CONTRACT: SAS Programmer - Program & Report Non-Safety Data
Background:
This position would ideally suit a candidate with 2-3 years experience in SAS programming, covering dataset manipulation, Macro language, Base and Statistics procedures. The candidate will have some experience of reporting clinical trials. Accountabilities Responsibilities: Work as part of a team in the following ... more
Type: Contract Location: N/A Country: United Kingdom Posted: 11/1/2008 1:34:00 AM
|
Senior Project Manager, Early Phase: Deputise for the Director of Project Management! London
Background:
Top Senior Clinical Project Manager role in London with a highly reputable company that really believes in developing it's employees! This is a 12 month fixed term contract opportunity with a genuine possibility of going permanent afterwards.
Primary Duties:
The role ... more
Type: Full Time/Contract Location: N/A Country: London Posted: 11/1/2008 1:34:00 AM
|
Trial Data Associate
Background:
My client is a pharmaceutical company based close to London who are currently in the process of expanding there Data Management team. This expansion has resulted in my client requiring a Trial Data Associate to join the team on a permanent basis.
... more
Type: Full Time Location: Berkshire, London, Home Counties Country: Home Counties Posted: 11/1/2008 1:33:59 AM
|
CONTRACT: Senior SAS Statistical Programmer - ISE ISS
Background:
CONTRACT: Senior Statistical Programmer Phase II - IV Safety & Efficacy Programming 6 month renewable contract based in Germany Job Summary: Responsible for the input into specifications for analysis including derived datasets, listings, tables, graphs of clinical trials across Phase II-IV and ... more
Type: Contract Location: N/A Country: London Posted: 11/1/2008 1:33:59 AM
|
Regulatory Affairs Officer, Lisbon Portugal
Background:
A World's leading Pharmaceutical Services Company is looking for a Regulatory Affairs Officer to assist senior regulatory staff in the preparation or review of submissions regarding preclinical or clinical studies. This position is based in Lisbon, Portugal. Responsibilities: *Prepares and or reviews regulatory ... more
Type: Full Time Location: N/A Country: United Kingdom Posted: 11/1/2008 1:33:59 AM
|
CONTRACT: SAS Programmer II
Background:
CONTRACT: SAS Programmer II 6 month++ based in South UK Job Summary: To plan, develop and execute statistical programs designed to analyse clinical trial data. To assist experienced staff in planning, development, validation of project level programs and macros. Accountabilities Responsibilities: ... more
Type: Contract Location: Surrey Country: Home Counties Posted: 11/1/2008 1:33:59 AM
|
International Project Manager for CRO in Madrid
Background:
A leading global bio pharmaceutical services organization is currently looking for a Clinical Lead for its office in Madrid Spain to manage clinical monitoring activities and liaise with project management and the sponsor if appropriate to ensure that the clinical deliverables are ... more
Type: Full Time Location: N/A Country: United Kingdom Posted: 11/1/2008 1:33:58 AM
|
Senior Clinical Research Associate - CRA
Background:
Paramount Clinical Research: Senior Clinical Research Associate CRA An international Clinical Research Organisation is currently looking for a Senior Clinical Research Associate CRA to join the team, ideally based in their Berkshire office. The primary function of a Senior Clinical Research ... more
Type: Full Time Location: Berkshire Country: Home Counties Posted: 11/1/2008 1:33:58 AM
|
CRA with cardiovascular experience
Background:
Main Duties & Responsibilities: *Reporting directly to the Project Manager *On-site monitoring *Regulatory and ethics submissions *In-house monitoring *Study tracking *Support of the Trial Leaders and Project Managers *maximum of 3 visits per week as per contract Requirements: *Life science degree ... more
Type: Full Time Location: N/A Country: Italy Posted: 11/1/2008 1:33:58 AM
|
Contract CRA
Background:
My Client is a Pharmaceutical company they are looking for a Clinical Research Associate to work on a 6 month contract. You will be involved in site selection and, ethical submissions and monitoring sites. You will be reporting to the Clinical Project Manager. Previous CRA ... more
Type: Contract Location: England Country: UK Posted: 11/1/2008 1:33:58 AM
|
Experienced Data Manager - West Sussex
Background:
Paramount Recruitment: Clinical Data Manager, Pharmaceutical Company - Sussex. Are you an experienced and driven Clinical Data Manager looking to move your career to the next level in a leading Pharmaceutical company? A fantastic opportunity has arisen for an experienced Clinical Data Manager ... more
Type: Full Time Location: N/A Country: United Kingdom Posted: 11/1/2008 1:33:57 AM
|
|
EASY PROGRESSION FOR CRA
Background:
CRAs/SCRAs GLOBAL REQUIREMENTS - JOIN MY CLIENT AS THEY BUILD UPON AN ENVIABLE REPUTATION TO WORK INTO THE FUTURE, DELIVERING HIGH-CLASS RESULTS! Are you a conscientious, hard working Clinical Researcher looking to excel in your career? Do you wish to be fully ... more
Type: Full Time Location: N/A Country: Hungary, Poland, Romania, Ukraine, Italy Posted: 11/1/2008 1:33:57 AM
|
Regulatory Affairs Manager
Background:
To establish and maintain the regulatory affairs department. To comply with all regulatory and safety requirements for all marketed products and to work in conjunction with the regulatory affairs department based in Germany. To maintain compliance for products authorized via the MRP or DCP. ... more
Type: Full Time Location: Buckinghamshire Country: Home Counties Posted: 11/1/2008 1:33:57 AM
|
CRA, permanent, Milan
Background:
Clinical Research Associate CRA Rapidly growing and well-established Italian International Contract Research Organization CRO , based in Milan, and working with the top American pharmaceutical companies, is urgently looking for an experienced Clinical Research Associate to monitor very interesting international projects and work ... more
Type: Full Time Location: N/A Country: Italy Posted: 11/1/2008 1:33:57 AM
|
Senior Clinical Research Associate, Lisbon
Background:
A World's leading Pharmaceutical Services Company is looking for a Senior Clinical Research Associate SCRA to join their team in Lisbon. Responsibilities: As a Senior CRA you will oversee the progress of a Clinical Trial, ensuring that it is conducted, recorded ... more
Type: Full Time Location: N/A Country: United Kingdom Posted: 11/1/2008 1:33:56 AM
|
Freelance Biostatistician Statistician Phase I-III Trials-SAS
Background:
In this challenging position you will be responsible for playing a leading role in managing statistical activities, including timelines, resources and deliveries related to an entire clinical development project. Essential Requirements A Masters in Biostatistics Statistics or an applied field of statistics. Hands-on ... more
Type: Contract Location: N/A Country: Germany Posted: 11/1/2008 1:33:56 AM
|
CONTRACT Oracle Clinical Programmer for Major EDC Project
Background:
Essential, mimimum 3 yrs pharmaceutical CRO experience, minimum 2 yrs+ Oracle Clinical OC experience i.e. building databases database developemnt work programming Oracle clinical , clinical data management, must be a self starter. Desirable, electronic data capture experience ... more
Type: Contract Location: N/A Country: United Kingdom Posted: 11/1/2008 1:33:56 AM
|
Regulatory Affairs Officer, Lisbon Portugal
Background:
A World's leading Pharmaceutical Services Company is looking for a Regulatory Affairs Officer to assist senior regulatory staff in the preparation or review of submissions regarding preclinical or clinical studies. This position is based in Lisbon, Portugal. Responsibilities: *Prepares and or reviews regulatory ... more
Type: Full Time Location: N/A Country: United Kingdom Posted: 11/1/2008 1:33:56 AM
|
Pharmacovigilance Officer
Background:
Pharmaceutical company
Primary Duties:
• You will handle spontaneous cases within the UK • Information collection and quality control for PSUR • You will review ADR report forms for clinical trials protocol to comply with the ... more
Type: Full Time Location: Cheshire Country: North West Posted: 11/1/2008 1:33:55 AM
|
Clinical Research Associate
Background:
My client is one of the most established Global pharmaceutical companies in the market. They now seek a CRA to join their team to operate on an initial 12month contract. Adhering to the current international guidelines you will be monitoring sites across Sweden working on ... more
Type: Contract Location: N/A Country: Sweden Posted: 11/1/2008 1:33:55 AM
|