

Apply here if you are interested in this opportunity or if you would like a confidential discussion about your career opportunities please contact or phone +442037588916.



Only candidates with the right to work in the EU or a full valid visa will be considered.

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