PPD is a leading global contract research organization providing discovery, development and post-approval services as well as compound partnering programs. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 32 countries and more than 9,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a commitment to quality to help its clients and partners maximize returns on their R&D investments and accelerate the delivery of safe and effective therapeutics to patients
Post: Clinical Data Manager (CDM)
PPD is a leading global contract research organization providing drug discovery, development and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 44 countries and more than 11,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a commitment to quality to help clients and partners accelerate the delivery of safe and effective therapeutics and maximize the returns on their R&D investments. For more information, visit www.ppdi.com
You will primarily act as lead Clinical Data Manager across multiple projects, liaising with clients and colleagues in other functional groups through set up, maintenance and close out of projects. You should thrive in multi-national project teams and be focused on delivering exemplary levels of customer service. You will also have the opportunity to mentor more junior data management staff.
With experience of clinical trials, you will have in depth knowledge of FDA and ICH GCP requirements.
Strong organisational abilities are required for coordination of project deliverables, along with excellent communication and interpersonal skills, including the ability to negotiate.
Candidates with advanced experience may be considered for home based working.
Required Education and Experience
A minimum of three years data management experience.
Bachelor's or higher graduate degree in a science related field, licensed or certified health care training or equivalent experience
Valid driving license (where applicable)
Desired Education and Experience
Previous experience of managing studies
Previous experience in the CRO industry would be advantageous
Experience: Min. 3 Years
Location: Europe, Middle East & Africa - UK - Scotland - Bellshill - Fleming House 1
Education: BS, MS
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: CR
Job Code: 102100
End Date: 28th Sept., 2011
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