Explore exciting Research Associate positions. These roles involve conducting experiments, analyzing data, and contributing to scientific publications. Research Associates work in diverse fields, including 3,765 Research Associate jobs in the United Kingdom
Clinical Research Associate
Posted today
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Clinical Research Associate (CRA) – Hybrid – London Region
RBW Consulting is excited to announce an opportunity on behalf of a small CRO client we are partnered with. This company focuses on UK-based studies and site visits are regionally based around the London area.
This opportunity offers exposure to varied therapy areas, manageable site visits, and the chance to develop beyond traditional monitoring responsibilities.
The Role
You’ll be working on a broad portfolio of studies, from initiation through to close out, across multiple therapy areas including respiratory and emerging fields. This hybrid position involves monitoring sites (primarily in and around London) and attending the office approximately twice per month.
Key responsibilities include:
- Monitoring visits at UK trial sites
- Setting up, managing, and maintaining eTMFs
- Ensuring delivery of studies within budget and timelines
- Liaising with sponsors, vendors, and internal teams to maintain project oversight
- Supporting colleagues through training and mentoring in areas of expertise
- Contributing to project, client, and team meetings
What We’re Looking For
- At least 1 year experience as a CRA (can consider candidates with academic or industry experience)
- A proactive approach with the flexibility to handle multiple priorities in a dynamic environment
The Offer
- Salary range: £40,000–£47,000 , with potential annual increases
- 25 days annual leave plus standard benefits
- Hybrid working model (office attendance twice per month)
- Opportunities for professional growth, with development into Senior CRA or Project Management roles
This role is ideal for CRAs who enjoy a mix of independence and collaboration, and who want to be part of an organisation that values quality, career growth, and work-life balance.
To apply:
Please click ‘apply’ or contact Joe Pearce for any further information
About RBW Consulting
RBW Consulting is a life sciences talent & strategic consultancy with purpose, delivered through what we call Human Intelligence. We help life sciences businesses change the world by giving them the people, insight & networks to innovate and scale. We are proud of our role in helping companies deliver better health and wellbeing outcomes for patients We give back by playing an active role in funding initiatives that change lives We’ve created a culture rooted in support, transparency and mutual commitment. We lead with our values from the inside; empowering and investing in our people is more important than short-term commercial gain.
We are an equal opportunities Recruitment Business and Agency
RBW Consulting is an equal opportunity workplace. We prioritize talent (both current and potential) over resumes, challenge the status quo, and value people as our most important asset. We do not discriminate on the basis of race, ethnicity, colour, sex, gender identity or expression, sexual orientation, religion, age, marital status, visible or invisible disability, medical condition, national origin, veteran status, or any other protected status. We strive to be a diverse workforce that is representative at all levels and are committed to building a team that represents a variety of backgrounds, perspectives, and skills.
Clinical Research Associate
Posted today
Job Viewed
Job Description
Clinical Research Associate (CRA) – Hybrid – London Region
RBW Consulting is excited to announce an opportunity on behalf of a small CRO client we are partnered with. This company focuses on UK-based studies and site visits are regionally based around the London area.
This opportunity offers exposure to varied therapy areas, manageable site visits, and the chance to develop beyond traditional monitoring responsibilities.
The Role
You’ll be working on a broad portfolio of studies, from initiation through to close out, across multiple therapy areas including respiratory and emerging fields. This hybrid position involves monitoring sites (primarily in and around London) and attending the office approximately twice per month.
Key responsibilities include:
- Monitoring visits at UK trial sites
- Setting up, managing, and maintaining eTMFs
- Ensuring delivery of studies within budget and timelines
- Liaising with sponsors, vendors, and internal teams to maintain project oversight
- Supporting colleagues through training and mentoring in areas of expertise
- Contributing to project, client, and team meetings
What We’re Looking For
- At least 1 year experience as a CRA (can consider candidates with academic or industry experience)
- A proactive approach with the flexibility to handle multiple priorities in a dynamic environment
The Offer
- Salary range: £40,000–£47,000 , with potential annual increases
- 25 days annual leave plus standard benefits
- Hybrid working model (office attendance twice per month)
- Opportunities for professional growth, with development into Senior CRA or Project Management roles
This role is ideal for CRAs who enjoy a mix of independence and collaboration, and who want to be part of an organisation that values quality, career growth, and work-life balance.
To apply:
Please click ‘apply’ or contact Joe Pearce for any further information
About RBW Consulting
RBW Consulting is a life sciences talent & strategic consultancy with purpose, delivered through what we call Human Intelligence. We help life sciences businesses change the world by giving them the people, insight & networks to innovate and scale. We are proud of our role in helping companies deliver better health and wellbeing outcomes for patients We give back by playing an active role in funding initiatives that change lives We’ve created a culture rooted in support, transparency and mutual commitment. We lead with our values from the inside; empowering and investing in our people is more important than short-term commercial gain.
We are an equal opportunities Recruitment Business and Agency
RBW Consulting is an equal opportunity workplace. We prioritize talent (both current and potential) over resumes, challenge the status quo, and value people as our most important asset. We do not discriminate on the basis of race, ethnicity, colour, sex, gender identity or expression, sexual orientation, religion, age, marital status, visible or invisible disability, medical condition, national origin, veteran status, or any other protected status. We strive to be a diverse workforce that is representative at all levels and are committed to building a team that represents a variety of backgrounds, perspectives, and skills.
Clinical Research Associate
Posted today
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Job Description
Clinical Research Associate
Posted today
Job Viewed
Job Description
Clinical Research Associate
Posted today
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Job Description
Clinical Research Associate
Posted today
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Senior Research Associate
Posted 5 days ago
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Job Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
+ Based at DJS Antibodies in Headington, Oxford
+ Reporting to Senior Scientist II
At DJS Antibodies, we aspire to create the next generation of antibody therapeutics and in doing so improving the prognosis for patients with life-changing immunological diseases and cancers. As a biotech company within AbbVie, we combine the agility, team spirit and scientific focus of a biotech with the reach and vision of a global pharmaceutical company. We have developed a number of drug candidates to date and are looking forward to growing our portfolio to have the biggest impact on patients' lives.
A critical part of achieving our vision is working with fantastic people, and as such we are looking for an enthusiastic and talented Research Assistant/Senior Research Assistant to join the team. For this role, candidates should be excited about working in a small, dynamic team; always keen to get involved with all aspects of research at DJS; be a team player; have a high level of skill and passion for in vivo work. This position represents an excellent opportunity for someone looking to begin or solidify their career within an industry laboratory research environment working on innovative projects whilst developing a variety of new skills.
Job Overview
The successful candidate will work closely with the PPL holder to plan experiments such as immunisation to generate antibody responses and testing the biological effects of lead antibodies that we have discovered. They will be responsible for preparing biological materials for these experiments, performing the required in vivo techniques and analysing the results. They will also have the opportunity to carry out laboratory experiments utilising molecular biology, cell culture, antibody production and various assay techniques to support the DJS discovery activities as a key member of the team. In addition to on-site laboratory work they will be required to work with live rodent models and animal derived tissues in the off-site facility for up to 50% of time.
At DJS, we want to foster innovative scientists performing cutting-edge science. A successful applicant will be a practical person who is organised, pays attention to detail, and efficiently gets the job done. Previous experience in a range of analytical techniques is preferred but is not essential as training will be provided.
They will have many opportunities for scientific career development and improvement of their knowledge of a world leading R&D/drug development pipeline and the broader business both at DJS and within AbbVie.
Successful applicant's key responsibilities
+ Bringing energy, enthusiasm and positivity to the company
+ Animal model husbandry
+ Performing experiments with live animals
+ Collection of animal derived tissues
+ Maintenance of cell cultures
+ Transient protein expression with mammalian cell lines
+ Work as a key member of the DJS discovery team
+ Performing critical laboratory experiments and analysing the data to contribute to strategic decision making within DJS discovery
+ Keeping up to date with developments in the literature in relation to technical aspects of drug discovery technologies
+ Day-to-day laboratory management as part of the team e.g. maintaining a safe and clean working laboratory environment, re-ordering laboratory consumables
+ Establishing and maintaining quality sample archives
+ Gathering, analysing and presenting data from a variety of sources to the wider team and organization
+ Critical and impartial review of self and peer generated laboratory data
+ Maintenance of laboratory experimental records
+ Follow established procedures, protocols and study plans and recommend changes for refinement. Adhere to regulatory requirements.
Qualifications
+ A BSc of 2:1 level or higher with intercalated year in industrial/academic research and/or an MSc/MRes or higher degree with significant lab experience in a relevant discipline (such as Biology, Biochemistry, pathology, cell biology or Natural Sciences)
+ A current UK PIL AB licence (or equivalent) with 5 years experience in working with animal models.
+ Proven competencies in in vivo procedures in experimental rodents
+ For example: intravenous, intramuscular, intrapertitoneal, sub-cutaneous injections, blood sampling, schedule 1 methods, use of anesthetics.
+ It will be a requirement to pass a 6-month probationary period at DJS that the candidate is declared competent in all relevant techniques by the vivarium staff.
+ Enthusiasm for and commitment to drug discovery and drug development research
+ Proven recent experience in
+ Performing in vivo experiments in experimental rodents
+ Mammalian cell culture
+ Molecular and biochemical techniques (such as; bacterial cell culture; flow cytometry; PCR; ELISA; protein expression and purification)
+ Evidence of excellent organizational and interpersonal skills including
+ Ability to work both independently and as part of a team
+ Ability to work efficiently with strong attention to detail
+ Ability to build effective working relationships
+ Laboratory method development
+ Ability to work flexible hours when required
+ Proven written and oral communicative ability
+ Problem-solving skills
+ Strong IT skills
+ Desirable skills
+ + Experience with running experimental models of inflammation in rodents
+ PIL C licence and experience with surgical techniques. Good knowledge of statistics
Additional Information
About DJS Antibodies
At DJS Antibodies as part of AbbVie our ambition is to contribute world class novel antibody therapeutics for the treatment of severe diseases into AbbVies clinical pipeline. Our proprietary antibody discovery technology enables us to discover first in class antibodies to the key drivers of disease that have, until now, been intractable to drug discovery such as GPCR's and other complex membrane and soluble targets.
Working at DJS will involve coming into a stimulating and entrepreneurial work environment with excellent exposure to industry-leading experts. Being part of a small team means that you will be exposed to all aspects of R&D and the broader business. You will benefit from working with a great team, a competitive remuneration package and significant opportunities for career development.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
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Clinical Research Associate
Posted 10 days ago
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Job Description
Job Title: Junior Clinical Research Associate (CRA)
Location: London, UK (Field-based with regular site visits)
Employment Type: Full-time
About the Role:
We are seeking a motivated Junior Clinical Research Associate (CRA) with a minimum of 2 years of independent monitoring experience to join our London-based team. The successful candidate will play a vital role in ensuring the quality and integrity of clinical trials across multiple therapeutic areas. You will conduct 4–6 monitoring visits per month , providing oversight of study sites while maintaining compliance with ICH-GCP, local regulations, and study protocols.
Key Responsibilities:
- Perform routine monitoring visits (site initiation, interim, and close-out) across assigned sites in London and surrounding regions.
- Ensure adherence to protocol, ICH-GCP, and applicable regulatory requirements.
- Verify accuracy and completeness of case report forms (CRFs) against source data.
- Identify and resolve data discrepancies and protocol deviations in collaboration with site staff.
- Maintain effective communication with investigators, site personnel, and internal study teams.
- Prepare and submit timely monitoring reports and follow-up documentation.
- Support investigators and sites in resolving queries and ensuring readiness for audits and inspections.
- Contribute to trial start-up activities when required (e.g., site feasibility, essential document collection).
Requirements:
- Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field.
- Minimum 2 years of independent monitoring experience within a CRO, pharmaceutical, or biotech environment.
- Strong knowledge of ICH-GCP and UK clinical trial regulations.
- Excellent organizational and time management skills with the ability to manage multiple sites.
- Willingness to travel frequently (4–6 site visits per month).
- Strong interpersonal and communication skills, both written and verbal.
What We Offer:
- Competitive salary and benefits package.
- Professional development opportunities within a growing clinical operations team.
- Exposure to diverse therapeutic areas and phases of clinical development.
- Supportive work environment with mentorship from senior CRAs.
Clinical Research Associate
Posted 10 days ago
Job Viewed
Job Description
Job Title: Junior Clinical Research Associate (CRA)
Location: London, UK (Field-based with regular site visits)
Employment Type: Full-time
About the Role:
We are seeking a motivated Junior Clinical Research Associate (CRA) with a minimum of 2 years of independent monitoring experience to join our London-based team. The successful candidate will play a vital role in ensuring the quality and integrity of clinical trials across multiple therapeutic areas. You will conduct 4–6 monitoring visits per month , providing oversight of study sites while maintaining compliance with ICH-GCP, local regulations, and study protocols.
Key Responsibilities:
- Perform routine monitoring visits (site initiation, interim, and close-out) across assigned sites in London and surrounding regions.
- Ensure adherence to protocol, ICH-GCP, and applicable regulatory requirements.
- Verify accuracy and completeness of case report forms (CRFs) against source data.
- Identify and resolve data discrepancies and protocol deviations in collaboration with site staff.
- Maintain effective communication with investigators, site personnel, and internal study teams.
- Prepare and submit timely monitoring reports and follow-up documentation.
- Support investigators and sites in resolving queries and ensuring readiness for audits and inspections.
- Contribute to trial start-up activities when required (e.g., site feasibility, essential document collection).
Requirements:
- Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field.
- Minimum 2 years of independent monitoring experience within a CRO, pharmaceutical, or biotech environment.
- Strong knowledge of ICH-GCP and UK clinical trial regulations.
- Excellent organizational and time management skills with the ability to manage multiple sites.
- Willingness to travel frequently (4–6 site visits per month).
- Strong interpersonal and communication skills, both written and verbal.
What We Offer:
- Competitive salary and benefits package.
- Professional development opportunities within a growing clinical operations team.
- Exposure to diverse therapeutic areas and phases of clinical development.
- Supportive work environment with mentorship from senior CRAs.
Clinical Research Associate
Posted 5 days ago
Job Viewed
Job Description
Responsibilities:
- Monitor clinical trial sites to ensure adherence to protocol, GCP, and regulatory requirements.
- Verify the accuracy, completeness, and consistency of clinical data.
- Manage study-related documentation and regulatory submissions.
- Communicate effectively with investigators, site staff, and study sponsors.
- Identify, evaluate, and select potential clinical trial sites.
- Train site personnel on study protocols and procedures.
- Perform site initiation, interim monitoring, and close-out visits.
- Address and resolve site-level issues and discrepancies.
- Ensure timely reporting of adverse events and protocol deviations.
- Contribute to the development of clinical trial protocols and study plans.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Previous experience as a Clinical Research Associate or in a similar clinical research role.
- In-depth knowledge of Good Clinical Practice (GCP), ICH guidelines, and relevant regulatory requirements.
- Familiarity with clinical trial monitoring procedures and data management systems.
- Excellent organizational and time management skills.
- Strong attention to detail and accuracy.
- Effective written and verbal communication skills.
- Ability to travel to clinical sites as required.
- Proficiency in Microsoft Office Suite and clinical trial management software.
- A proactive approach to problem-solving and a commitment to patient safety.