Study Manager Contract Role One of the largest Pharmaceutical Company is offering a fantastic opportunity for an experienced Project Manager to join a dynamic team based in Basingstoke. Key Responsibilities: As a Study Manager you will be required to lead the study team to design, develop and deliver the clinical study.
Marketing Manager Laverstoke, Hampshire £ 25000 - £ 32000 + bonus - depending on experience Our client is a dynamic B2B marketing agency specialising in 'Point of Contact' solutions. By offering marketing services in the often over-looked media of audio, video and fragrancing, we help companies create great first impressions.
Responsible for the planning, implementation, execution and management of clinical research study/studies and/or programs. Manages clinical outsourcing to CROs or other clinical vendors such as labs, IRBs, etc and oversees the financial and budgetary aspects of the study/studies Authors/oversees protocols, informed consent forms, sections of investigational drug brochures, study report writing and integrated summaries for regulatory submissions.
Posting Title Sr Clinical Scientist Depression Job ID 2674BR Function Specialty Pharma Division Research and Development Employee Type Regular Search Location(s) United Kingdom - Basingstoke Job Category Clinical Development Operations Job Description Leads the study team to design, develop and deliver the clinical study; Authors protocols, ICFs and study related plans developed by Shire.
Primary Role Providing leadership and management within CDMA to provide medical and scientific support for products within assigned therapy area. Medical & Clinical strategy for Shire products. Oversight of study design and data generated from Shire sponsored Phase I-IV clinical research programs ensuring that regulatory authority requirements, stakeholder requirements, and quality standards are met.
Responsible for the planning, implementation, execution and management of clinical research study/studies and/or programs. Manages clinical outsourcing to CROs or other clinical vendors such as labs, IRBs, etc and oversees the financial and budgetary aspects of the study/studies Authors/oversees protocols, informed consent forms, sections of investigational drug brochures, study report writing and integrated summaries for regulatory submissions.
Posting Title Sr Clinical Scientist Depression Job ID 2674 Function Specialty Pharma Division Research and Development Employee Type Regular Search Location(s) United Kingdom Basingstoke Job Category Clinical Development Operations Job Description Leads the study team to design, develop and deliver the clinical study; Authors protocols, ICFs and study related plans developed by Shire.
Primary Role Providing leadership and management within CDMA to provide medical and scientific support for products within assigned therapy area. Medical & Clinical strategy for Shire products. Oversight of study design and data generated from Shire sponsored Phase I IV clinical research programs ensuring that regulatory authority requirements, stakeholder requirements, and quality standards are met.
Michael Page Life Sciences is recruiting for a Basingstoke based Pharmaceutical business who are looking for a Clinical Document Management Specialist to join the team. The Clinical Document Management Specialist position reports to the Clinical Document Manager and will act as advisor/mentor to the Specialists in the UK team ensuring timelines are met and assisting in resolving technical problems.
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