Company: i-Pharm Consulting
Closing Date: 02 Dec 16
Salary (£): Negotiable
Principal Medical Writer, Global CRO - Home-basedPrincipal Medical Writer required for a global Clinical Research Organisation. You will be responsible for a variety of clinical documents for a wide range of both international and local sponsors across all therapeutic areas. This position can be home-based anywhere in Europe but you must be eligible to work in the EU. ...
Principal Medical Writer, Global CRO - Home-based
Principal Medical Writer required for a global Clinical Research Organisation. You will be responsible for a variety of clinical documents for a wide range of both international and local sponsors across all therapeutic areas. This position can be home-based anywhere in Europe but you must be eligible to work in the EU.
Principal Medical Writer
Competitive salary and benefits package
Excellent on-going career development opportunities
Write clinical documents for submission to regulatory authorities, including briefing documents, clinical development plans, previous human experience summaries, human pharmacology summaries, investigator brochures, study protocols, model informed consents, interim and final clinical study reports, common technical document (CTD) clinical overviews and summaries, safety update/aggregate reports, integrated summaries of safety and efficacy.
- Experience in writing multiple clinical study reports, and either CTD documents or study protocols.
-Experience with a variety of documents (CSRs, IBs, protocol/amendments, briefing books, HA responses, post-submission safety updates, and preferably submissions [clinical CTD modules].
- Degree in science or health related discipline
- Excellent communication skills
-Educated to degree level in Life Sciences/Health Related Sciences or equivalent.
ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
If you would like to discuss this vacancy further, please call Principal Consultant Niall Behan on +44 (0)20 3189 0463, or email firstname.lastname@example.org. If this role is not suitable, Niall is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
Senior Medical Writer / Medical Writer / UK / England / Scotland / London / CRO / Senior Medical Writer / Project Management / Clinical Research / Medical Writer / Europe / France / Spain / Protocol
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