Clinical Trials Sub-Investigator – Bristol – Up to £65,000 DoE + Benefits
The Company
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An emerging CRO, specialising in treatment for mental health services. Working with clinical trials such as Migraine, ADHD, Dementia and Brain Injuries.
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A presence in the UK and the US, looking to grow in both locations.
The Role
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Perform studies in accordance with ICH GCP guidelines
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Signing Investigator Agreements to confirm acceptance and willingness to comply with study protocols
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Maintain study records and investigation into any adverse effects and changes to medications
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Assist in pre-screening and recruitment of participants into the studies
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Carry out any specific administrative duties required for individual studies
You
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Valid GMC registration with no limitations to practice.
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2+ years’ experience within a clinical trials setting.
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Ideally will have membership through qualification with MRCP
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Strong clinical competency
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Desire to progress in a research setting
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Great communication skills and a good bedside manner
What should you do next?
A guaranteed development opportunity for somebody looking to grow their career within the clinical trials field, focusing on neuroscience specialities, an ever-growing therapeutic area in the world of research.
To discuss this role further or to find out about other roles I’m currently working on, please get in touch or hit apply to submit your current CV.
Unless otherwise stated, if applying for a job within the UK or European Union, you must ensure that you are already authorised to work there.
Carrot Recruitment acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.
We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, colour, sex, age, national origin, religion, sexual orientation, gender identity and/or expression.
If there are any arrangements or adjustments, we can make to assist you at interview then please let us know and we'll be more than happy to assist.