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Vacancy details
Vacancy description:
Job Code:
WR/NOT09/23909
Job Title:
Clinical Trial Assistant
Job Category:
Clinical Research
Contract:
Permanent
Discipline:
Clinical Study Coordinator, Clinical Study Admin, Clinical Trial Administrator
Country:
United Kingdom
Location:
Hampshire
Min experience:
N/A
Annual salary:
Negotiable
Apply by:
07 Jul 2008
Clinical Trial Assistant Job - Hampshire:
Job Summary
Are you an experienced, energetic and enthusiastic Clinical Trial Assistant (CTA) looking for a challenge? Would you like to work in a modern, fast paced environment with like minded, highly dynamic, innovative and proficient individuals? Would you like the opportunity to join one of the world's leading early phase Contract Research Organisations who pride themselves on their outstanding track record and commitment to superior quality?
Our client is looking to offer the ideal candidate full support and extensive, consistent and continuous training to reach their goal. They are looking for a Clinical Trial Assistant (CTA) to join their dedicated clinical team based in Hampshire.
Job Title
Clinical Trial Assistant (CTA)
Background
As a Clinical Trial Assistant (CTA), you will assist the clinical research teams in ensuring the most effective and efficient conduct of clinical research studies by providing administration and project tracking support.
Key Responsibilities
- To support the clinical research teams with ongoing conduct of studies.
- To assist project teams with study specific documentation as appropriate; - preparing study-specific procedures - drug accountability records - completion of status reports - study newsletters and merge letters, etc.
- To become familiar with ICH GCP, appropriate regulations and relevant SOP's.
- To become familiar with the roles of the Clinical Research Associate (CRA) including site visits, if appropriate.
- To assist in the preparation, handling and tracking of Ethics/Regulatory submissions.
- To process Case Record Forms i.e. log in, tracking, quality control as appropriate for the study.
- To assist in co-ordination of Investigator payments.
- To maintain the study files for the project.
- To co-ordinate ordering/dispatch and tracking of trial materials e.g. CRFs, diary cards, lab supplies, drug supplies as appropriate. This may require a certain amount of lifting in the course of the packing/unpacking courier boxes and sufficient equipment and training will be provided.
- To assist project teams with trial progress tracking by updating the Clinical Trial Management systems.
- To be familiar with internal tracking systems, as required.
- To assist in the tracking and distribution of safety reports.
- To organise project team meetings and investigator meetings and take minutes, as required.
- To co-ordinate document translation.
- To assist in the preparation of presentations.
Qualifications and Experience
- University degree or equivalent or relevant proven industry experience.
- Demonstrated organisational skills
- Computer literacy eg MS Word, Excel and Powerpoint.
- Good communication skills.
Benefits
With this position comes an attractive salary that you would associate with a world leader.
Key Words
Clinical Trial Assistant, CTA, Clinical Research, Study Management, Research, Pharmaceutical, CRO, Clinical Trials, Career, Medical, Clinical, Clinical Management, Job, Recruitment, Hampshire.
This position will be based in Hampshire.
You must be logged in to apply for this position. Log in using the form on the right, at the top of the page beneath the logo, or click here to register.
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