An immediately available regulatory affairs specialist is required to cover a 12 month maternity leave working for a large pharmaceutical company based in Salisbury.
Reporting into an experienced regulatory affairs professional, you will be involved in preparing the relevant documentation for clinical trial applications in various different countries.
You will also be involved in the preparation of marketing authorisation applications and maintenance activities.
In order to be considered for this role you must be able to demonstrate the following:
· Immediately available
· Life-science degree
· Excellent attention to detail, be well-organised and able to deal with conflicting priorities
· Have previous experience in a regulatory affairs role working for global organisation
Due to the nature of the role, you will also be required to demonstrate excellent communication skills both oral and written.
Apply now for immediate consideration
Job Ref: 8739
More Info / Apply
Friday, 1 June 2012
Tuesday, 11 October 2011
Clinical Research Manager - Medical Devices - South East UK - to £50K
This innovative, university spin-out medical device company is looking to appoint a new Clinical Research Manager to manage six sites across Europe and Chile.
When you work for this company you become part of an small, highly dedicated, talented team of professionals, committed to quality and passionate about clinical research .
This is a site co-ordination role in which you will manage all site related activities from protocol review and feasibility through to close; covers five sites in Europe and one in Chile. Clinical studies will be focused on their cutting edge vascular medical devices.
You must have a significant experience working in the clinical research sector, with experience managing sites from initiation to closeout. Medical device experience is essential and a good understanding of catheterisation laboratory etiquette would be beneficial. You must have excellent attention to detail, experience of CRF completion and have good time management skills.
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 you will gain an attractive employment package with a competitive salary and the opportunity to join this fast moving company, highly farsighted company.
To discuss this role in more detail please contact Kristina on Kristina@seltekconsultants.co.uk
Job Ref: 8417
Friday, 12 August 2011
CRA or Senior CRA - Italy - Medical Devices - 8351
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
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
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
Wednesday, 20 July 2011
Manager, Clinical Support - Optometry - Europe - to €70K
This is a rare opportunity to join an innovative ophthalmic medical device company which is developing ground-breaking vision correction technologies for post-cataract surgery patients.
They are looking for an experienced optometry specialist to work with the ophthalmic surgeons throughout Europe and provide technical and application support on this innovative lens which is the only one of its kind on the market.
This position has arisen due to expansion throughout Europe, and you will be involved in working alongside the European team to ensure the surgeons are fully aware of the product's applications.
This lens has been twelve years in development. The company is now moving away from R&D and becoming more commercially active. Europe has a designated Sales Director who is involved in promoting this product throughout Europe, and a Director of Clinical Support who you will report to. You will act as a specialist in Europe for this lens, and be at hand to answer any technical queries regarding the application of this lens.
This company offers a small, friendly working environment. You can be home based anywhere in mainland Europe (in particular Germany, Spain, Italy, France or Czech Republic), and be expected to travel to visit the surgeons on a frequent basis.
The prospects are unlimited in this company, and the role will be what you make it! The company offers a strong support structure, but also the freedom for you to work independently.
So, if you are currently working in optometry, and would like the opportunity to work as a clinical support specialist, then please contact Kristina on Kristina@SeltekConsultants.co.uk for more detail.
Job Ref: 8294
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