The medical devices arm of this global CRO is looking to recruit a senior CRA in Italy.
When you work for this company you become part of an expanding, talented team of professionals, committed to quality and passionate about clinical research! This is site co-ordination role in which you will manage all site related activities from protocol review and feasibility through to close out locally in Italy. Clinical studies will be focused on their medical devices.
Additional responsibilities will include mentoring/coaching junior CRAs, local project management activities and some international liaising at site level - there will also be the chance to take on lead duties within specific projects. This is an excellent opportunity to work for a medium sized CRO that places their employees career progression as their number one priority!
You will have a scientific background and proven track record of start up, initiation, monitoring and close out activities in Italy. You will be able to work as part of a small team as well as independently with minimal supervision. Flexibility to travel is essential in this role. In return for your experience is a competitive remuneration package and the opportunity to work with a highly experienced and fun team!
To discuss this role in more detail, please contact Kristina on kristina@seltekconsultants.co.uk
Click here to apply
Clinical Research Jobs is a specialist division of Seltek Consultants. The clinical research division works closely with leading pharmaceutical and biotech companies as well as CROs to source high calibre candidates across a broad range of disciplines - from entry to director level. Vacancies will be posted here as we receive them along with news and information from the industry.
Friday 12 August 2011
CRA or Senior CRA - Spain - Medical Devices - 8350
The medical devices arm of this global CRO is looking to recruit a senior CRA in Spain .
When you work for this company you become part of an expanding, talented team of professionals, committed to quality and passionate about clinical research! This is site co-ordination role in which you will manage all site related activities from protocol review and feasibility through to close out locally in Spain. Clinical studies will be focused on their medical devices.
Additional responsibilities will include mentoring/coaching junior CRAs, local project management activities and some international liaising at site level - there will also be the chance to take on lead duties within specific projects. This is an excellent opportunity to work for a medium sized CRO that places their employees career progression as their number one priority!
You will have a scientific background and proven track record of start up, initiation, monitoring and close out activities in Spain. You will be able to work as part of a small team as well as independently with minimal supervision. Flexibility to travel is essential in this role. In return for your experience is a competitive remuneration package and the opportunity to work with a highly experienced and fun team!
To discuss this role in more detail, please contact Kristina on kristina@seltekconsultants.co.uk
Click here to apply
When you work for this company you become part of an expanding, talented team of professionals, committed to quality and passionate about clinical research! This is site co-ordination role in which you will manage all site related activities from protocol review and feasibility through to close out locally in Spain. Clinical studies will be focused on their medical devices.
Additional responsibilities will include mentoring/coaching junior CRAs, local project management activities and some international liaising at site level - there will also be the chance to take on lead duties within specific projects. This is an excellent opportunity to work for a medium sized CRO that places their employees career progression as their number one priority!
You will have a scientific background and proven track record of start up, initiation, monitoring and close out activities in Spain. You will be able to work as part of a small team as well as independently with minimal supervision. Flexibility to travel is essential in this role. In return for your experience is a competitive remuneration package and the opportunity to work with a highly experienced and fun team!
To discuss this role in more detail, please contact Kristina on kristina@seltekconsultants.co.uk
Click here to apply
CRA or Senior CRA - France - Medical Devices - 8349
The medical devices arm of this global CRO is looking to recruit a senior CRA in France.
When you work for this company you become part of an expanding, talented team of professionals, committed to quality and passionate about clinical research! This is site co-ordination role in which you will manage all site related activities from protocol review and feasibility through to close out locally in France. Clinical studies will be focused on their medical devices.
Additional responsibilities will include mentoring/coaching junior CRAs, local project management activities and some international liaising at site level - there will also be the chance to take on lead duties within specific projects. This is an excellent opportunity to work for a medium sized CRO that places their employees career progression as their number one priority!
You will have a scientific background and proven track record of start up, initiation, monitoring and close out activities in France. You will be able to work as part of a small team as well as independently with minimal supervision. Flexibility to travel is essential in this role. In return for your experience is a competitive remuneration package and the opportunity to work with a highly experienced and fun team!
To discuss this role in more detail, please contact Kristina on kristina@seltekconsultants.co.uk
Click here to apply
When you work for this company you become part of an expanding, talented team of professionals, committed to quality and passionate about clinical research! This is site co-ordination role in which you will manage all site related activities from protocol review and feasibility through to close out locally in France. Clinical studies will be focused on their medical devices.
Additional responsibilities will include mentoring/coaching junior CRAs, local project management activities and some international liaising at site level - there will also be the chance to take on lead duties within specific projects. This is an excellent opportunity to work for a medium sized CRO that places their employees career progression as their number one priority!
You will have a scientific background and proven track record of start up, initiation, monitoring and close out activities in France. You will be able to work as part of a small team as well as independently with minimal supervision. Flexibility to travel is essential in this role. In return for your experience is a competitive remuneration package and the opportunity to work with a highly experienced and fun team!
To discuss this role in more detail, please contact Kristina on kristina@seltekconsultants.co.uk
Click here to apply
CRA or CRA II - Hungary - 8347
An exciting opportunity has arisen in this leading CRO for a CRA role with clinical responsibility for Hungary!
You will be responsible for leading a team of experienced CRAs across a range of high profile oncology projects! When you work for this medium sized, well respected company you work for a company specialising in supporting the development of new drugs in a wide range of therapeutic areas: oncology in particular, as well as CNS and cardiovascular sciences.
With an international presence and high profile pharmaceutical and biotechnology clients, the company offers an excellent environment in which to develop your career further. In this role you will be responsible for clinical study sites based in Hungary from initial start up through to close out across phase II and III projects with an international scope. Within these projects you will be responsible for all site management and core monitoring activities, site specific training, clinical site budgets and management of site level relationships. This company offers excellent training and development to its CRAs, both internally and externally, along with ongoing performance monitoring to help you develop your career, either into clinical management or project management, with the company.
Who are we looking for? You will be an experienced CRA able to demonstrate the ability to manage all aspects of site activity from set up through to close-out in Hungary. Experience in the monitoring of oncology studies is essential. On offer is a competitive renumeration package, excellent training and development, and the opportunity to become part of a talented international team!
For more information or to register your interest please contact Kristina on kristina@seltekconsultants.co.uk
Please note that by applying to this role, you are only expressing your interest; I will discuss the role and company in detail with you before your CV is submitted to our client.
Click here to apply
You will be responsible for leading a team of experienced CRAs across a range of high profile oncology projects! When you work for this medium sized, well respected company you work for a company specialising in supporting the development of new drugs in a wide range of therapeutic areas: oncology in particular, as well as CNS and cardiovascular sciences.
With an international presence and high profile pharmaceutical and biotechnology clients, the company offers an excellent environment in which to develop your career further. In this role you will be responsible for clinical study sites based in Hungary from initial start up through to close out across phase II and III projects with an international scope. Within these projects you will be responsible for all site management and core monitoring activities, site specific training, clinical site budgets and management of site level relationships. This company offers excellent training and development to its CRAs, both internally and externally, along with ongoing performance monitoring to help you develop your career, either into clinical management or project management, with the company.
Who are we looking for? You will be an experienced CRA able to demonstrate the ability to manage all aspects of site activity from set up through to close-out in Hungary. Experience in the monitoring of oncology studies is essential. On offer is a competitive renumeration package, excellent training and development, and the opportunity to become part of a talented international team!
For more information or to register your interest please contact Kristina on kristina@seltekconsultants.co.uk
Please note that by applying to this role, you are only expressing your interest; I will discuss the role and company in detail with you before your CV is submitted to our client.
Click here to apply
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