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Research Assistant in Biomedical Science jobs
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- O4 ResearchBradford-on-Avon
- Company pension
- Competence in venepuncture and blood sample processing.
- Previous experience delivering participant-facing clinical research visits.
- Bishop Wordsworth's SchoolSalisbury SP1 2ED
- Company pension
- On-site gym
- Cycle to work scheme
- A genuine interest in science and a willingness to learn.
- This is an excellent opportunity for someone with an interest in science who is keen to learn and…
- Mintech-BioNottingham
- Providing support and advice in biomaterial formulations, design, and development.
- Experience in synthetic chemistry and working with polymers, proteins,…
- Mintech-BioNottingham
- Providing support and advice in biomaterial formulations, design, and development.
- Experience in synthetic chemistry and working with polymers, proteins,…
Scientist - Early Career
Often replies in 1 dayMomentous TherapeuticsHarston- Life insurance
- Company pension
- Private medical insurance
- Company events
- Casual dress
- On-site parking
- A degree in Cell Biology, Molecular Biology, Biochemistry, or a related life science discipline would be desirable.
- Experience in market research preferred, ideally in the medical/healthcare field.
- The candidate must have the ability to manage multiple research projects…
- SAVALondon EC1M
- Experience working in regulated environments, medical devices preferred.
- 3 to 4+ years of experience in clinical operations, ideally within medical devices.
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- Greater Manchester Mental Health NHS Foundation...Manchester M40 5BP
- The post holder will be expected to have proven and substantial experience in conducting research; for example, by having previously assisted in the running of…
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- Wrightington, Wigan and Leigh Teaching Hospitals...Wigan WN6 9EP
- Supervising and support junior research staff.
- Recording research data accurately and keeping data secure.
- The Research Delivery Team at Wrightington, Wigan and…
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- GlaxoSmithKlineLondon
- Language requirement: Written and spoken fluency in English.
- Education required: BSc degree from an accredited college/university, preferably in medical or…
- The Christie NHS Foundation TrustManchester M20 4BX
- The post will offer experience in cutting edge research in personalised medicine and immunotherapy, Early Phase trials, and experience in managing complex cases…
- Thermo Fisher ScientificRemote
- Master’s degree in science discipline, with at least 5 years’ experience in a relevant field; or.
- Assist PIs in preparing clients for regulatory meetings.
- University College London Hospitals NHS Foundation...London WC1N 3BG
- Administration and running of in-house, national and international late phase neurology clinical trials.
- Our vision is to deliver top-quality patient care,…
- CytivaPortsmouth
- Review job requests, relevant safety data and fully understand testing requirements in accordance with laboratory SOPs.
- Conversant with PC based programmes.
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- CytivaPortsmouth
- Generation of test data to specified protocols in support of New Product Development and Manufacturing.
- Review job requests, relevant safety data and fully…
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- PharmaronLiverpool
- BSc/MSc (or equivalent) in related field.
- Drive activities in compliance with cGMP and Pharmaron quality systems.
- Knowledge and previous Molecular Biology.
Job Post Details
Clinical Research Practitioner
Bradford-on-Avon
£37,000 - £43,000 a year
-
Fixed term contract, Part-time
Clinical Research Practitioner
Job details
£37,000 - £43,000 a year
Company pension
Fixed term contract, Part-time
Bradford-on-Avon
Full job description
Job Overview
O4 Research Ltd is recruiting a part-time (2 days a week) experienced Clinical Research Practitioner to support clinical research delivery at a GP practice in Bradford-on-Avon
This is a hands-on, participant-facing role combining clinical procedures, study visit coordination and data management. You will work closely with the practice’s Principal Investigator and clinical team, with support from O4’s OnSite team.
The Role
- You will coordinate and deliver study visits, independently undertaking delegated procedures within your training and demonstrated competence. Your responsibilities will include:
- Supporting participant identification, screening, recruitment and retention.
- Scheduling and preparing study visits within protocol-required timelines.
- Undertaking venepuncture, blood sample processing, clinical observations and other study assessments.
- Supporting the informed consent process and obtaining consent where appropriately trained and authorised.
- Collecting, processing, storing and arranging shipment of biological samples.
- Providing clear information and ongoing support to participants.
- Recognising and promptly escalating safety concerns to the investigator.
- Maintaining accurate study records, entering data and resolving queries.
- Maintaining study documentation and supplies and supporting monitoring visits.
About You
Essential requirements
- Previous experience delivering participant-facing clinical research visits
- Competence in venepuncture and blood sample processing
- Experience undertaking and documenting routine clinical assessments
- Ability to manage delegated study activities with minimal day-to-day supervision, following study-specific training
- Working knowledge of Good Clinical Practice and participant confidentiality
- Experience with study documentation and records, electronic data entry and query resolution
- Excellent organisation, attention to detail and communication skills
- A relevant healthcare, life sciences or research qualification, or equivalent relevant training and experience
Desirable
- At least two years’ relevant clinical research delivery experience
- Experience in a GP practice or primary care setting
- Familiarity with EMIS or SystmOne
- Relevant endocrinology therapeutic area experience
- Registration on the AHCS Accredited Register for Clinical Research Practitioners
Key Competencies
- Strong organisation, time management and attention to detail
- Clear, sensitive communication and effective teamwork
- Ability to work independently, solve problems and escalate appropriately
- Professional, approachable and participant-focused manner
NOTE: Expected contract length is 12 months with the potential for extension.
Pay: £37,000.00-£43,000.00 per year
Benefits:
- Company pension
Application question(s):
- What is the highest level of education you have completed?
- How many years of Clinical Research experience do you have?
- Do you have a working knowledge of ICH GCP, clinical trials and the drug development process?
- This is a part-time role, 2 days a week, and you will be required to be on site for both days, does that suit you?
Work authorisation:
- United Kingdom (required)
Work Location: In person
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