Brand New Role: Clinical Trials Associate Location: Edinburgh (office-based, with some UK travel) My client, a specialist cancer Research & Charity organisation, is experiencing strong growth as their network of Clinical trials continues to expand across the UK. As a result, they are now seeking a dynamic & outgoing Clinical Trials Associate to work alongside the UK Programme Manager in their Edinburgh office. This is ...
Our client, an expanding pharmaceutical company is seeking a Clinical Research Associate (CRA) to join its team on a 12 month contract. The Clinical Research Associate will report to the Director of Clinical and your key responsibilities will include: • Providing support to the Clinical Study Team for the planning and execution of clinical trials. • Assist with the development and revision of ICF, pharmacy manuals, samp...
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Date: 19 April
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Guildford, Surrey
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£23,000 - £26,000 per annum, negotiable
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39 applications
Clinical Research Associate We are seeking an experienced CRA or a Coordinator who would like to progress to a CRA after training etc, . Urgently seeking a CRA to work near Guildford, Surrey on a permanent basis. Our Client is a Clinical Research Organisation (CRO) specialising in medical device clinical research. As a company that undertakes in-house clinical research as well as multi-site cl...
The responsibility of a Clinical Monitoring Associate (CMA) is to perform remote clinical monitoring tasks and remote visits for designated projects in accordance with relevant SOPs, study specific procedures and regulations. Responsibilities include managing/supporting clinical monitoring activities remotely, including but not limited to issue resolution, patient enrollment management, handling protocol and/or contract amendments, and e...
A provider of unparalleled scientific and regulatory leadership to pharmaceutical, biotechnology, contract research organisations (CROs) and medical device companies whose solutions flawlessly expedite their client’s clinical research studies are currently looking for a tenacious and committed Business Development Associate. Based in Peterborough, Cambridgeshire, you will support the sales department in the sales and marketing of bu...
Essential Function The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOPs. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required), performing q...
Job Description: We are assisting our client in recruiting a Senior Clinical Research Associate. This is a permanent position office based in Cambridgeshire. Under limited supervision, the Senior CRA monitors and oversees clinical practices for one or more multi-site clinical trials, ensuring compliance with all regulatory agency requirements. Maintains sound clinical practices to ensure validity of study. Monitors the cond...
PAREXEL International is a growing, fast-paced, global Clinical Research Organization (CRO) that has helped bring to market 49 of the top 50 selling pharmaceuticals. In fact, we have worked with all 10 of the world's top 10 pharmaceutical companies. Given our breadth of expertise and the trust placed in us by major pharmaceutical companies worldwide, PAREXEL can provide you with a number of career options in Clinical Researc...
The Company My client is a Global Biopharmaceutical company with a robust pipeline of products who is as committed to its future growth as it is to its staff, they want to be able to offer a good work life balance and as such offer a competitive, flexible benefits package. The Role Due to continued growth they are now looking to appoint an Associate Director of Pricing & Market Access with responsibility for ...
Position: Analyst - Oncology and Hematology Salary: Competitive, depending on experience. GlobalData is an international company with key offices in London, United States, and Asia. We are a Business Intelligence provider, supporting many top companies in the pharmaceutical and medical equipment space. We provide market, competitor, product, and customer information along with in-depth research, analysis, ...
Job Description: Our client is seeking a Regulatory Affairs Associate II based in Berkshire Duties will include: Supports regulatory affairs and technical writing activities. Compiles and submits clinical trial applications and notifications to regulatory authorities and ethics committees. Ensures clinical trials are conducted such that subject's rights, safety and well being are protected and that the clinica...
Job Description: Our client is seeking a Senior Regulatory Affairs Associate based in Berkshire. - Compiles and submits clinical trial applications and notifications to regulatory authorities and ethics committees. - Ensures clinical trials are conducted such that subjects’ rights, safety and well being are protected and that the clinical trial data are reliable. - Provides regulatory affairs advice and support...
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Date: 2 May
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Germany,
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Competitive salary
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1 application
Job Description: Our client is a growing CRO looking for a Senior CRA to be based in Germany, either office based (Cologne) or home-Based (within easy reach of Berlin, Munich or Frankfurt). Job Summary: - Administration and full investigator site responsibility for clinical studies according to our clients Standard Operating Procedures (SOPs), ICH-GCP and local ...
5 jobs matching this search were posted in the last week
Springer Healthcare is a full service agency and leading publisher of medical educational products for the healthcare community, and forms part of Springer Science+Business Media, one of the world’s leading global scientific and medical publishers. We are recruiting for an Associate Medical Writer to join our London based team to prepare scientific content of medical communications that satisfy client needs in terms of quality, c...
Job Description: With the growth of their market access and healthcare value demonstration activities our client, a leading Market Access, Health Economics and Outcomes research consultancy, wishes to appoint an ambitious (senior) Research Associate with a genuine passion for understanding and communicating the science of healthcare value. The role will involve contributing to international projects by performing both quali...
Job Description: Our client, a leading Market Access, Health Economics and Outcomes research consultancy, is looking to recruit a highly motivated Research Associate in their Endpoint Development & Outcomes Assessment team, who is looking to apply and enhance their healthcare research skills in a challenging and rapid-moving field. This is an exciting and varied role in which you will be involved in studies focused on ...
Job Description: Our client, a leading Market Access, Health Economics and Outcomes research consultancy, is looking to recruit a highly motivated Market Access Director or Associate Director to their Value Insight & Communication practice. This is an exciting leadership role in which you will provide scientific and strategic input to various types of market access projects. Whilst supporting the growth and development ...
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Date: 9 May
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Germany,
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Competitive salary
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9 applications
Location: Germany - Berlin PAREXEL International is a growing, fast-paced, global Clinical Research Organization (CRO) that has helped bring to market 49 of the top 50 selling pharmaceuticals. In fact, we have worked with all 10 of the world's top 10 pharmaceutical companies. Given our breadth of expertise and the trust placed in us by major pharmaceutical companies worldwide, PAREXEL can provide you with a number of career options i...
We are looking for a CRA for our client who can either be office based in Hertfordshire or Field based in the Midlands or in Southern England. Responsible for monitoring our client’s clinical trials to ensure that investigators are conducting the research within requirements of the clinical protocol, that research is conducted in accordance with applicable federal regulations / EU Directive and guidelines, that data quality on in...
Contract CRA/SCRA Category: Pharma Type: Contract Location: South West- UK Daily Rate: £200-£270 Are you a competent clinical research associate looking for a new contract position? If so I’m working with a client that you need to know about. My client is one of the most reputable pharma companies in the world and has been recognised as being one of the best places to work globally....
Company Profile NWeH develop innovative software for healthcare research within the NHS, public and private sector. We are a not-for-profit collaborative venture between Salford Royal Foundation Trust (SRFT), Salford Teaching Primary Care Trust (Salford PCT) and the University of Manchester, an arrangement which gives us unique access to health expertise and data. We were established in 2008 and over the pas...
Regulatory Affairs Associate, Chemical. Shardlow, UK. Salary based on experience. Leading global provider of essential non-clinical contract research and services to the chemical, agrochemical, pharmaceutical, biotech and medical device industries is seeking for a Regulatory Affairs Associate to join their Department of Registration Services based in their laboratories in Shardlow, England. Responsibilities include provi...
Perceptive Informatics, Inc., a subsidiary of PAREXEL, provides advanced technology solutions, including medical imaging, to facilitate the clinical development process. PAREXEL International is a growing, fast-paced, global Clinical Research Organization (CRO) that has helped bring to market 49 of the top 50 selling pharmaceuticals. In fact, we have worked with all 10 of the world's top 10 pharmaceutical companies. I...
QLAB, based in Livingston, is a central laboratory where clinical trial samples collected from patients are sent for analysis. Our world-class laboratory provides full analytical support for a huge variety of analytical techniques. Our team of Project Service staff organize, set up and run these clinical trials both regionally and globally. They are involved in all aspects of trials working alongside Finance, Contracts, Regulatory Affairs,...
Job Description: Our client is a globally recognised top CRO who are looking for a Senior Clinical Monitoring Associate to be based in West London. The responsibility of a Senior Clinical Monitoring Associate is to independently perform and organize remote clinical monitoring tasks and visits for designated projects in accordance with relevant SOPs and regulations. Responsible for coordinating a moderate to large ...
