What Jobs are available for Research And Development in Bristol?
Showing 250 Research And Development jobs in Bristol
Remote AI/ML Engineer, Research & Development
BS1 1AA Bristol, South West
£70000 Annually
WhatJobs
Posted 18 days ago
Job Viewed
Job Description
Our client is seeking a brilliant and innovative Remote AI/ML Engineer to join their cutting-edge Research & Development team. This fully remote position offers an exceptional opportunity to work on the forefront of AI and emerging technologies from anywhere in the world, contributing to groundbreaking projects that will shape the future. You will be instrumental in designing, developing, and deploying sophisticated machine learning models and AI systems that solve complex real-world problems. This role demands a strong theoretical foundation in AI/ML principles, practical experience with relevant programming languages and frameworks, and a creative approach to algorithm development and data analysis. Key responsibilities include researching new AI/ML techniques, building and training predictive models, evaluating model performance, and integrating solutions into existing platforms. You will collaborate closely with a globally distributed team of engineers, researchers, and product managers, leveraging remote collaboration tools to drive innovation. Our client values a proactive, experimental mindset and encourages exploration of novel approaches. The ideal candidate will possess a deep understanding of deep learning, natural language processing, computer vision, or other AI sub-fields, along with robust software engineering skills. You will be responsible for data preprocessing, feature engineering, model optimization, and ensuring the scalability and efficiency of AI solutions. This is a chance to work on challenging problems with significant impact, contributing to advancements in AI that will redefine industries. We are looking for individuals who are passionate about pushing the boundaries of artificial intelligence and eager to contribute to a dynamic, forward-thinking, and fully remote organization.
Key Responsibilities:
Key Responsibilities:
- Design, develop, and implement advanced AI and Machine Learning models.
- Conduct research into novel AI/ML algorithms and techniques.
- Process, clean, and analyze large datasets for model training.
- Build, train, and evaluate machine learning models for various applications.
- Optimize model performance for accuracy, efficiency, and scalability.
- Collaborate with a distributed team of engineers and researchers on AI projects.
- Deploy and integrate AI solutions into production environments.
- Stay current with the latest advancements in AI and machine learning research.
- Document and present research findings and project progress.
- Master's or Ph.D. in Computer Science, Artificial Intelligence, Machine Learning, or a related quantitative field.
- Proven experience in developing and deploying AI/ML models.
- Proficiency in programming languages such as Python, Java, or C++.
- Experience with ML frameworks (e.g., TensorFlow, PyTorch, Scikit-learn).
- Strong understanding of statistical modeling, data mining, and algorithms.
- Experience with cloud platforms (AWS, Azure, GCP) and big data technologies is a plus.
- Excellent problem-solving, analytical, and critical thinking skills.
- Strong communication and collaboration abilities, especially in a remote team setting.
Is this job a match or a miss?
This advertiser has chosen not to accept applicants from your region.
0
Senior Clinical Research Associate
BS34 5TT Bristol, South West
£50000 Annually
WhatJobs
Posted 21 days ago
Job Viewed
Job Description
Our client, a leading Contract Research Organization (CRO) committed to accelerating the development of life-saving medicines, is looking for a highly experienced Senior Clinical Research Associate (CRA) to join their esteemed team in **Bristol, South West England, UK**. This role offers an excellent opportunity to contribute to diverse clinical trials across various therapeutic areas. You will be responsible for the full lifecycle of clinical trial site management, ensuring compliance with Good Clinical Practice (GCP), regulatory requirements, and study protocols. Key responsibilities include site selection and initiation, monitoring site performance, ensuring accurate and timely data collection, and resolving site issues. You will build strong relationships with investigators and site staff, providing essential training and support to ensure the smooth running of clinical studies. Your role will involve conducting on-site and remote monitoring visits, maintaining comprehensive study documentation, and managing study timelines and budgets effectively. The ideal candidate will have a Bachelor's degree in a life science or healthcare-related field, with a minimum of 4-5 years of experience as a Clinical Research Associate. A thorough understanding of ICH-GCP guidelines and regulatory requirements is essential. Proven experience in site monitoring, data management, and a strong understanding of clinical trial processes are required. Excellent communication, organizational, and problem-solving skills are paramount. The ability to work independently, manage multiple priorities, and travel to sites as needed is crucial. This hybrid role allows for a flexible working arrangement, combining essential on-site activities with the convenience of remote work, promoting a healthy work-life integration. The successful applicant will be a meticulous and dedicated professional, passionate about contributing to the advancement of clinical research and patient well-being.
Is this job a match or a miss?
This advertiser has chosen not to accept applicants from your region.
1
Senior Clinical Research Associate
BS1 4 Bristol, South West
£50000 Annually
WhatJobs
Posted 22 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical research organisation, is seeking a highly motivated and experienced Senior Clinical Research Associate (CRA) to join their team based in Bristol, South West England, UK . This role is essential for the successful execution and monitoring of clinical trials, ensuring compliance with regulatory standards and protocols.
Responsibilities:
Responsibilities:
- Conduct site visits (initiation, monitoring, close-out) to assess protocol adherence, data accuracy, and patient safety.
- Ensure all clinical trial activities are conducted in accordance with Good Clinical Practice (GCP), ICH guidelines, and applicable regulations.
- Verify source data and documentation for accuracy and completeness against case report forms (CRFs).
- Manage communication between investigational sites and the clinical trial team, addressing any site-related issues promptly.
- Train site personnel on trial procedures, protocols, and regulatory requirements.
- Monitor recruitment progress and protocol compliance at assigned sites.
- Prepare and submit accurate site visit reports and follow-up on action items.
- Maintain effective working relationships with investigators, site staff, and study sponsors.
- Identify and escalate potential risks and issues to the Clinical Trial Manager.
- Ensure timely collection and review of essential trial documents.
- Contribute to the development and review of study-related documents, such as protocols and CRFs.
- Assist in the selection and evaluation of potential investigational sites.
- Uphold the highest standards of data integrity and patient confidentiality.
- A Bachelor's degree in a life science, nursing, pharmacy, or related discipline. Advanced degree preferred.
- Minimum of 3-5 years of independent clinical monitoring experience.
- Thorough understanding of GCP, ICH guidelines, and regulatory requirements for clinical trials.
- Proven experience in therapeutic areas such as oncology, cardiology, or neurology.
- Excellent communication, interpersonal, and organisational skills.
- Ability to travel extensively (up to 60%) to investigational sites across the region and potentially internationally.
- Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Strong problem-solving abilities and a proactive approach to managing trial activities.
- Ability to work independently and manage time effectively.
- Detail-oriented with a commitment to accuracy and quality.
Is this job a match or a miss?
This advertiser has chosen not to accept applicants from your region.
2
Senior Clinical Research Associate (Remote)
BS1 3JS Bristol, South West
£55000 Annually
WhatJobs
Posted 4 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is looking for an experienced Senior Clinical Research Associate (CRA) to join their fully remote global clinical operations team. This pivotal role requires a seasoned professional to oversee and manage clinical trial activities, ensuring adherence to regulatory standards and protocols from a remote location. You will be responsible for site selection, initiation, monitoring, and close-out visits, performing these duties through a combination of virtual interactions and necessary on-site travel. The ideal candidate will possess a strong background in clinical research, with a deep understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements (e.g., FDA, EMA). A minimum of 3-5 years of experience as a CRA is essential, with demonstrated success in managing multiple complex clinical trials simultaneously. You will be tasked with ensuring data integrity, patient safety, and the overall quality of clinical trial execution. Excellent communication, negotiation, and interpersonal skills are paramount, as you will liaise with investigators, site staff, and internal project teams. Proficiency in electronic data capture (EDC) systems, clinical trial management systems (CTMS), and other relevant software is required. This role demands exceptional organizational skills, meticulous attention to detail, and the ability to work independently and proactively in a remote setting. You will contribute to the development of study protocols, Case Report Forms (CRFs), and other essential trial documents. The successful candidate will be adept at problem-solving, risk assessment, and implementing corrective and preventive actions (CAPAs) to maintain trial timelines and objectives. This is an outstanding opportunity to contribute to the development of life-changing medicines and advance your career in a dynamic and supportive remote environment within the pharmaceutical industry, impacting global health initiatives related to **Bristol, South West England, UK**.
Is this job a match or a miss?
This advertiser has chosen not to accept applicants from your region.
3
Senior Clinical Research Associate (CRA)
BS1 3AD Bristol, South West
£55000 Annually
WhatJobs
Posted 4 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking an experienced Senior Clinical Research Associate (CRA) to join their team based in Bristol, South West England, UK . This role is integral to the successful execution of clinical trials, ensuring compliance with regulatory standards and maintaining the integrity of trial data. The Senior CRA will be responsible for site monitoring, data verification, and ensuring patient safety throughout the trial process. This hybrid role allows for a blend of remote work and on-site visits to investigational sites.
Responsibilities:
Responsibilities:
- Conduct site initiation, interim monitoring, and close-out visits for clinical trials.
- Ensure adherence to Good Clinical Practice (GCP) guidelines, regulatory requirements, and study protocols.
- Verify the accuracy, completeness, and consistency of clinical trial data through source data verification.
- Monitor patient safety and report adverse events according to established procedures.
- Train and support site personnel on study conduct and regulatory compliance.
- Manage investigational product accountability and ensure proper storage and handling.
- Maintain effective communication with investigators, site staff, and internal project teams.
- Prepare monitoring visit reports and follow up on action items.
- Contribute to the development of study-related documents, such as protocols and case report forms (CRFs).
- Identify and resolve site-level issues and risks in a timely manner.
- Ensure timely submission of trial documentation and data.
- Stay current with industry trends and regulatory updates affecting clinical research.
- Mentor junior CRAs and provide guidance on best practices.
- Bachelor's degree in a life science, nursing, or related field; advanced degree preferred.
- Minimum of 5 years of experience as a Clinical Research Associate in the pharmaceutical or biotechnology industry.
- In-depth knowledge of GCP, ICH guidelines, and relevant regulatory requirements.
- Proven experience in site monitoring and data verification.
- Excellent understanding of clinical trial processes and documentation.
- Strong organizational and time-management skills.
- Exceptional attention to detail and accuracy.
- Effective communication, interpersonal, and problem-solving skills.
- Ability to travel to investigational sites as required.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Relevant certifications (e.g., ACRP, SoCRA) are highly desirable.
- Ability to work independently and as part of a remote team.
Is this job a match or a miss?
This advertiser has chosen not to accept applicants from your region.
4
Clinical Research Associate (CRA) - Oncology
BS1 4AA Bristol, South West
£50000 Annually
WhatJobs
Posted 22 days ago
Job Viewed
Job Description
Our client, a leading global pharmaceutical company, is seeking a dedicated and experienced Clinical Research Associate (CRA) specializing in Oncology to join their innovative team in Bristol, South West England, UK . This critical role involves overseeing and managing all aspects of clinical trials, ensuring compliance with protocols, Good Clinical Practice (GCP), and regulatory requirements. You will be responsible for site selection, initiation, monitoring, and close-out visits, as well as ensuring the quality and integrity of data collected. The ideal candidate will possess a strong understanding of oncology drug development, clinical trial processes, and regulatory guidelines. A proven track record as a CRA, with experience in conducting site audits and resolving issues, is essential. You will liaise effectively with investigators, site staff, and internal project teams to ensure smooth trial progression and timely reporting of adverse events. This hybrid role requires a significant amount of travel to clinical sites within the assigned territory, while also allowing for remote work and flexible scheduling. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is a must. We are looking for a highly organized, detail-oriented professional with excellent communication and interpersonal skills. The ability to work independently, manage multiple priorities, and maintain a high level of professionalism is paramount. If you are passionate about advancing cancer treatments and have a commitment to scientific excellence, we encourage you to apply and contribute to groundbreaking research in Bristol, South West England, UK .
Is this job a match or a miss?
This advertiser has chosen not to accept applicants from your region.
5
Senior Clinical Research Associate (CRA)
BS1 6EH Bristol, South West
£55000 Annually
WhatJobs
Posted 24 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking a highly experienced Senior Clinical Research Associate (CRA) to join their team in Bristol, South West England, UK . This role operates on a hybrid model, offering a blend of remote work and on-site activities. You will be responsible for the planning, execution, and monitoring of clinical trials to ensure compliance with protocols, regulations, and ethical standards. The ideal candidate possesses a strong understanding of drug development processes and has a proven ability to manage complex clinical trial sites.
Key Responsibilities:
Key Responsibilities:
- Initiate, monitor, and close-out clinical trial sites according to protocol and GCP guidelines.
- Conduct site visits (initiation, monitoring, and close-out) to assess compliance and data integrity.
- Ensure accurate and timely collection of clinical data, and manage source document verification.
- Build and maintain strong relationships with investigators, site staff, and study sponsors.
- Oversee subject recruitment and retention strategies at trial sites.
- Identify and report adverse events and protocol deviations.
- Prepare and present study progress reports to internal stakeholders.
- Ensure all regulatory requirements and ethical considerations are met.
- Manage study supplies and investigational product accountability.
- Mentor and support junior CRAs and study team members.
- Bachelor's degree in a life science, nursing, or a related scientific field. Advanced degree is a plus.
- Minimum of 4-5 years of experience as a Clinical Research Associate.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
- Proven experience in site management and monitoring.
- Excellent understanding of medical terminology and clinical trial processes.
- Strong organizational, time management, and problem-solving skills.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Excellent written and verbal communication skills.
- Ability to travel as required to trial sites.
Is this job a match or a miss?
This advertiser has chosen not to accept applicants from your region.
Be The First To Know
About the latest Research and development Jobs in Bristol !
6
Senior Pharmaceutical Research Scientist - Process Development
BS1 4UB Bristol, South West
£65000 Annually
WhatJobs
Posted 18 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company renowned for its commitment to innovation and patient well-being, is seeking a highly skilled Senior Pharmaceutical Research Scientist to join their Process Development team. This critical, lab-based role is situated in our state-of-the-art facility in **Bristol, South West England**. You will play a key role in the development, optimization, and scale-up of manufacturing processes for novel drug substances. This position requires extensive experience in chemical synthesis, process chemistry, and a deep understanding of pharmaceutical manufacturing principles.
Key Responsibilities:
The ideal candidate will possess a PhD or Master's degree in Organic Chemistry, Chemical Engineering, or a related field, with a proven track record in pharmaceutical process development. You must have strong hands-on experience with synthetic chemistry techniques and process scale-up. Excellent understanding of GMP guidelines and regulatory affairs is essential. Strong analytical and problem-solving skills, coupled with exceptional written and verbal communication abilities, are required. This is a hands-on role requiring significant time spent in the laboratory environment within our **Bristol** facility, working collaboratively with a dedicated team of scientists and engineers.
Qualifications:
Key Responsibilities:
- Lead the development and optimization of synthetic routes for active pharmaceutical ingredients (APIs) and intermediates.
- Design and execute experimental plans to improve process efficiency, yield, purity, and safety.
- Scale-up processes from laboratory bench to pilot plant and commercial manufacturing.
- Develop robust analytical methods for in-process controls and final product release testing.
- Troubleshoot and resolve technical challenges encountered during process development and manufacturing.
- Ensure all development activities comply with Good Manufacturing Practice (GMP) and regulatory requirements (e.g., FDA, EMA).
- Author and review technical reports, development summaries, and regulatory submission documents.
- Collaborate effectively with cross-functional teams, including R&D, manufacturing, quality assurance, and regulatory affairs.
- Manage external contract manufacturing organizations (CMOs) as required.
- Stay abreast of new technologies and scientific advancements in pharmaceutical process development.
- Mentor junior scientists and contribute to a culture of continuous improvement and scientific excellence.
The ideal candidate will possess a PhD or Master's degree in Organic Chemistry, Chemical Engineering, or a related field, with a proven track record in pharmaceutical process development. You must have strong hands-on experience with synthetic chemistry techniques and process scale-up. Excellent understanding of GMP guidelines and regulatory affairs is essential. Strong analytical and problem-solving skills, coupled with exceptional written and verbal communication abilities, are required. This is a hands-on role requiring significant time spent in the laboratory environment within our **Bristol** facility, working collaboratively with a dedicated team of scientists and engineers.
Qualifications:
- PhD or Master's degree in Organic Chemistry, Chemical Engineering, or a related discipline.
- Minimum of 5 years of experience in pharmaceutical process development and scale-up.
- Extensive experience in synthetic organic chemistry and process optimization.
- In-depth knowledge of GMP and regulatory requirements in the pharmaceutical industry.
- Proficiency with analytical techniques (e.g., HPLC, GC, NMR, MS).
- Experience with pilot plant operations and technology transfer is highly desirable.
- Strong problem-solving and troubleshooting skills.
- Excellent communication, interpersonal, and team collaboration skills.
- Proven ability to manage projects and mentor junior staff.
Is this job a match or a miss?
This advertiser has chosen not to accept applicants from your region.
7
Remote Senior Clinical Research Associate (CRA)
BS1 3BX Bristol, South West
£60000 Annually
WhatJobs
Posted 23 days ago
Job Viewed
Job Description
Our client is seeking a highly motivated and experienced Senior Clinical Research Associate (CRA) to join their global clinical operations team on a fully remote basis. This crucial role involves overseeing and managing the conduct of clinical trials across various therapeutic areas, ensuring compliance with regulatory standards and protocols. You will be instrumental in guaranteeing the quality and integrity of trial data, the safety of study participants, and the timely completion of studies, all while working remotely.
Key Responsibilities:
Qualifications:
This is a significant opportunity to drive critical research forward from Bristol, South West England, UK (or any UK location). If you are a seasoned CRA passionate about patient care and research integrity, we encourage you to apply.
Key Responsibilities:
- Conduct site selection, initiation, monitoring, and close-out visits for clinical trial sites in accordance with Good Clinical Practice (GCP) guidelines and company SOPs.
- Ensure accurate and timely collection of source data and Case Report Form (CRF) completion.
- Verify the rights and well-being of study participants are protected.
- Monitor study progress, data quality, and protocol adherence at assigned clinical sites.
- Identify, document, and resolve site-related issues and discrepancies.
- Manage communication between the sponsor, clinical sites, and investigational sites.
- Train and mentor new CRAs and site staff on study protocols and procedures.
- Prepare and present site monitoring reports and participate in teleconferences with clinical trial teams.
- Ensure compliance with all applicable regulatory requirements (e.g., FDA, EMA) and company policies.
- Maintain study essential documents and ensure proper filing and archiving.
- Contribute to the development and review of study-related documents, such as protocols, CRFs, and monitoring plans.
- Manage and track site budget and timelines effectively.
- Travel to sites as required for monitoring and auditing purposes (although the role is remote, occasional site visits may be necessary).
Qualifications:
- Bachelor's degree in a life science, nursing, or a related field. Advanced degree or nursing qualification is a plus.
- Minimum of 5 years of experience as a Clinical Research Associate in the pharmaceutical or biotechnology industry.
- Thorough understanding of GCP, ICH guidelines, and relevant regulatory requirements.
- Proven experience in conducting all phases of clinical trial site monitoring.
- Excellent knowledge of clinical trial processes and documentation.
- Strong organisational, time management, and problem-solving skills.
- Exceptional attention to detail and accuracy in data verification and reporting.
- Excellent interpersonal and communication skills, with the ability to build strong relationships with site personnel and internal teams.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to work independently and manage workload effectively in a remote setting.
- Willingness to travel to sites as needed.
- Experience across multiple therapeutic areas is advantageous.
This is a significant opportunity to drive critical research forward from Bristol, South West England, UK (or any UK location). If you are a seasoned CRA passionate about patient care and research integrity, we encourage you to apply.
Is this job a match or a miss?
This advertiser has chosen not to accept applicants from your region.
8
Process Development Engineer
Bristol, South West
£50000 - £60000 Annually
Zenovo
Posted 2 days ago
Job Viewed
Job Description
Job Title: Process Development Engineer
Location : Bristol (Hybrid - 3 Days On-Site Per Week)
Salary : Up to £60,000 (Depending on Experience)
Role Overview
We are seeking a skilled and proactive Process Development Engineer to lead the development, optimisation and implementation of robust manufacturing and assembly processes.
This role is ideal for someone who thrives on improving process performance, ensuring high quality and consistency, and supporting scalable production systems.
The successful candidate will work cross-functionally across engineering, production, quality and supply chain teams to define and refine manufacturing processes that meet operational goals. You will play a critical role in supporting new product introductions and improving existing production workflows.
Job Responsibilities:
Provide technical and operational leadership for on-site process development related to the production of electronic devices.
Lead the creation, implementation, and ongoing maintenance of comprehensive process documentation, including work instructions, assembly layouts, testing protocols, and standard operating procedures (SOPs).
Ensure adherence to industry regulations and quality standards by managing all documentation associated with the assembly and manufacture of electronic components and devices.
Drive continuous improvement initiatives to enhance manufacturing efficiency, departmental performance, and operational accountability.
Contribute to the rollout of new systems and process enhancements, with a focus on improving product traceability, ensuring accurate documentation, and streamlining declarations of conformity for regulatory compliance.
Experience Required:
Proven experience in a Senior Process or Manufacturing Engineering role.
Strong knowledge of process development, technical documentation, and regulatory compliance.
Experience improving operational effectiveness through structured process improvements.
Strong knowledge of assembly techniques, process optimisation, and quality assurance methods.
Experience creating documentation such as standard operating procedures, work instructions and process flows.
Location : Bristol (Hybrid - 3 Days On-Site Per Week)
Salary : Up to £60,000 (Depending on Experience)
Role Overview
We are seeking a skilled and proactive Process Development Engineer to lead the development, optimisation and implementation of robust manufacturing and assembly processes.
This role is ideal for someone who thrives on improving process performance, ensuring high quality and consistency, and supporting scalable production systems.
The successful candidate will work cross-functionally across engineering, production, quality and supply chain teams to define and refine manufacturing processes that meet operational goals. You will play a critical role in supporting new product introductions and improving existing production workflows.
Job Responsibilities:
Provide technical and operational leadership for on-site process development related to the production of electronic devices.
Lead the creation, implementation, and ongoing maintenance of comprehensive process documentation, including work instructions, assembly layouts, testing protocols, and standard operating procedures (SOPs).
Ensure adherence to industry regulations and quality standards by managing all documentation associated with the assembly and manufacture of electronic components and devices.
Drive continuous improvement initiatives to enhance manufacturing efficiency, departmental performance, and operational accountability.
Contribute to the rollout of new systems and process enhancements, with a focus on improving product traceability, ensuring accurate documentation, and streamlining declarations of conformity for regulatory compliance.
Experience Required:
Proven experience in a Senior Process or Manufacturing Engineering role.
Strong knowledge of process development, technical documentation, and regulatory compliance.
Experience improving operational effectiveness through structured process improvements.
Strong knowledge of assembly techniques, process optimisation, and quality assurance methods.
Experience creating documentation such as standard operating procedures, work instructions and process flows.
Is this job a match or a miss?
This advertiser has chosen not to accept applicants from your region.
9