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Searched in jobs for keywords clinical and research
Results are ordered by date. Older jobs are included as that agency may have other jobs that fit the search: clinical research.
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- QC CHEMIST
- posted on 03/08/2004
location Bedfordshire United Kingdom, Hampshire
description Our client (part of Fisher Scientific International Inc.) is one of the world’s leading manufacturers of microbiological culture media and other diagnostic products used in clinical, food and pharmaceutical laboratories. Employing 800 staff in 14 countries, with around 370 people based in Basingstoke. A highly profitable and cash-generative business, our client boasts world-class production techniques, with ongoing investment into SAP, and accreditations such as BS5750, ISO9001 and EN46001 for medical devices. They wish to recruit an analytical chemist to fill a laboratory position within their Company. Reporting to the Chemistry Manager, the successful applicant will have responsibility for a range of QC activities within the Company including metals by AA, wet chemistry methods such as total nitrogen and chlorides and HPLC. The appointed candidate may also contribute to the development of new analytical methods. Key elements of this position are: • Follow standard methods for the analysis of products and raw materials, using a range of wet methods • Contribute to the development of new methods. • Work effectively in a team and provide an efficient analytical service. The successful candidate will be a recent graduate with a good honours degree (or HND) in Chemistry or related topic. Salary on appointment will be in the region of £16,000-£17,000 per annum. Other benefits include a contributory defined benefits (final salary) pension scheme, life assurance and private medical insurance. The closing date is 27th August 2004 If you are interested in this challenging position, please send your CV via the button shown.
skills QC CHEMIST
- Research Nurse
- posted on 29/07/2004
location Greater London West London
description The research nurses are responsible to the Deputy Clinical Operations Manager, and the Medical Director, for the conduct of phase 1 clinical pharmacology studies in healthy volunteers which are carried out in the research unit. Will be responsibvle for helping in the setting up of the research clinics, carring of patients, monitoring of progress and reporting and problems, assisting with the write up of such research etc. Full JD available.
skills Must be a UK registered nurse and have experience of Phase 1 Research
- Clinical Research Associate (Phase 1)
- posted on 29/07/2004
location Greater London West London
description No fixed hours for this post although during days in the office the Clinical Research Associate is expected to be present between 9 and 5. This will include some weekends and evenings though. Must have good knowledge of CCRU SOP's and ICH GCP Guidelines. Will need to maintain an effective tracking system for the status of each Phase 1 CRF and ensure that the CRFs have been correctly completed. A Full Job description is available upon request and submission of interest in this job.
skills Must have a good knolwedge of CCRU SOP's and ICH GCP guidelines. Also good knowledge of drug and PK samples management in CCRU.
- Senior Statistican
- posted on 17/02/2004
location UK San Francisco
description Our client is a company with a quarter-century track record of delivering on the promise of biotechnology. Today, it is among the worlds leading biotech companies, with 12 protein-based products on the market for serious or life-threatening medical conditions and 20 projects in the pipeline. With its strength in all areas of the drug development process - from research and development to manufacturing and commercialization – they continue to transform the possibilities of biotechnology into improved realities for patients. This client has been voted one of the best employers to work for Year after year due to there outstanding benefits package and fantastic work environment.
They are currently seeking to expand their oncology statistical teams with a Senior Biostatistician.
Working on RITUXAN As the lead of a clinical assessment team, collaborates in the preparation and review of clinical assessments. Provide statistically sound experimental design and data analysis input to meet project objectives and FDA statistical requirements. Working directly on submissions, one mid this year, one early next and following. Review all project protocols, author protocol statistical analysis sections and generate study randomizations. Develop study analysis plans. Reviews case report forms to ensure that protocol objectives are met and project standards are maintained. Develops statistical programs as necessary to perform analyses, prepare data displays, and verify data accuracy and validity. Author’s statistical analysis results in the clinical study report. Responsible for seeing the report through the review process. Supplies statistical input for BLA submissions and in response to FDA questions. Provides support for investigator publications. Keeps abreast of new developments in statistics, drug development, and regulatory guidance through literature review, workshop attendance, etc.
skills In order to be considered you should have:
• Experience with statistical software packages such as SAS and S-Plus.
• Sound knowledge of theoretical and applied statistics.
• Sound understanding of regulatory guidelines in a pharmaceutical research setting.
• Effective communication skills.
• Effective team contributor.
Senior Biostatistician role you should have 4-6 years clinical trail experience with a PhD.
- Drug Safety Specialist
- posted on 13/11/2003
location England Midlands, Leicester
description Providing Drug Safety support to clinical studies, within our large pharmaceutical client within the areas of respiratory and inflammation and cardiovascular therapy. Main activities within the role will include protocol, CRF review, investigator and monitor training, AE coding, SAE (serious adverse events) reconciliation and clinical study report review.
skills Ideally you will possess 1-2 years Drug Safety or Clinical Research experience, both within post marketing and clinical development. Hold excellent communication skills and have a thorough attention to detail to review and interpret clinical data.
- Regulatory Affairs Project Manager
- posted on 29/09/2003
location Wiltshire
description Our client is an AIM listed pharmaceutical group developing a portfolio of prescription medicines derived from cannabis to meet patient needs in a wide range of therapeutic indications. Working closely with officials from the Home Office, they maintain control over all aspects of the product development process - botanical research, cultivation, extraction, formulation into drug delivery technologies, clinical trials and regulatory affairs. They are now looking to recruit a Regulatory Affairs Project Manager to join the team at their Wiltshire office where the number of projects and countries covered is rapidly expanding. The successful candidate will possess a life science degree, have 3-4 years experience in Regulatory Affairs, have good verbal and written communication skills and enjoy working both in a team and independently. Ideally, the candidate will also have particular experience in clinical issues and in the Mutual Recognition Procedure. All aspects of Regulatory Affairs through from Clinical Trials Applications, preparation of all Modules of the Common Technical Document, submission of variations and an International dimension will be in store. Skill in interacting with colleagues throughout the company on different sites, and co-ordinating timely submissions to the Authorities will be required.
skills Experience, BSc
- Product Manager
- posted on 07/08/2003
location Cambridgeshire
description Product Manager, Flow Cytometry. Our client is a world leader in advanced cellular analysis of cancer and other human diseases. They manufacture a wide range of innovative instrumentation, reagents and diagnostic products. These are used by healthcare institutions, life science researchers, hospitals and industry worldwide. This role would suit a high calibre marketing professional to champion their range of Flow Cytometry instruments and reagents in the UK, to life science, research and clinical diagnostic markets. The successful candidate will be required to: · Actively manage the product portfolio through innovative commercial strategies and targeted promotional campaigns to achieve revenue goals. · Design and implement the short and medium term marketing and sales plans for the business area and provide input into corporate and strategic business plans. · Organise and provide pricing strategies and launch activities for new products. · Maintain and develop a wide range of contacts with opinion leaders in flow cytometry. Provide training to sales force, customers and staff on new products Our client is ideally seeking someone with a science degree and a formal marketing qualification. A strong background in Flow Cytometry with hands-on laboratory experience is required. Also necessary for this role is a thorough understanding of the sales process gained by a minimum of 2 years experience as a senior sales professional, product specialist, technical applications or support role.
skills BSc, MBA, Msc. Marketing.
- Data Manager
- posted on 18/07/2003
location Greater London
description Data Manager:- £25500 p/a
My client are the leading researcher in the battle against cancer in the UK.
They were established in 1909 to investigate the causes of cancer and develop new strategies for its prevention, diagnosis, treatment and cure.
The centre is the first centre in the UK entirely devoted to breast cancer research. Our goal is to advance research into the causes, diagnosis and treatment of breast cancer. We are located in new laboratory space with excellent core facilities and funding.
We are looking to recruit an experienced data manager to provide a data management service to the Breast Cancer Pathology group and Breakthrough Centre.
Responsibilities:
The Data manager will be working closely with other members of the team. The duties will include Data entry, managing the various databases derived from clinical, pathological and molecular investigations carried out by the group in a confidential manner and keeping the datasets backed up. The data manager will also liaise with other colleagues within the centre to coordinate sample collections from a local hospital.
If appropriate, the person will also work closely with the bioinformatics group within the centre.
Experience and skills:
•Excellent IT skills
•SQL server 2000
•Oracle 9i
•Microsoft Access (Essential)
•Querying / Analysis of data (Essential)
•Design of simple forms in Access (Essential)
•Medical / scientific background
•Data Input
•Data Analysis
You must be highly organised and have the ability to co-ordinate with various groups of people.
If you have all the necessary experience then we want to hear from you now. Please send your CV to stewart@pacificnorth.co.uk
Only those applicants that have all necessay experience and are put forward can be contacted due to the high level of interest. Thank you for your co-operation.
skills Medical / scientific background advantage
Access 2000
Excellent IT skill
Data input analysis
SQL server 2000
Oracle 9i
- Clinical Research Associate
- posted on 30/06/2003
location Berkshire
description To join this highly successful organisation you should have 1-2 years experience in selecting investigators, site initiation, monitoring on and off-site and have experience with study close down. You will be involved in recruitment of investigators, reviewing study documentation, compliance with regulatory requirements, attending meeting, raising queries and performing source document verification.
skills Clinical Research, Monitoring, Recruitment, Regulatory Submissions.
- Clinical Research Associate
- posted on 30/06/2003
location Berkshire
description To join this highly successful organisation you should have 1-2 years experience in selecting investigators, site initiation, monitoring on and off-site and have experience with study close down. You will be involved in recruitment of investigators, reviewing study documentation, compliance with regulatory requirements, attending meeting, raising queries and performing source document verification.
skills Clinical Research, Monitoring, Recruitment, Regulatory Submissions.
- Clinical Research Associate
- posted on 30/06/2003
location Berkshire
description To join this highly successful organisation you should have 1-2 years experience in selecting investigators, site initiation, monitoring on and off-site and have experience with study close down. You will be involved in recruitment of investigators, reviewing study documentation, compliance with regulatory requirements, attending meeting, raising queries and performing source document verification.
skills Clinical Research, Monitoring, Recruitment, Regulatory Submissions.
- Clinical Research Associate
- posted on 30/06/2003
location UK Home Counties
description You will be involved in assisting in internal/external clinical studies and includes protocol and CRF development, submission of regulatory documentation, co-ordination of study documentation. This is an interesting and varied role and includes training of site personnel along with responsibility for providing support for both national and international clinical investigations.
skills Clinical Research, Clinical Reporting/Documentation, Training.
- Clinical Research Associate
- posted on 30/06/2003
location UK Paris
description Successful and expanding CRO/Medical Devices company require Clinical Research Associate with experience to monitor projects throughout France, quality assurance and compliance with study protocol and procedures, SOPs and GCP and other regulatory requirements. Life sciences degree essential and with minimum 1 years experience. Willingness to learn and travel, and excellent English and French language skill essential.
skills Clinical Research, Clinical Trials, Monitoring, SOPs and GCP, Phase I-III
- Clinical Research Associate
- posted on 30/06/2003
location England South East
description Highly successful multinational pharmaceutical company based in the South East require a Clinical Research Associate to work on Phase I to IV clinical studies. You will assist in the monitoring of trial sites across the UK to ensure quality, compliance with study protocol, procedures, SOPs and with GCP and other regulatory requirements.
skills Clinical Research, monitoring, study protocol, procedures, SOPs, GCP.
- GCP AUDIT / AUDITOR OR GOOD CLINICAL PRACTICE CRA
- posted on 07/05/2003
location England NORTHAMPTON OR NORTHAMPTONSHIRE
description GCP OR CRA WITH LIFE SCIENCES BACKGROUND ? IDEALLY YOU WILL HAVE OVER 2 YEAR COMMERCIAL EXPERIENCE AS A CRA - CLINICAL RESEARCH ASSISTANT OR AUDITING/ QA WITH SOUND KNOWLEDGE OF THE GOOD CLINICAL PRACTICE DIRECTIVE. EXCELLENT OPPORTUNITY WITHIN A MAJOR COMPANY ... PHARMACEUTICAL OR BIOSCIENCES INDUSTRY EXPERIENCE EXTREMELY ADVANTAGEOUS. MUST HAVE A DEGREE IN LIFE SCIENCES. E-MAIL YOUR CV NOW TO: CVS@LEOSIT.CO.UK OR CALL ON 0845 009 2250
skills AUDIT AND GCP DIRECTIVE OR CRA - CLINICAL RESEARCH ASSISTANT , LIFE SCIENCES
- GCP AUDIT / AUDITOR OR GOOD CLINICAL PRACTICE CRA
- posted on 07/05/2003
location England EAST ANGLIA OR CAMBRIDGE OR NORFOLK OR SUFFOLK
description GCP OR CRA WITH LIFE SCIENCES BACKGROUND ? IDEALLY YOU WILL HAVE OVER 2 YEAR COMMERCIAL EXPERIENCE AS A CRA - CLINICAL RESEARCH ASSISTANT OR AUDITING/ QA WITH SOUND KNOWLEDGE OF THE GOOD CLINICAL PRACTICE DIRECTIVE. EXCELLENT OPPORTUNITY WITHIN A MAJOR COMPANY ... PHARMACEUTICAL OR BIOSCIENCES INDUSTRY EXPERIENCE EXTREMELY ADVANTAGEOUS. MUST HAVE A DEGREE IN LIFE SCIENCES. E-MAIL YOUR CV NOW TO: CVS@LEOSIT.CO.UK OR CALL ON 0845 009 2250
skills GCP DIRECTIVE OR CRA - CLINICAL RESEARCH ASSISTANT , LIFE SCIENCES
- Research Nurse / Study Site Coordinator / CRA
- posted on 10/04/2003
location Scotland Glasgow
description Our client requires an experienced Research Nurse / Study site Coordinator. The Candidate must have 1 - 2 Pharmaceutical experience. as well as source data verification, ICH / GCP standard compliance, proven clinical research, operational knowledge of clinical trials, phase iii - full development knowledge required.
skills clinical research
CAR
ICH / GCP
Clinical trials
- GCP AUDIT / AUDITOR OR GOOD CLINICAL PRACTICE CRA
- posted on 01/04/2003
location England NORTHAMPTON OR NORTHAMPTONSHIRE
description GCP OR CRA WITH LIFE SCIENCES BACKGROUND ? IDEALLY YOU WILL HAVE OVER 2 YEAR COMMERCIAL EXPERIENCE AS A CRA - CLINICAL RESEARCH ASSISTANT OR AUDITING/ QA WITH SOUND KNOWLEDGE OF THE GOOD CLINICAL PRACTICE DIRECTIVE. EXCELLENT OPPORTUNITY WITHIN A MAJOR COMPANY ... PHARMACEUTICAL OR BIOSCIENCES INDUSTRY EXPERIENCE EXTREMELY ADVANTAGEOUS. MUST HAVE A DEGREE IN LIFE SCIENCES. E-MAIL YOUR CV NOW TO: CVS@LEOSIT.CO.UK OR CALL ON 0845 009 2250
skills AUDIT AND GCP DIRECTIVE OR CRA - CLINICAL RESEARCH ASSISTANT , LIFE SCIENCES
- GCP AUDIT / AUDITOR OR GOOD CLINICAL PRACTICE CRA
- posted on 01/04/2003
location England EAST ANGLIA OR CAMBRIDGE OR NORFOLK OR SUFFOLK
description GCP OR CRA WITH LIFE SCIENCES BACKGROUND ? IDEALLY YOU WILL HAVE OVER 2 YEAR COMMERCIAL EXPERIENCE AS A CRA - CLINICAL RESEARCH ASSISTANT OR AUDITING/ QA WITH SOUND KNOWLEDGE OF THE GOOD CLINICAL PRACTICE DIRECTIVE. EXCELLENT OPPORTUNITY WITHIN A MAJOR COMPANY ... PHARMACEUTICAL OR BIOSCIENCES INDUSTRY EXPERIENCE EXTREMELY ADVANTAGEOUS. MUST HAVE A DEGREE IN LIFE SCIENCES. E-MAIL YOUR CV NOW TO: CVS@LEOSIT.CO.UK OR CALL ON 0845 009 2250
skills GCP DIRECTIVE OR CRA - CLINICAL RESEARCH ASSISTANT , LIFE SCIENCES
- Clinical Research Associate II
- posted on 23/01/2003
location Greater London
description We currently have a permanent position for a Clinical Research Associate, based in Middlesex or Surrey depending on the candidate’s preference. You will be responsible for co-ordinating required study activities for an international CRO as required by the client. You should have a good working knowledge of, and be able to assure compliance with the ICH and FDA Good Clinical Practices, applicable regulatory and legal requirements, and company (or client, according to exhibit) Standard Operating Procedures. You should have a degree or equivalent in life sciences, and have at least one years experience as a CRA. This position will involve travel around 3 days per week, and as such you should be flexible, and be open to overnight stays.
skills Life Sciences Degree or equivlent
Knowledge of GCP/ICH-FDA guidleines
1 years CRA experience
- SAS (Clinical) Programmer
- posted on 20/06/2002
location Bedfordshire
description My client is looking for a SAS Programmer to join the small Biostatistics team and take a full part in the international project teams. You will be responsible for programming and producing the statistical tabulations and analysis warehouses for clinical trial reports. As well as writing study specific software you will have the opportunity to develop generic programs with a view to improving the efficiency and quality of the work of the team. You should have good SAS programming skills and be able to work both in a team environment and independently. Previous work experience within the Pharmaceutical or contract research industry would be advantageous.
skills Clincal SAS Programmers
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