
Services - Resourcing Solutions



		March 12 2010

Resourcing Solutions

UNDERSTANDING PEOPLE IS ONE OF OUR SPECIAL SKILLS

Years of recruiting talented people all over the world has led us to a unique position at Chiltern. We’ve come to understand the needs and aspirations of not only our sponsors but of pharmaceutical professionals themselves.

We continue to build a database of motivated and skilful people at all levels of experience in North America, Europe and Asia.

Using this resource and our own personnel, who are all given the opportunity to benefit from this additional experience, we regularly supply staff in a wide range of disciplines on a contract basis to the pharmaceutical industry around the world, often at extremely short notice.

In addition to short and long term contracts we can also offer senior personnel on an interim basis, and are able to assist with all your permanent resourcing needs.

We operate this service through our Resourcing Solutions team. If we can be of assistance or you would simply like further information please call us:

Europe
Tel: +44 1753 512000

North America
Tel: +1 770 929 3003

India
Tel: +91 22 4098 2700




		RefNo: SD-DSO-01 Job Title: DRUG SAFETY OFFICER - SLOUGH, BERKSHIRE - PERM WITH GLOBAL CRO Job Description: Due to our continuing growth Chiltern is looking to recruit an experienced Drug Safety Officer. The DSO will be responsible for wide variety of duties within our well established group. We will be flexible regarding experience and a structured training and development program will be put in place for the successful individual, however, it is imperative you have previous experience of working within Drug Safety in a CRO or Pharmaceutical Organisation in the UK. You must also have the relevant educational background in order to be considered. If successful you will work on a high profile 10,000 patient study to start with, however, there is other projects in mind for the future. We would like to bring someone on board to lead, for example setting up the project, liaise with the sponsor, travel abroad to train staff, problem solve issues, come up with a structured plan to aid the smooth running of processing the large number of SAE's. This is a hand’s on role so we will need someone who is happy to help process the SAE's as well as doing the lead tasks. It’s the perfect opportunity for someone wanting to gain career development and hands on project management experience. Chiltern is a leading International Clinical Research Organisation with offices across the World. Established in London in 1982, Chiltern International has accumulated extensive experience running clinical trials from Phase I to Phase IV across a broad therapeutic range. Chiltern provides an extensive range of services for both the international and national management of studies. Primary Duties: Attend study meetings Review pharmacovigilance aspects for studies Write or advise on pharmacovigilance sections for protocols and other documents Write and review SAE narratives and CIOMS forms for the pharmacovigilance department Provide 24 hour pharmacovigilance coverage for the pharmacovigilance group if contracted on projects on a rota system Discuss any issues arising from adverse events reported to pharmacovigilance both internally and with external clients Provide pharmacovigilance advice for Chiltern staff and medical department Be aware and advise on current pharmacovigilance legislation Participate in training sessions and workshops, including presenting reports from any conferences attended To perform training for other departments as appropriate Country or location: UK - London,UK - SouthEast



		Job Alert Service