Company: i-Pharm Consulting
Closing Date: 04 Nov 16
Salary (£): Negotiable
Medical Writing Manager – Global CROMy client a top 5 CRO is looking for a Medical Writing Manager (Phase I-IV) to lead the preparation of clinical trials and other medical writing projects across all phases. This position can be offered fully home -based.What you will be doing:• Be the Lead author of clinical documents for inclusion in submission dossiers and coordinating clinical responses to regulatory authority questions. ...
Medical Writing Manager – Global CRO
My client a top 5 CRO is looking for a Medical Writing Manager (Phase I-IV) to lead the preparation of clinical trials and other medical writing projects across all phases. This position can be offered fully home -based.
What you will be doing:
• Be the Lead author of clinical documents for inclusion in submission dossiers and coordinating clinical responses to regulatory authority questions.
• Being the lead for the preparation of documents for clinical trials (phases I-IV) across a range of therapeutic areas.
• Management of medical writing projects
• May mentor junior staff.
1. A life science degree and many years’ experience within Medical Writing as a lead writer.
2. Robust experience in regulatory medical writing
3. Strong project management experience
If you would like to discuss this vacancy further, please call Regulatory Team Leader Niall Behan on +44 (0)20 3189 2297, 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.
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.
Pharmaceutical, Biotech, Biotechnology, Biochemistry, CRO, Pharma, Pharmaceutical, Clinical, Clinical Regulatory Affairs, Regulatory Affairs Manager, Regulatory Affairs Senior Manager, Senior Regulatory Affairs Manager, Regulatory Affairs Management, Reg Affairs, Reg Affairs Manager, Regulatory Affairs Coordinator, Regulatory Affairs Consultant, Principal Consultant, Principal Regulatory Consultant, Regulatory Affairs Associate, Regulatory Affairs Officer, Regulatory Affairs Expert, Regulatory Affairs Specialist, Regulatory Affairs Executive Associate, Submissions, GRA, RA, Regulatory Affairs Submissions Associate, Regulatory Affairs Submissions Coordinator, RA Submissions Coordinator, Senior Regulatory Affairs Associate, Regulatory Submissions, Regulatory, Regulatory Affairs Associate, Regulatory Affairs Associate II, Regulatory Line Management, Oncology, cardiovascular, vaccines, general medicines, CNS, Respiratory, England, UK
PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.