Clinical Trial Data Manager
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Detailed job description and main responsibilities
For further details with regard to this vacancy opportunity, please see the attached Job Description and Person Specification.
We reserve the right to close the advert early in the event of high levels of interest. Therefore early applications are encouraged.
Please note that, in line with UKVI regulations, this vacancy does not meet the eligibility criteria for sponsorship under the Skilled Worker Visa route. As a result, we are unable to issue a Certificate of Sponsorship for this position.
We remain committed to fair and equal recruitment practices and encourage applications from all suitably qualified candidates who have the right to work in the UK.
Person specification
Application Completion
Essential criteria
- ALL sections of application form FULLY completed
Education/ Qualifications
Essential criteria
- Educated to diploma level or equivalent standard in subjects relevant to role
- Ability or willingness to undertake additional training to degree level or equivalent knowledge & experience in Respiratory research environmen
Desirable criteria
- Degree level education in related field
Knowledge, Training & Experience
Essential criteria
- Considerable Administrative experience in clinical trials environment
- Base level of theoretical knowledge of ICH-GCP clinical trial standards and the detailed trial-specific rules it provides for administration and record keeping - if formal training not already undertaken, willingness to undertake training course to acquire this knowledge within 3 months of starting in post
- Ability to prioritise own work load and delegate tasks as appropriate
- Appreciation of need for confidentiality at all times
- Producing material by utilising all areas of Windows software
- Experience of research databases, inputting patient data and answering queries
Desirable criteria
- Experience of multi agency working
- Knowledge of Respiratory Medicine
- Knowledge of Data Protection act and training
Communication and Interpersonal Skills
Essential criteria
- Clear and concise documentation in hospital/medical notes
- Ability to collect and distribute trial data and study documentation, which is often of considerable volume
Desirable criteria
- Good Presentation and teaching skills along with excellent keyboard skills
Special Attributes and other
Essential criteria
- Ability to remain calm and professional and cope with occasional exposure to distressing or emotional circumstances or work under pressure.
- Caring, friendly disposition
- Patient and understanding
- Able to work in a busy clinical environment as part of a multi-disciplinary team.
- Interested in personal development
Desirable criteria
- Ability to work without supervision in some areas: e.g telephone enquires and manage own case load
Other Requirements
Essential criteria
- Ability to carry out research and development as a requirement of the job;
- Ability to facilitate a high quality research service
- Ability to meet the needs of staff, patients and carers involved in the research and development activity of the service.
- Ability to collect and collate trials data and complete trial documentation, maintaining all Study Site Files to ICH-GCP standards and in a condition that would pass inspection by the medicines and healthcare Products regulatory Agency:
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