180 Applied Research jobs in the United Kingdom

Research Associate (Applied Workflow)

Cambridge, Eastern Nuclera

Posted 4 days ago

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Job Description

Permanent

Nuclera is a venture-backed biotech company headquartered in Cambridge, UK with significant operations in Boston, USA. Nuclera’s mission is to accelerate discovery by enabling rapid, easy access to functional proteins essential for drug discovery research. Our eProtein Discovery™ benchtop system accelerates protein expression and purification optimization in research labs.

This is a lab-based role within a group central to Nuclera’s technology development program that will be conducted in close collaboration with colleagues from other groups in the company. A key aspect of this role will be to contribute to the customer collaborations and marketing collateral through demonstration of new capabilities of our platform.

The role would suit a candidate with excellent communication and organization skills, with a drive for working in a fast-paced biotech environment and a track record of execution and teamwork. Experience in molecular biology, protein expression and characterisation is essential. 

This role will be based in the Cambridge, UK site and is on-site in the lab with some flexibility for home working (up to 1 day per week). 

About the role

  • Follow SOPs to independently execute and analyze experiments on the eProtein Discovery System to contribute to customer collaborations.
  • Design, execute, and troubleshoot protein activity assays with guidance from senior members of the group.
  • Work on multiple protein projects in parallel.
  • Actively engage in scientific discussion within the group and across groups to contribute to robust product development.
  • Report results in a timely manner and maintain good laboratory practices.

Requirements

Essential:

  • BS/MSc in protein biophysics, biochemistry, molecular biology or a related area, with 2-4 years’ (for BS) and 1 years’ (for MSc) industry experience
  • Track record of delivering robust data and high-quality results within tight timelines
  • Experience with common molecular biology techniques, including PCR and agarose gel electrophoresis
  • Experience with common protein expression and purification techniques, including affinity purification, SDS-PAGE gel electrophoresis, protein quantification
  • A collaborative team player with a positive can-do attitude
  • Strong problem solving capabilities, clear communication and presentation skills
  • Self-motivated interest in Nuclera’s technology.

Desirable:

  • Previous working experience in the pharmaceutical, CRO, and/or biotechnology industry would be advantageous.
  • Understanding the principles of cell-free protein synthesis technologies
  • Experience in protein engineering and structure-guided design of protein variants for stability, activity, or yield.
  • Some knowledge of protein assays, characterisation and functional properties (e.g. solubility, aggregation properties, activity)

Benefits

What we offer:

In addition to competitive salaries, we offer a range of benefits including:

  • Company bonus scheme of 5%
  • Share option incentive scheme 
  • Life insurance 
  • Private medical insurance and cash plan 
  • 25 days' annual leave + Bank Holidays 
  • Enhanced employer's pension contributions 
  • Enhanced maternity and paternity Leave 
  • Investment in professional development and learning 
  • Fresh fruit, tea, coffee, and snacks in the office 
  • Organised summer events for staff
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Research Associate

Staffordshire, West Midlands CK Group- Science, Clinical and Technical

Posted 3 days ago

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Job Description

permanent
CK Group are recruiting for an R&D Research Associate to join a chemicals manufacturing company, at their site based in Stoke, on a full time, permanent basis.



The Company:

Our client is a leader in the global manufacture of their specialty materials. Developing and manufacturing a range of pigments and nanomaterials, they now have an opportunity for a R&D Research Associate.



Location:

The R&D Researcher will be based at the company's site in Stoke, easily commutable from surrounding areas.



R&D Research Associate:



Your main duties will be:

  • Creating new ideas for novel advanced materials
  • Synthesizing new materials for various technical applications like window films, inks, conductive coatings, Laser Marking, Dispersions
  • Upscaling laboratory procedures into pilot plant scale
  • Solving technical challenges in new product development
  • Working collaboratively with other team members and customers
  • Providing customer technical support
  • Analysing performance of competitive products in customer applications
  • Demonstrating performance of products in various applications


Your Background:



The ideal candidate for this role will have the following skills and experience:

  • MSc or PhD in Inorganic Chemistry, Material Science or related discipline
  • Preferably knowledge in one of the fields: inks, coatings, polymer processing, Laser Marking, Nanodispersions
  • Systematic approach to tasks
  • Roll-up sleeves, initiative, and self-motivating mentality
  • Creativity and innovative approach to tasks
Apply:

Entitlement to work in the UK is essential. Please quote job reference (Apply online only) in all correspondence.

INDCH



If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
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Research Associate

ST1 Stoke on Trent, West Midlands CK Group- Science, Clinical and Technical

Posted 3 days ago

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Job Description

full time
CK Group are recruiting for an R&D Research Associate to join a chemicals manufacturing company, at their site based in Stoke, on a full time, permanent basis.



The Company:

Our client is a leader in the global manufacture of their specialty materials. Developing and manufacturing a range of pigments and nanomaterials, they now have an opportunity for a R&D Research Associate.



Location:

The R&D Researcher will be based at the company's site in Stoke, easily commutable from surrounding areas.



R&D Research Associate:



Your main duties will be:

  • Creating new ideas for novel advanced materials
  • Synthesizing new materials for various technical applications like window films, inks, conductive coatings, Laser Marking, Dispersions
  • Upscaling laboratory procedures into pilot plant scale
  • Solving technical challenges in new product development
  • Working collaboratively with other team members and customers
  • Providing customer technical support
  • Analysing performance of competitive products in customer applications
  • Demonstrating performance of products in various applications


Your Background:



The ideal candidate for this role will have the following skills and experience:

  • MSc or PhD in Inorganic Chemistry, Material Science or related discipline
  • Preferably knowledge in one of the fields: inks, coatings, polymer processing, Laser Marking, Nanodispersions
  • Systematic approach to tasks
  • Roll-up sleeves, initiative, and self-motivating mentality
  • Creativity and innovative approach to tasks
Apply:

Entitlement to work in the UK is essential. Please quote job reference (Apply online only) in all correspondence.

INDCH



If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
This advertiser has chosen not to accept applicants from your region.

Research Associate GLOW

LE11 3TT Loughborough, East Midlands Loughborough University

Posted 4 days ago

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Job Description

Job Title: Research Associate GLOWJob Reference: REQ250548Date Posted: Fri, 27 Jun 2025 00:00:00 GMTApplication Closing Date: Wed, 30 Jul 2025 00:00:00 GMTLocation: LoughboroughPackage: Specialist and Supporting Academic Research grade 6 from £35116

School of Social Sciences & Humanities (SSH)

Part time: (16 hours per week)

Fixed Term Contract:  from 1 September 2025 to 30 April 2026.

Hybrid work: mostly online, with some occasional on-site work.

We're on the lookout for a postdoctoral research associate who will join the GLOW team.

Much public good could be derived from the analysis of government records, particularly records in digital form. Yet, access to these data is extremely difficult . Archival emails and other born-digital records are rarely accessible to users for many reasons - including confidentiality, privacy, national security, copyright, technological constraints, and a lack of organisation.

The GLOW project will connect government professionals with Computer Scientists, Digital Humanists and professionals in the GLAM sector (Galleries, Libraries, Archives and Museums) in the UK and USA – in order to unlock government archives with AI .

The project is led by Professor Lise Jaillant, Professor of Digital Cultural Heritage. The researcher will work closely with the PI to deliver this project.

Your primary responsibilities will be to conduct qualitative research including data collection, analysis and management, to manage communications with the stakeholders involved in the project, and to contribute to the organisation and delivery of the project events.

Key Requirements:

  • You’ll have a PhD in social sciences or humanities (or near completion)
  • You’l bring expertise in qualitative data collection and analysis
  • You l have experience of authoring original work for academic journal papers
  • You l be able to organise complex events involving multiple stakeholders

Why should you apply?

With a huge amount of variety in the role, there is an opportunity for you to develop and continually grow.

If this role sounds of interest, we love to hear from you.

Informal enquiries should be directed to Professor Lise Jaillant, via email to

For more information refer to theJob Description and Person Specification .

Closing Date: 30th July 2025

Interview Date: anticipated to be the week of 25th August 2025

Our Benefits

  • Generous annual leave allowance up to 44 days (inclusive of Bank Holidays & University closure days)
  • Competitive pension schemes
  • A range of childcare support initiatives and benefits including childcare vouchers; on-site university nursery (with salary sacrifice scheme); and holiday play schemes.
  • We offer a range of family friendly, inclusive employment policies.
  • BUPA Cash Plan (100 scheme)
  • Employee Assistance Programme
  • Season ticker loan scheme
  • On campus parking with charging points for electric vehicles
  • Fantastic range of sports facilities and preferential membership packages available
This advertiser has chosen not to accept applicants from your region.

Research Associate II

Glasgow, Scotland ThermoFisher Scientific

Posted 2 days ago

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Job Description

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - To enable our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies.
Alongside clinical research through our PPD® clinical research portfolio, our work in Accelerated Enrollment Solutions optimizes each step of the patient journey in clinical trials, such as securing sites and recruiting patients, allowing for more patients to participate in clinical research. Your determination to put patients at the heart of every decision will improve health outcomes that people and communities depend on - now and in the future.
**Are you passionate about improving patient's lives for the better?**
We are currently looking to recruit a Research Associate for our Synexus Clinical Research site in Glasgow, United Kingdom.
Working days, Monday to Friday, 37 hours a week, the main priority will always be patient safety. Provides general support to technical procedures with a range of complexity, including phlebotomy. Collects study-specific data by performing technical and non-technical procedures and interacting with patients. May also assist with the verification of patient data and collecting source documentation to complete the medical history. Monitors and ensures overall compliance at the site.
**Key responsibilities for a Research Associate are as follows:**
+ May perform technical procedures running patient clinics including vital signs, Fibroscan, height, weight, Electrocardiogram etc. Fully informs patients about the tests to be conducted and guides patients in the requirements of the trial.
+ May perform Phlebotomy tests.
+ Performs non-technical procedures, including urine collection, subject walks and safety monitoring.
+ Under the general supervision of a licensed physician, may conduct the education, evaluation, treatment and follow-up of sleep disorders for clinic patients by following sleep laboratory operating procedures, applying electrodes and sensors to ensure the collection of appropriate data of the sleep testing process.
+ Prepares and calibrates equipment for testing to ensure proper functioning.
+ Interacts regularly with patients during study visits in order to perform study related procedures.
+ Undertakes screening tests in accordance with protocol requirements.
+ Assists in the lab, sample processing and/or liaise with laboratories.
+ Manages and/or completes ordering of clinical supplies.
+ May assist with or oversee the maintenance of accurate freezer logs, specimen labelling and other documentation.
+ May take consent if permitted according to country regulations.
+ Reports Quality Incidents and participates in the investigation and resolution.
+ Provides administrative support as needed.
+ Ensures adherence to COP's, SOP's, GCP and local regulations.
+ Provides training to new staff.
Note: Some tasks listed above only to be conducted as per country regulations and with relevant valid qualifications/ certification or supervision.
**To be considered for this exciting opportunity you will require the following skills and experience:**
+ Good medical terminology and ability to perform conducting of vital signs
+ Strong understanding of Good Clinical Practices (GCP), with ability to learn and maintain a good working knowledge of FDA regulations and company/client SOPs and WPDs
+ Strong organizational skills and flexibility to manage workload and meet changing timelines, handling multiple tasks efficiently and effectively
+ Thorough attention to detail to ensure accuracy and efficiency in data entry
+ Strong interpersonal/customer service skills, positive attitude and good oral and written communication
+ Capable of working in a team or independently
+ Strong English language and grammar skills
+ Strong computer skills, including proficiency in MS Office (Word, Excel, and PowerPoint) and basic understanding of clinical trial database systems
+ Strong analytical and data management skills to effectively analyze data/systems to ensure accuracy and efficiency
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
This advertiser has chosen not to accept applicants from your region.

Research Associate II

Birmingham, West Midlands ThermoFisher Scientific

Posted 2 days ago

Job Viewed

Tap Again To Close

Job Description

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - To enable our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies.
Alongside clinical research through our PPD® clinical research portfolio, our work in Accelerated Enrollment Solutions optimizes each step of the patient journey in clinical trials, such as securing sites and recruiting patients, allowing for more patients to participate in clinical research. Your determination to put patients at the heart of every decision will improve health outcomes that people and communities depend on - now and in the future.
**Are you passionate about improving patient's lives for the better?**
We are currently looking to recruit a Research Associate II for our Synexus Clinical Research site in Birmingham, United Kingdom.
Working days, Monday to Friday, 37 hours a week, the main priority will always be patient safety. Provides general support to technical procedures with a range of complexity, including phlebotomy. Collects study-specific data by performing technical and non-technical procedures and interacting with patients. May also assist with the verification of patient data and collecting source documentation to complete the medical history. Monitors and ensures overall compliance at the site.
**Key responsibilities for a Research Associate are as follows:**
+ May perform technical procedures running patient clinics including vital signs, Fibroscan, height, weight, Electrocardiogram etc. Fully informs patients about the tests to be conducted and guides patients in the requirements of the trial.
+ May perform Phlebotomy tests.
+ Performs non-technical procedures, including urine collection, subject walks and safety monitoring.
+ Under the general supervision of a licensed physician, may conduct the education, evaluation, treatment and follow-up of sleep disorders for clinic patients by following sleep laboratory operating procedures, applying electrodes and sensors to ensure the collection of appropriate data of the sleep testing process.
+ Prepares and calibrates equipment for testing to ensure proper functioning.
+ Interacts regularly with patients during study visits in order to perform study related procedures.
+ Undertakes screening tests in accordance with protocol requirements.
+ Assists in the lab, sample processing and/or liaise with laboratories.
+ Manages and/or completes ordering of clinical supplies.
+ May assist with or oversee the maintenance of accurate freezer logs, specimen labelling and other documentation.
+ May take consent if permitted according to country regulations.
+ Reports Quality Incidents and participates in the investigation and resolution.
+ Provides administrative support as needed.
+ Ensures adherence to COP's, SOP's, GCP and local regulations.
+ Provides training to new staff.
Note: Some tasks listed above only to be conducted as per country regulations and with relevant valid qualifications/ certification or supervision.
**To be considered for this exciting opportunity you will require the following skills and experience:**
+ Good medical terminology and ability to perform conducting of vital signs
+ Strong understanding of Good Clinical Practices (GCP), with ability to learn and maintain a good working knowledge of FDA regulations and company/client SOPs and WPDs
+ Strong organizational skills and flexibility to manage workload and meet changing timelines, handling multiple tasks efficiently and effectively
+ Thorough attention to detail to ensure accuracy and efficiency in data entry
+ Strong interpersonal/customer service skills, positive attitude and good oral and written communication
+ Capable of working in a team or independently
+ Strong English language and grammar skills
+ Strong computer skills, including proficiency in MS Office (Word, Excel, and PowerPoint) and basic understanding of clinical trial database systems
+ Strong analytical and data management skills to effectively analyze data/systems to ensure accuracy and efficiency
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
This advertiser has chosen not to accept applicants from your region.

Research Associate Wellcome Project

LE11 3TT Loughborough, East Midlands Loughborough University

Posted 4 days ago

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Job Description

Job Title: Research Associate Wellcome ProjectJob Reference: REQ250580Date Posted: Fri, 11 Jul 2025 00:00:00 GMTApplication Closing Date: Wed, 30 Jul 2025 00:00:00 GMTLocation: LoughboroughPackage: Specialist and Supporting Academic Research grade 6 from £35116 to £42882.

Wolfson School of Mechanical Electrical and Manufacturing Engineering

Full time, Fixed Term for 12 months

We are seeking a highly motivated, results-oriented, self-starter who thrives on increasing levels of responsibility. Applicants should have completed -or be very close to completion of- a PhD in a relevant subject such as 3D in-vitro model systems, microfluidics, tissue engineering, or cellular biology and have interest in applying this knowledge to ageing research. 

Alongside your core tasks, you will be encouraged and supported in establishing collaborative research in ageing research, and to engage in collaborations locally, nationally, and internationally. We are committed to supporting your career development with mentoring and training opportunities to enhance your skills and experience.

For more information refer to the Job Description and Person Specification.

Informal Enquiries

Can be directed to Alexandra Stolzing

Application closing date : 30 July 2025

Our Benefits

  • Generous annual leave allowance up to 44 days (inclusive of Bank Holidays & University closure days)
  • Competitive pension schemes
  • A range of childcare support initiatives and benefits including childcare vouchers; on-site university nursery (with salary sacrifice scheme); and holiday play schemes.
  • We offer a range of family friendly, inclusive employment policies.
  • BUPA Cash Plan (100 scheme)
  • Employee Assistance Programme
  • Season ticket loan scheme
  • On campus parking with charging points for electric vehicles
  • Fantastic range of sports facilities and preferential membership packages available
This advertiser has chosen not to accept applicants from your region.
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Research Associate - Inorganic Chemistry

Staffordshire, West Midlands SRG

Posted 1 day ago

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Job Description

permanent

Research Chemist required, based in Staffordshire. Degree in Chemistry is essential, no industrial experience necessary but is advantageous.

Research Chemist - Inorganic Chemistry

Staffordshire (commutable from Stoke, Stafford, Crewe and surrounding areas)

Salary - 26,000 - 32,000 (depending on experience)

Permanent

SRG is working with a leading researcher and manufacturer, who develop and manufacture high performance speciality chemicals. Based in the Staffordshire area, they have recently started hiring for a new member of their R&D team. This is a great opportunity for a chemistry graduate or PhD chemist with a strong research background in polymers, materials or inorganic synthesis to make their first move in the industry. You will join a company that is quickly growing and adding new state-of-the-art equipment to their lab. Applications from graduates are welcome and individuals with previous industry experience would be considered at the upper end of the salary scale.

Benefits: Flexible working hours (34.5 + hour lunch break). 25 days holiday + bank holidays. Company bonus and pension schemes

Role Description

  • Synthesising novel materials for applications within the polymers and coatings industries.
  • Scaling up chemical production processes to pilot plant scale.
  • Liaising with customers, consulting and providing detailed technical knowledge and demonstrations.
  • Solving a diverse set of problems relating to new product development
  • General laboratory housekeeping and working with technical reports and safety data sheets

Requirements

  • Degree in Chemistry with a focus on a synthesis project (inorganic, organic, materials chemistry)
  • Proven ability to do research and think independently. A PhD or relevant industry experience would be a distinct advantage.
  • Recent experience working in an academic or industrial laboratory
  • Ability to travel or relocate to the Staffordshire area.
  • Any past experience within polymer formulation or materials development would be an advantage.
  • Full right to work in the UK.

If you would like to apply for this position, please use the link provided. Alternatively, please email a copy of your CV to For more information regarding this position or any others, please call Will on (phone number removed). If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit (url removed) to view our other vacancies.

SRG is the UK's number one recruitment company specialising in the scientific, engineering, clinical, pharmaceutical, food/FMCG, energy & renewables, biotech, chemical and medical device sectors. As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

Keywords: graduate chemist, PhD, polymers, materials, R&D, product development, laboratory, chemist, chemistry, NPD, graduate, synthesis, inorganic, research

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

This advertiser has chosen not to accept applicants from your region.

Research Associate - Inorganic Chemistry

ST1 Stoke on Trent, West Midlands SRG

Posted 1 day ago

Job Viewed

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Job Description

full time

Research Chemist required, based in Staffordshire. Degree in Chemistry is essential, no industrial experience necessary but is advantageous.

Research Chemist - Inorganic Chemistry

Staffordshire (commutable from Stoke, Stafford, Crewe and surrounding areas)

Salary - 26,000 - 32,000 (depending on experience)

Permanent

SRG is working with a leading researcher and manufacturer, who develop and manufacture high performance speciality chemicals. Based in the Staffordshire area, they have recently started hiring for a new member of their R&D team. This is a great opportunity for a chemistry graduate or PhD chemist with a strong research background in polymers, materials or inorganic synthesis to make their first move in the industry. You will join a company that is quickly growing and adding new state-of-the-art equipment to their lab. Applications from graduates are welcome and individuals with previous industry experience would be considered at the upper end of the salary scale.

Benefits: Flexible working hours (34.5 + hour lunch break). 25 days holiday + bank holidays. Company bonus and pension schemes

Role Description

  • Synthesising novel materials for applications within the polymers and coatings industries.
  • Scaling up chemical production processes to pilot plant scale.
  • Liaising with customers, consulting and providing detailed technical knowledge and demonstrations.
  • Solving a diverse set of problems relating to new product development
  • General laboratory housekeeping and working with technical reports and safety data sheets

Requirements

  • Degree in Chemistry with a focus on a synthesis project (inorganic, organic, materials chemistry)
  • Proven ability to do research and think independently. A PhD or relevant industry experience would be a distinct advantage.
  • Recent experience working in an academic or industrial laboratory
  • Ability to travel or relocate to the Staffordshire area.
  • Any past experience within polymer formulation or materials development would be an advantage.
  • Full right to work in the UK.

If you would like to apply for this position, please use the link provided. Alternatively, please email a copy of your CV to For more information regarding this position or any others, please call Will on (phone number removed). If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit (url removed) to view our other vacancies.

SRG is the UK's number one recruitment company specialising in the scientific, engineering, clinical, pharmaceutical, food/FMCG, energy & renewables, biotech, chemical and medical device sectors. As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

Keywords: graduate chemist, PhD, polymers, materials, R&D, product development, laboratory, chemist, chemistry, NPD, graduate, synthesis, inorganic, research

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

This advertiser has chosen not to accept applicants from your region.

Senior Clinical Research Associate

RBW Consulting

Posted today

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Job Description

  • Job Title: Senior CRA / Senior CRA II
  • Location: Remote in UK
  • Salary: £50,000 - £58,000
  • Additional Benefits: Car allowance (or company car) and bonus
  • Company: Global CRO


RBW Consulting is thrilled to present an exciting opportunity on behalf of one of our esteemed clients. As one of the few rapidly growing Contract Research Organizations (CROs) for UK studies, our client is expanding their site management team with multiple hires this year. They are involved in a diverse range of studies, including cutting-edge research in advanced therapies such as CAR-T.


Join a highly experienced team dedicated to excellence in clinical research. We are seeking skilled monitors with a minimum of 3 years of CRA experience. In this role, you will benefit from a supportive management team committed to your professional growth. They provide clear guidance on the skills needed for advancement and offer fluid career development opportunities across various departments.


This company prioritizes quality over metrics and is currently generating significant excitement within their UK team.


Key accountabilities

  • Autonomy of investigator sites with full responsibility for the successful management of sites through study life cycle (start-up to close-out);
  • Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3 and within all available therapeutic areas;
  • Prepare accordingly and attend investigator meetings, coordinating timely delivery and subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues;
  • Perform source document verification and case report form review;
  • Perform regulatory document review;
  • Conduct study drug inventory;
  • Perform adverse event and serious adverse event reporting and follow-up; and
  • Assess patient recruitment and retention.


Qualifications

  • Bachelor of Science in health-related field (or equivalent)
  • Proven CRA experience; 3 years minimum


Why Join?

  • Supportive Environment : Build strong relationships with a transparent management team focused on your development.
  • Innovative Approach : Work with a company that embraces a 360 monitoring approach and leverages AI to enhance efficiency and save time.
  • Results-Driven KPIs : Our client's key performance indicators are centered around tangible study outcomes, such as patient recruitment, visit reports, and resolving site issues.


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.

This advertiser has chosen not to accept applicants from your region.
 

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  42. inventory_2 Logistics & Warehousing
  43. supervisor_account Management
  44. supervisor_account Management Consultancy
  45. supervisor_account Manufacturing & Production
  46. campaign Marketing
  47. build Mechanical Engineering
  48. perm_media Media & PR
  49. local_hospital Medical
  50. local_hospital Military & Public Safety
  51. local_hospital Mining
  52. medical_services Nursing
  53. local_gas_station Oil & Gas
  54. biotech Pharmaceutical
  55. checklist_rtl Project Management
  56. shopping_bag Purchasing
  57. home_work Real Estate
  58. person_search Recruitment Consultancy
  59. store Retail
  60. point_of_sale Sales
  61. science Scientific Research & Development
  62. wifi Telecoms
  63. psychology Therapy
  64. pets Veterinary
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