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Covance
Clinical Research Associate
Clinical Research Associate 2
UK
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Clinical Professionals
Biochemistry
Senior Clinical Research Associate SCRA in Czech Republic (home based)
Rest of Europe
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| Company: |
Covance |
| Category: |
Clinical Research Associate |
| Position: |
Clinical Research Associate 2 |
| Area: |
West Midlands |
| Location: |
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| Notes: |
YOUR CAREER - IS NOT JUST A PHASE, IT’S A WAY FOR LIFE.
Covance manages over 15,000 clinical trial protocols in 100 countries and 6 continents. To sustain our growth, we continue to invest significantly in new facilities around the globe. Covance has never been more financially and operationally strong and with current positive industry trends, we are poised for continued success.
Help bring new miracles of medicine to market sooner. Join the Clinical Research team at Covance. You’ll be working with respected medical professionals, helping them win the war against disease. As a key member of one of the world’s largest, most comprehensive drug development services companies, you’ll receive the finest training and greatest advancement opportunities. So make the career decision of your life. Advance with Covance.
CoSource, our insourcing division provides you with the opportunity to work directly for our clients. For these roles you will either work out of our client offices or field based – and see clinical trials from the clients’ perspective. We work in partnership with global and smaller pharmaceutical companies and can support you in your career development.
With clinical trial professionals located in more than a dozen countries, Covance can conduct clinical trials anywhere in the world. Covance maintains centres of excellence in study design and clinical development in oncology, CNS, infectious diseases and cardiovascular. Our innovative scientists, clinicians, regulators and health economics experts are committed to the highest quality standards. Our experience in the field offers our CRAs unsurpassed ability to learn in a wide variety of therapeutic areas!
The main activities would include:
• Provide project manager with regular study status updates
• Act as a liaison with team members internationally, including other HQ sites, as well as external service providers, as appropriate.
• Support and act as a liaison with international contract research organization (CRO) monitors and other affiliate personnel to ensure consistent conduct of study across countries.
Study Start-up:
• Participate in the review of the Protocol and Study Procedures and Manual. Provide input regarding global issues and practices related to data collection requirements for case report forms (CRFs) and other study related documentation.
• Review draft CRFs and assist in finalization and subsequent annotation for training purposes.
• Assist in the defining of essential documents for the study, manage the flow of these documents to the appropriate archives, maintain central files, and regularly interact with archive staff.
• Participate in the evaluation and assessment of potential study sites with the monitors or CRO and the project manager based on defined site selection criteria.
• Manage study drug ordering, packaging and shipping processes and coordinate review and finalization of drug labels.
• Study Implementation and Conduct:
• Coordinate and manage ordering and distribution of study supplies to monitors and sites, including CRFs and drug supplies.
• Manage tracking systems related to drug supply and use, enrolment of subjects, regulatory document flow, study timelines, financial information, study performance metrics, data flow, laboratory samples, etc.
• May manage and track Serious Adverse Events (SAEs).
• Ensure consistency in study implementation and monitoring activities by participating in site visits as appropriate, and reviewing and approving monitoring visit reports, as required.
Study Close-Down:
• Assist project manager in managing the completion of activities related to the closure of the database.
• Review essential documents stored in archives as required to assure archives are complete.
• Assist in review of drug disposition and destruction authorizations.
• Provide operational input into Final Study Report as required. |
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| Reference: |
7136BR
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| Contact: |
covance |
| Phone: |
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| Apply: |
Click Here
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