Wednesday, 6 June 2012

Regulatory Affairs

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

Pharmacovigilence Associate - South East UK - to £25K

An exciting pharmaceuticals company in Cambridge is looking to hire a Pharmacovigilance Associate to join their team on a permanent basis.
The company is currently involved in some interesting research into alternative therapies for unmet medical needs and as such requires and enthusiastic and dedicated individual to join their team.
You will be working on a global level ensuring the safety of these therapies in both clinical trials and post-marketing settings.
Following an impressive training programme, you will be responsible for the following:
· Data entry, review and assessment of adverse events reports using the global safety database
· Literature review for current products
· Authoring of standard operating procedures and contributing to the Pharmacovigilance processes
· Creation of safety reports for regulatory dossiers ensuring quality control at all times.
In order to be considered for this role you must be able to demonstrate the following:
· Life-science degree with a strong understanding of medical terminology
· Excellent attention to detail, be well-organised and able to deal with conflicting priorities
· Keen to broaden your knowledge in drug safety

Due to the nature of the role, you will also be required to demonstrate excellent communication skills both oral and written including narrative writing.

This is a fantastic opportunity for someone looking to make their first move into Pharmacovigilence following previous experience in pharmaceuticals. Alternatively, exceptional recent graduates will also be considered.

For a confidential discussion about this role contact Emma on 01279 657716 or emma@seltekconsultant.co.uk

Job Ref: 8738



More Info/Apply

Regulatory Affairs (Contract) - UK

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

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

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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

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

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