Clinical Research Jobs in Hertfordshire
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UK- Clinical Research Associate- Oncology
- Salary:
- On application
- Location:
- Stevenage, Hertfordshire, England
- Job Type:
- Permanent
- Date Posted:
- 25-May-2012 00:00Add to My Shortlist
Novella Clinical is a global full service eCRO, committed to providing an outstanding service to our client's as well as our employees. We focus on providing excellent training and career development opportunities, encouraging growth from within our talented work force. Our parent company is one of the World's leading not profit research organisations, and you will be joining a passionate... including drugs, CRFs, diary cards, consent forms Organise and track investigator payments Provide study updates to regulatory bodies To be considered for this position you will be required to have a science degree or equivalent, be able to display a clear understanding of the drug development process, be familiar with clinical research terminology and have related UK experience such as previous monitoring experience, study site coordinator, Research Nurse. This position will offer excellent training and development for the successful candidate. Oncology experience is essential Novella Clinical is committed to providing an outstanding service to client's as well as employees. Focusing on excellent...
UK- Experienced Senior Clinical Research Associate
- Salary:
- Competitive
- Location:
- Cambridgeshire, Huntingdonshire, Bedfordshire, Hertfordshire, Northamptonshire, Norfolk
- Job Type:
- Permanent
- Date Posted:
- 29-May-2012 00:00Add to My Shortlist
An interesting and varied Lead/Senior Clinical Research Associate vacancy has arisen with our client; a progressive Clinical Research Organisation and regulatory consultancy which specialises in providing practical advice and support to the pharmaceutical industry to move products from early concept and into the clinic. Their main area of focus is in early Phase clinical trials. The Senior CRA will be responsible for monitoring...
Clinical Research Associate - UK (Cambridgeshire)
- Salary:
- On Application
- Location:
- Cambridgeshire, Huntingdonshire, Bedfordshire, Hertfordshire, Northamptonshire, Norfolk
- Job Type:
- Permanent
- Date Posted:
- 25-May-2012 00:00Add to My Shortlist
A Clinical Research Associate vacancy has arisen at an expanding clinical and regulatory consultancy which specialises in providing practical advice and support to the pharmaceutical industry to move products from early concept and into the clinic. Their main area of focus is in early Phase I and Phase II clinical trials. This is a permanent, full-time position requiring focussed on monitoring at...
Clinical Research Executive (Cambridgeshire)
- Salary:
- On Application
- Location:
- Cambridgeshire, Huntingdonshire, Bedfordshire, Hertfordshire, Northamptonshire, Norfolk
- Job Type:
- Permanent
- Date Posted:
- 30-May-2012 00:00Add to My Shortlist
An interesting and varied Clinical Research Executive vacancy has arisen with our client, an expanding clinical and regulatory consultancy which specialises in providing practical advice and support to the pharmaceutical industry to move products from early concept and into the clinic. Their main area of focus is in early Phase I and Phase II clinical trials. The Clinical Research Executive (CRE) will...
Consultant Dermatologist Dermatology
- Salary:
- New Consultant Contract
- Location:
- Stevenage, Sg1 4ab
- Job Type:
- Contract/Temp
- Date Posted:
- 26-May-2012 00:00Add to My Shortlist
East & North Hertfordshire NHS Trust Advert East & North Hertfordshire NHS Trust Locum Consultant in Dermatology Applications are invited for a Locum Dermatology Consultant post to commence as soon as possible based at the East & North Herts NHS Trust with a view to a substantive appointment. This post represents replacement for retirement and newly available sessions. It will... applicants would be welcome. It will be predominantly based at the Lister Hospital, Stevenage but clinical duties may be undertaken on allied hospital sites. The post-holder would ideally have an interest in skin cancer and participate in the regional skin cancer network. We would encourage applicants with sub specialty and clinical research interests to apply for the positions. There will be regular CPD opportunity within the post-holder's timetable in order to attend meetings at St Johns, The Royal Society of Medicine and Watford Hospital. Applicants must be on the Specialist Register for Dermatology or be within six months of obtaining specialist registration...
Clinical Research Associate (Cra And Scra) - Award Winning Cro - Uk
- Salary:
- Competitive
- Location:
- Uk, England, South East England, Berkshire, Hampshire, London, Cambridgeshire, Hertfordshire
- Job Type:
- Permanent
- Date Posted:
- 23-May-2012 17:56Add to My Shortlist
CRA, SCRA: This global CRO is currently looking to recruit a CRA and a SCRA for their expanding UK CRA division. You will have the opportunity to work either from home or from one of their 3 UK offices on a number of therapeutic areas. This is a great role for a CRA looking to further their career with the...
Associate Director Clinical Operations Neuroscience
- Salary:
- On Application
- Location:
- Cambridgeshire, Essex, Hertfordshire, London, Middlesex
- Job Type:
- Permanent
- Date Posted:
- 24-May-2012 09:14Add to My Shortlist
JOB SUMMARY: Rare opportunity for a Senior Project Manager/Programme Manager looking to progress into an Associate Director role within a top tier Pharma Company. This role will involve both strategic and scientific leadership for assigned studies and/or have overall Clinical Operations responsibility for a specified compound within the Neuroscience portfolio. May also have responsibility for direct reports, including hiring and... History of working in complex team environments with numerous/diverse stakeholders in multiple regions. * Extensive relevant experience in the pharmaceutical industry including experience as a clinical program manager for a global study. * Line management experience preferred KEYWORDS: Senior CPM, Associate Director Clinical Development, Associate Director Clinical Operations, Neuroscience, Senior Clinical Research, Hertfordshire TO APPLY: For a confidential discussion please telephone Beccy Bray at AXESS Limited on 020 8560 2300. To apply, please send your CV to jobs@axess.co.uk quoting reference 5218 Only candidates with EU work authorisation will be considered. ABOUT AXESS: AXESS has been operating since 1990 We are a recruitment...
Top 5 Cro Requires Clinical Research Associate I (Cra I) - Uk
- Salary:
- £25k - £28k + benefits
- Location:
- Uk, England, South East England, Berkshire, Hampshire, London, Cambridgeshire, Hertfordshire
- Job Type:
- Permanent
- Date Posted:
- 30-May-2012 17:39Add to My Shortlist
CRA I - A top five international CRO is currently expanding its CRA team in the UK. As a CRA I at this award-winning organisation you will be given the opportunity to work across a broad range of therapeutic areas in Phases I to IV. Working at a large CRO such as this means plenty of exposure to more senior...
Clinical Research Associate I (CRA I) - TOP 5 CRO - UK
- Salary:
- £25k - £28k
- Location:
- England, London, Berkshire, Uk, South East England, Hampshire, Cambridgeshire, Hertfordshire
- Job Type:
- Permanent
- Date Posted:
- 23-May-2012 17:53Add to My Shortlist
CRA - An international CRO is continuing its on-going expansion of its UK CRA division. Working for this award-winning organisation will give you the opportunity to work across a broad range of therapeutic areas in Phases I to IV. This is an ideal role for a CRA looking for career progression at an internationally recognised CRO. You will have plenty...
GCP QA Auditor
- Salary:
- To Negotiate
- Location:
- England, Hertfordshire, Essex, Cambridgeshire, Bedfordshire
- Job Type:
- Permanent
- Date Posted:
- 25-May-2012 16:48Add to My Shortlist
As primarily a GCP QA Auditor within the multi-disciplined company QA team you will utilise your expert regulatory knowledge and excellent communication skills to assist with the design and implementation of the audit programme for the clinical development functions, including internal systems, external supplier and essential documentation and investigator site audits. You will also provide support, advice, education and training... Development office in Cambridgeshire, this is a highly interactive role, requiring self-reliance, effective strategic thinking and planning skills, the ability to network, operate within a busy team, and build influential relationships both internally and externally. Qualifications/experience required: * Ideally a bioscience degree or nursing qualification * Experience in GCP regulated clinical research essential * A good understanding of clinical quality assurance * Proven experience in investigator site auditing * Experience in post-marketing human medicinal product Pharmacovigilance, data management or a statistical background would be beneficial * A working knowledge of Oncology or Neuroscience would be advantageous * A full driving licence is...
Senior EU Study Manager (Oncology)
- Salary:
- On Application
- Location:
- Berkshire, Buckinghamshire, Hertfordshire, Surrey, London, Middlesex
- Job Type:
- Permanent
- Date Posted:
- 24-May-2012 09:16Add to My Shortlist
JOB SUMMARY: Senior Study Management of Phase II and Phase III Oncology studies according to ICH guidelines in support of the clinical strategies defined in the Integrated Development Plan (IDP) as they relate to European specific responsibilities. Support of Phase I trials may also be required. Office based from London HQ. BACKGROUND: Expanding Global Pharmaceutical Company EU HQ based in... the study budget; and study closeout. QUALIFICATIONS / EXPERIENCE REQUIRED: * Bachelors Degree preferably in Life Sciences, or R.N., or international equivalent. * 3+ years of clinical trial management, Study Manager / Project Manager, experience including accumulation of one year of monitoring experience required (either in a pharmaceutical company or clinical research organization). * 1+ year of European clinical trial management * Demonstrated ability to manage clinical trials * Superior communication skills: written, oral, interpersonal and presentation * Excellent problem solving and analytical skills * Must work effectively in a matrix team environment and be flexible to contribute to the needs of...
UK- Medical Device Regulatory Affairs Associate
- Salary:
- On application
- Location:
- London, Bedfordshire, Hertfordshire, Buckinghamshire, Cambridgeshire, England
- Job Type:
- Contract/Interim
- Date Posted:
- 30-May-2012 10:51Add to My Shortlist
Novella Clinical is a global, full service CRO with European Headquarters in Hertfordshire, England. We are committed to providing a superior service to our global clients, and as such we are seeking hire an experienced Regulatory Affairs Associate with a proven track record working in regulatory affairs and quality assurance in the UK or EU. The main responsibilities in this role will be to provide regulatory and quality support to select clinical research projects involving medical devices, Combination Products and Diagnostics. Working with the Director, Clinical Monitoring EU and Director of Regulatory Affairs (Global) and Regulatory Affairs Manager, EU to provide strategic regulatory guidance and information to projects; to acquire pertinent regulatory information from agencies and organizations; to support regulatory agency interactions, communications, ...
Experienced Clinical Project Manager
- Salary:
- On application
- Location:
- Cambridgeshire, Huntingdonshire, Bedfordshire, Hertfordshire, Northamptonshire, Norfolk
- Job Type:
- Permanent
- Date Posted:
- 25-May-2012 00:00Add to My Shortlist
Experienced Clinical Project Manager (Cambridgeshire, UK) An interesting and varied Clinical Project Manager vacancy has arisen with our client, an expanding Clinical Research Organisation and regulatory consultancy which specialises in providing practical advice and support to the pharmaceutical industry to move products from early concept and into the clinic. Their main area of focus is in early Phase I and Phase II clinical trials. The Project Manager will have primary responsibility for the...
Regulatory Affairs Associate
- Salary:
- On Application
- Location:
- London, Bedfordshire, Hertfordshire, Buckinghamshire, Cambridgeshire, England
- Job Type:
- Permanent
- Date Posted:
- 25-May-2012 00:00Add to My Shortlist
Novella Clinical is a global, full service CRO with European Headquarters in Hertfordshire, England. We are committed to providing a superior service to our global clients, and as such we are seeking hire an experienced Regulatory Affairs Associate with a proven track record working in regulatory affairs and quality assurance in the UK or EU. The main responsibilities in this role will be to provide regulatory and quality support to select clinical research projects involving investigational or marketed drugs, devices, biologics, or new medical procedures. Work with the Director, Clinical Monitoring EU and Director of Regulatory Affairs (Global) and Regulatory Affairs Manager, EU to provide strategic regulatory guidance and information to projects; to acquire pertinent regulatory information from agencies and organizations; to support...
Senior Manager Regulatory Affairs
- Salary:
- On Application
- Location:
- Cambridgeshire, Bedfordshire, Hertfordshire, London, Middlesex
- Job Type:
- Permanent
- Date Posted:
- 26-May-2012 00:00Add to My Shortlist
JOB SUMMARY: Exciting opportunity for an experienced regulatory specialist to join a global organisation offering excellent career progression. You will contributing to clinical development plans, global regulatory strategic plans and providing advice on EU regulatory clinical trial and marketing authorisation requirements to the International Project Teams or Regulatory Sub-team. You will also be responsible for maximising product lifecycle management and... needed. QUALIFICATIONS / EXPERIENCE REQUIRED: College or University degree required in associated functional discipline (Life Sciences, Chemistry, Toxicology or Pharmacology) Doctorate degree desired (e.g., MD, JD, Pharm D, or PhD in life sciences), advanced degree preferred (e.g., RPh) Experience required: Regulatory experience including some broader industry related experience (e.g. manufacturing, clinical research, etc.), Strong EU regulatory experience and a good understanding of US regulatory processes In depth knowledge of the EU clinical Trials Directive, Paediatric Regulation, Scientific Advice/Protocol Assistance process Extensive experience of IMPDs, submission of CTAs and the EudraCT Database Experience of the Drug Development process and working with international project...