Thursday, August 24, 2006
Medical writer required, responsible for production of protocols, case report forms, clinical study reports and documents for Phase I – IV clinical trials. Company provides fully comprehensive laboratory research, product development and clinical services with international focus, uniquely designed to meet needs of clients in rapidly evolving and demanding environment. Experience in writing, abstracting, editing and publishing, an understanding of statistics, clinical research or hospital experience, computer skills including windows driven word processing packages and knowledge of Biology / Physiology. Excellent written communication and organisation skills, good eye for detail, teamwork and flexibility. BSc in life sciences or nursing qualification. Produce case report forms Quality control for other medical writers work and patient safety narratives basis for inclusion of clinical study reports. Liaise with departments and clients under instruction of relevant project and internal line management. Meet SOP’s and relevant quidelines including International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH). Represent medical writing at project meetings, attend meetings and training sessions, maintain accurate records, become familiar with current regulatory guidelines, software packages and markets requirements and assist in development, implementation and update of Standard Operating Procedures (SOP’s).
Call Lynn Beaty on +44 (0)1628 418151or email firstname.lastname@example.org