Location: United Kingdom Frimley/Camberley
Closing Date: 24 Oct 16
Type: Full Time
Salary (£): On Application
Clinical Trial Administration Manager / GMO Support Manager, Novartis, UK Job Summary: Do you want to work for a Global Pharmaceutical company where you will get recognised for your hard work and commitment? Look no further, apply today. GMO Support Manager, Novartis, England. ...
Clinical Trial Administration Manager / GMO Support Manager, Novartis, UK
Do you want to work for a Global Pharmaceutical company where you will get recognised for your hard work and commitment? Look no further, apply today. GMO Support Manager, Novartis, England.
Novartis is currently recruiting for a Clinical Trial Administration Manager / GMO Support Manager to head up the Global Monitoring Operations Team!
** Global Monitoring Operations / Clinical Trials / compliance / CTA Manager / Clinical Trial Assistant / GMO **
The purpose of the Clinical Trial Administration Manager / GMO Support Manager role is to lead and manage the GMO Support Team and be part of the GMO Leadership team. The GMO Support Manager provides a professional, key support function across multi-disciplinary teams for regulatory, ethics, financial and archiving activities of all GMO clinical trials within the UK and Ireland in accordance with GCP/IGCH, international (FDA, EMA) and local regulations.
•Core member of the GMO Leadership Team, providing leadership to the GMO Support Team
•Ensures that GMO is provided with a professional, efficient and key support service
•Supports GMO Country Head with Leadership Team initiatives and works closely with other GMO Leadership Team members to ensure clinical studies are set up and executed within required timelines to Novartis SOP standards
•Leads, develops and manages Site Management Specialists, Finance Associates, Clinical Archivists and Contracts Manager
•Selects, recruits and retains high calibre staff within defined budget.
•Sets team and individual objectives, reviews progress, manages and mentors direct line reports.
•Ensures AQWA, the Novartis Quality database, is updated with any process deviations and incidents
•Oversees the management of the investigator clinical trial payment system on behalf of GMO.
•Ensures that payments are processed accurately and in a timely manner.
•Assists Project Managers in running of clinical studies and supports field based CRA team to maximise study performance.
Our mission is to care and cure; We want to discover, develop and successfully market innovative products to prevent and cure diseases, to ease suffering and to enhance the quality of life. We also want to provide a shareholder return that reflects outstanding performance and to adequately reward those who invest their money, their time and their ideas in our company.
Benefits of Working for Novartis:
Strong Work/Life Balance, flexible working
Top UK Employer
Comprehensive Medical Insurance
Employee Recognition Scheme
Sports & Social Club
‘I came for the job, I stay for the culture’
#LI-P Minimum requirements The ideal candidate will have:
•A degree in a scientific/ health care discipline or equivalent relevant experience
•Significant relevant experience within the clinical Research environment with an excellent knowledge of Clinical Research processes including ICH GCP
•Previous experience as a senior CRA/ Project Manager
•Previous line management, coaching and mentoring experience
•Experience in UK ethics / R&D requirements
•Strong financial management and negotiation skills
Novartis are an equal opportunities employer and welcome applications from all suitably qualified persons
Novartis Pharmaceuticals UK Limited
Frimley Business Park
|Tel:||+44 (0)1276 692255|
|Fax:||+44 (0)1276 692508|
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