Thursday 23 December 2010

Senior Compliance Associate - Clinical Research - London - to £39K

One of the leading global CROs is looking to recruit a Senior Compliance Associate to join their offices in the UK.
It's a rare opportunity in QA for someone who wants to acquire the experience required to become a QA Manager in the near future
You will be responsible for GCP audits, QA reviews and evaluations and writing of SOPs. You will also provide training to clinical research staff on GCP regulations.
You will be required to provide input and assistance to Business Development for time and cost proposal development and provide project management oversight for compliance-related tasks and programs
To be successful in this role you must have experience in a similar position in clinical research, regulatory affairs or a relevant healthcare research position. You must have relevant GLP audit work experience ideally gained in a CRO and strong working experience of GLP, GMP and GCP Audits
You will be required to travel up to 40% of the time, and have the motivation and drive to work independently.

Job Ref: 8061

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Thursday 16 December 2010

Clinical Study Leader / Junior Project Manager - East Anglia

This UK based pharmaceutical company is looking to recruit a Clinical Study Leader/Junior Project Manager, who will take responsibility for the management of phase III oncology and cancer pain studies. This is an excellent opportunity for a Senior CRA to step up into project management.

You will work within a dynamic leading edge research environment, providing scientific input and project management to clinical trials, as well as being responsible for communicating budgetary and financial aspects of studies.

You will need to be educated to at least BSc/RGN level, with considerable experience of monitoring. Involement in project management duties will be an advantage. Experience in Phase III clinical study management with experience in oncology or pain management would be beneficial
You must be a self-starter, comfortable working independently and able to make decisions.

In return for your experience, you will be given a competitive remuneration package and a chance to work in this expanding, dynamic company.

For more information, or if you would like to apply, please email kristina@seltekconsultants.co.uk or call Kristina on 01279 657716

Job Ref: 8047

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Wednesday 8 December 2010

Clinical Project Manager - Late Phase - Home Based, Europe - to £54K

This leading, global clinical research organisation (CRO) is looking to recruit a Project Manager to manage various late phase clinical research projects throughout Europe. This position has arisen due to expansion, as they have recently won a large number of late phase proposals and are looking for someone to take control of the projects.

This is an expanding, dynamic CRO that has tripled in size in Europe over the last three years. Specialising in the development of oncology, CNS, anti-infective and cardiovascular products they offer a comprehensive range of services to small and medium sized biotech and pharmaceutical companies. This company focuses on its people, offering excellent training and development opportunities and a fun, team focused working environment.

You will lead the clinical team to ensure on-time, on-budget performance, review and approve regulatory and administrative documents from investigator sites, as well as reviewing CRF s and SAE reports.

You will also plan, coordinate, and present at investigators meetings, participate in proposal meetings with potential clients as well as prepare project management reports for clients, project personnel, and the company s management team.

You must be educated to BSc level or RGN, and have a successful background in managing late phase international projects. You can be based in almost any European country.

To discuss this role in confidence, please call Kristina on 01279 657716 or email kristina@seltekconsultants.co.uk

Job Ref: 8037

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Clinical Project Manager - CNS - Home Based, Europe - to £54K

This leading, global clinical research organisation (CRO) is looking to recruit a Project Manager to manage various CNS clinical research projects throughout Europe. This position has arisen due to expansion, as they have recently won a large number of CNS proposals and are looking for someone to take control of the projects.

This is an expanding, dynamic CRO that has tripled in size in Europe over the last three years. Specialising in the development of oncology, CNS, anti-infective and cardiovascular products they offer a comprehensive range of services to small and medium sized biotech and pharmaceutical companies. This company focuses on its people, offering excellent training and development opportunities and a fun, team focused working environment.

You will lead the clinical team to ensure on-time, on-budget performance, review and approve regulatory and administrative documents from investigator sites, as well as reviewing CRF s and SAE reports.

You will also plan, coordinate, and present at investigators meetings, participate in proposal meetings with potential clients as well as prepare project management reports for clients, project personnel, and the company s management team.

You must be educated to BSc level or RGN, and have a successful background in managing international projects. You can be based in almost any European country.

To discuss this role in confidence, please call Kristina on 01279 657716 or email kristina@seltekconsultants.co.uk

Job Ref: 8036

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Junior Project Manager - Phase I / IIa Clinical Studies - UK - to £45K

This UK based pharmaceutical company is looking to recruit a Junior Project Manager, who will take responsibility for the management of early phase (Phase I / IIa and Investigator Initiated) clinical studies. This is an excellent opportunity for a SrCRA to step up into project management.

You will work within a dynamic leading edge research environment, to provide scientific input and project management to clinical trials, as well as being responsible for communicating budgetary and financial aspects of studies.

You will need to be educated to at least BSc/RGN level, with considerable experience of monitoring. Involement in project management duties will be an advantage. Experience in Phase I / IIa clinical study management would also be beneficial
You must be a self-starter, comfortable working independently and able to make decisions.

In return for your experience, you will be given a competitive remuneration package and a chance to work in this expanding, dynamic company.

For more information, or if you would like to apply, please email kristina@seltekconsultants.co.uk or call Kristina on 01279 657716

Job Ref: 8001

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Friday 3 December 2010

Senior CRA / CRA II - Bulgaria - to €36k

This sophisticated and innovative global clinical research organisation (CRO) is looking to recruit a Clinical Research Associate (CRA II) and Senior Clinical Research Associate (Senior CRA) in Bulgaria. This company prides itself in being scientifically strong with powerful scientific backing. They also have great expertise in the drug development process but focus mainly on CNS, cardiovascular and inflammatory areas.

This CRO has a lower than average staff turnover, and also has an in-depth training system in place which means excellent career development opportunities for you!

If you are an experienced monitor looking for the next step up in this global, expanding and dynamic company, then please apply or email Kristina@seltekconsultants.co.uk.

Job ref: 8031

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Извинявам се за превода Google

Този изтънчен и иновативни световната клинична изследователска организация търси да назначи клинична научен сътрудник и старши научен сътрудник Клинична в България. Тази фирма се гордее с научно е силна с мощна научна основа. Те също имат голям опит в процеса на разработване на лекарства, но се съсредоточи главно върху ЦНС, сърдечно-съдови и възпалителни райони.

Този клиничен научноизследователска организация е по-ниско от средното текучество на персонал, и освен това има задълбочена система за обучение на място, което означава, отлични възможности за професионално развитие за вас!

Ако сте опитен наблюдава търсят следващата стъпка в тази глобална, разширяване и динамична компания, моля прилага или имейл Kristina@seltekconsultants.co.uk.