What Jobs are available for Research And Development in Oxfordshire?
Showing 275 Research And Development jobs in Oxfordshire
Graduate Rotational Programme - Research & Development
OX1 1BU Oxford, South East
£30000 Annually
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Posted 7 days ago
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Job Description
Our client, a world-renowned academic and research institution, is seeking ambitious and bright graduates to join their prestigious Graduate Rotational Programme in Oxford, Oxfordshire, UK . This programme offers a unique opportunity for recent graduates to gain exposure to a variety of cutting-edge research and development projects, fostering their career growth within a leading scientific environment. Over a 18-month period, participants will rotate through different departments, contributing to diverse projects in areas such as biotechnology, materials science, computational modelling, and experimental physics. Each rotation will provide hands-on experience, mentorship from senior researchers, and opportunities to develop advanced technical skills. The programme is designed to identify and nurture future leaders in scientific innovation. Participants will be involved in data collection, analysis, experimental design, literature reviews, and contributing to the writing of research papers and reports. Collaboration with research teams, adherence to laboratory safety protocols, and effective communication of findings are essential. This role offers a hybrid work model, blending essential in-lab or office-based work with remote access to data and resources, promoting a balanced and productive working experience. The ideal candidate will possess a strong academic background in a relevant STEM field, a curious and inquisitive mind, and a genuine passion for scientific discovery. Excellent analytical skills, strong problem-solving abilities, and a proactive approach to learning are paramount. Graduates will gain invaluable experience, build a robust professional network, and lay the foundation for a successful career in research and development. This is an exceptional chance to contribute to groundbreaking scientific endeavours and develop essential professional competencies.
Programme Structure:
Programme Structure:
- 18-month rotational programme across various R&D departments.
- Exposure to diverse scientific disciplines and research methodologies.
- Hands-on experience in experimental design, data analysis, and scientific reporting.
- Mentorship from leading researchers and scientists.
- Opportunities to present findings and contribute to publications.
- Development of technical skills and professional competencies.
- Hybrid work environment to foster collaboration and flexibility.
- Recent graduate with a Bachelor's or Master's degree in a relevant STEM field (e.g., Biology, Chemistry, Physics, Engineering, Computer Science, Mathematics).
- Achieved or predicted to achieve a 2:1 degree classification or higher.
- Demonstrated passion for research and scientific inquiry.
- Strong analytical and problem-solving skills.
- Excellent communication and interpersonal abilities.
- Ability to work effectively both independently and as part of a team.
- Eligibility to work in the UK.
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0
Graduate Trainee - Research and Development
OX1 1BD Oxford, South East
£30000 Annually
WhatJobs
Posted 18 days ago
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Job Description
Our client is seeking bright and enthusiastic Graduate Trainees to join their esteemed Research and Development department. This is an exceptional opportunity for individuals with a strong academic background and a passion for innovation to gain invaluable practical experience in a leading research environment. You will be involved in various stages of the R&D lifecycle, contributing to groundbreaking projects under the guidance of experienced scientists and engineers.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Assist senior researchers and engineers in conducting experiments and gathering data.
- Perform literature reviews and synthesize information on relevant scientific and technological advancements.
- Contribute to the design and execution of research projects.
- Analyze experimental data using statistical and analytical tools.
- Prepare technical reports, presentations, and documentation of research findings.
- Operate and maintain laboratory equipment and ensure adherence to safety protocols.
- Collaborate with team members to troubleshoot technical challenges and propose solutions.
- Stay updated on industry trends and emerging technologies within the R&D field.
- Participate in team meetings and contribute to project planning and discussions.
- Support the development and testing of prototypes or new product features.
- Ensure meticulous record-keeping of all research activities and results.
- Adhere to quality control standards and company R&D procedures.
Qualifications:
- A recent graduate with a Bachelor's or Master's degree in a relevant scientific or engineering discipline (e.g., Physics, Chemistry, Biology, Engineering, Computer Science).
- Strong analytical and problem-solving skills.
- Excellent research and information synthesis abilities.
- Proficiency in data analysis and relevant software (e.g., Excel, MATLAB, R, Python).
- Good written and verbal communication skills.
- Ability to work effectively both independently and as part of a team.
- Strong attention to detail and commitment to accuracy.
- A genuine interest in research and development and a desire to learn.
- Familiarity with laboratory practices and safety procedures is a plus.
- Proximity to Oxford, Oxfordshire, UK is required for this role.
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1
Senior Research Scientist - Pharmaceutical Development
OX1 3QG Oxford, South East
£60000 Annually
WhatJobs
Posted 17 days ago
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Job Description
Our client, a pioneering biopharmaceutical company dedicated to advancing human health, is seeking a highly skilled and innovative Senior Research Scientist to join their world-class, fully remote R&D team. This role is crucial for driving forward cutting-edge drug discovery and development programs. The ideal candidate will possess a deep understanding of pharmaceutical sciences and a proven track record in experimental design, data analysis, and project leadership. This remote position offers an unparalleled opportunity to contribute to life-changing therapies from a location of your choice.
Key Responsibilities:
Key Responsibilities:
- Design, execute, and interpret complex experiments related to drug discovery and development, focusing on target validation, lead optimization, and preclinical studies.
- Develop and implement novel assays and methodologies to assess drug efficacy, safety, and pharmacokinetic profiles.
- Analyze and critically evaluate experimental data, generating comprehensive reports and presenting findings to internal teams and external collaborators.
- Lead research projects, providing scientific direction, mentoring junior scientists, and managing timelines and resources effectively within a remote setting.
- Collaborate closely with cross-functional teams, including medicinal chemistry, biology, pharmacology, and regulatory affairs, to advance projects through the pipeline.
- Stay abreast of the latest scientific literature, technological advancements, and industry trends in pharmaceutical research.
- Contribute to the preparation of scientific publications, patents, and regulatory submissions.
- Ensure strict adherence to laboratory safety standards and good experimental practices.
- Actively participate in team meetings and scientific discussions, contributing valuable insights and fostering a collaborative research environment.
- Ph.D. in Pharmacology, Biochemistry, Molecular Biology, or a related life science discipline.
- Minimum of 5 years of post-doctoral or industry experience in pharmaceutical research and development.
- Demonstrated expertise in one or more therapeutic areas and associated research methodologies.
- Strong track record of successful experimental design, execution, and data interpretation.
- Excellent understanding of drug discovery processes and regulatory requirements.
- Proven ability to lead projects and mentor scientific staff.
- Exceptional written and verbal communication skills, with the ability to present complex scientific information clearly and concisely.
- Proficiency in relevant scientific software and data analysis tools.
- Ability to work independently, manage priorities effectively, and thrive in a remote, collaborative environment.
- Experience with in vivo models and preclinical development is highly desirable.
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2
Principal Clinical Research Associate
OX1 3PW Oxford, South East
£60000 Annually
WhatJobs
Posted 3 days ago
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Job Description
Our client is a renowned pharmaceutical research organization based in the vibrant scientific hub of Oxford, Oxfordshire, UK . They are seeking a highly experienced and diligent Principal Clinical Research Associate (CRA) to join their dedicated clinical operations team. This hybrid role offers a balanced approach to work, combining remote flexibility with essential in-person collaboration. You will be instrumental in overseeing and managing clinical trials, ensuring adherence to protocols, and upholding the highest standards of data integrity and patient safety.
Key Responsibilities:
Qualifications:
This is an outstanding opportunity to contribute to significant clinical research advancements within a respected organization. Join our team in Oxford and leverage your expertise to drive successful clinical trial outcomes in a supportive hybrid work environment.
Key Responsibilities:
- Initiate, monitor, and close-out clinical trial sites according to Good Clinical Practice (GCP) and relevant regulatory requirements.
- Conduct site visits (pre-study, initiation, interim monitoring, and close-out) to assess patient recruitment, data accuracy, and regulatory compliance.
- Build and maintain strong relationships with investigators, site staff, and study teams.
- Ensure timely collection, review, and query resolution of clinical data, working closely with data management teams.
- Identify and report adverse events and deviations from protocols, implementing corrective and preventative actions as needed.
- Train and mentor junior CRAs and site personnel on study procedures and regulatory expectations.
- Prepare comprehensive site monitoring reports and contribute to the overall study progress reports.
- Manage site budgets and vendor interactions where applicable.
- Act as a key point of contact for assigned clinical trial sites, providing support and guidance throughout the study lifecycle.
- Contribute to the development and review of clinical trial protocols, case report forms (CRFs), and other essential study documents.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field. A Master's degree or equivalent is preferred.
- Minimum of 7 years of progressive experience as a Clinical Research Associate within the pharmaceutical or biotechnology industry.
- In-depth knowledge of ICH-GCP guidelines, FDA regulations, and other applicable regulatory requirements.
- Proven ability to independently manage multiple clinical trial sites and complex studies.
- Excellent communication, interpersonal, and organizational skills.
- Strong critical thinking and problem-solving abilities.
- Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to travel to clinical sites as required (approximately 40-50%).
- Demonstrated leadership potential and experience in mentoring junior staff.
This is an outstanding opportunity to contribute to significant clinical research advancements within a respected organization. Join our team in Oxford and leverage your expertise to drive successful clinical trial outcomes in a supportive hybrid work environment.
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3
Senior Clinical Research Associate
OX1 4BH Oxford, South East
£50000 Annually
WhatJobs
Posted 13 days ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a highly experienced Senior Clinical Research Associate (CRA) to contribute to their innovative drug development programs. This hybrid role offers a blend of remote work for administrative tasks and essential on-site visits to clinical trial sites. You will be responsible for monitoring and managing clinical trials to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. Key duties include site selection and initiation, regular site visits for data monitoring and source document verification, training site staff, and ensuring timely and accurate data collection. The ideal candidate will have a strong background in clinical research, with extensive experience in monitoring trials across various therapeutic areas. Excellent knowledge of regulatory affairs and ICH-GCP is mandatory. You will play a crucial role in ensuring the integrity and quality of trial data, as well as maintaining positive relationships with investigators and site staff. Strong analytical and problem-solving skills are essential for identifying and resolving potential issues. The ability to work independently, manage your time effectively, and travel as needed is critical. We are looking for a dedicated and meticulous professional committed to advancing pharmaceutical research. If you are a seasoned CRA looking for a challenging and rewarding opportunity within a dynamic pharmaceutical environment, and you are based in or near Oxford, Oxfordshire, UK , we invite you to apply.
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4
Clinical Research Associate (Remote)
OX1 2JD Oxford, South East
£45000 Annually
WhatJobs
Posted 14 days ago
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Job Description
Our client, a pioneering force in medical research and healthcare solutions, is actively seeking a dedicated Clinical Research Associate to join their fully remote team. This position is crucial for advancing groundbreaking studies and ensuring the integrity of clinical trials. As a remote Clinical Research Associate, you will play a vital role in monitoring study conduct, ensuring compliance with protocols, and managing data integrity from the comfort of your home office. This role demands exceptional organizational skills, a meticulous approach to detail, and a profound understanding of clinical research principles.
Key Responsibilities:
Essential Qualifications and Experience:
Key Responsibilities:
- Conduct site visits (remote or on-site as required, though the role is remote-first) to assess protocol compliance, data accuracy, and patient safety.
- Ensure that clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP) guidelines.
- Manage and monitor clinical trial sites remotely, including source data verification, query resolution, and essential document review.
- Communicate effectively with investigators, site staff, and internal project teams to address issues and ensure study progress.
- Oversee the accurate and timely entry of data into clinical databases.
- Prepare and present monitoring reports and escalate any site-specific issues or trends.
- Ensure the proper handling and accountability of investigational product.
- Contribute to the development of study-related documents, such as protocols and case report forms.
- Maintain a strong understanding of therapeutic areas and disease processes relevant to assigned trials.
Essential Qualifications and Experience:
- Bachelor's degree in a life science, nursing, or related field. Advanced degree preferred.
- Minimum of 3 years of direct experience as a Clinical Research Associate, with a strong understanding of GCP, ICH guidelines, and regulatory requirements.
- Demonstrated experience in remote monitoring and virtual site management.
- Proficiency in using Electronic Data Capture (EDC) systems and Clinical Trial Management Systems (CTMS).
- Excellent written and verbal communication skills, with the ability to build rapport and trust with site personnel remotely.
- Strong analytical and problem-solving skills, with meticulous attention to detail.
- Ability to work independently, manage time effectively, and prioritize tasks in a remote work environment.
- Must have a reliable internet connection and a suitable home office setup.
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5
Senior Clinical Research Associate (CRA)
OX2 8BN Oxford, South East
£55000 Annually
WhatJobs
Posted 6 days ago
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Job Description
Our client, a leading global pharmaceutical research organisation, is seeking an experienced Senior Clinical Research Associate (CRA) to join their innovative team. This exciting role is based at their state-of-the-art facility in **Oxford, Oxfordshire, UK**, a hub for cutting-edge biomedical research. As a Senior CRA, you will play a critical role in the planning, execution, and monitoring of clinical trials, ensuring compliance with all regulatory requirements and study protocols. You will be responsible for site selection, initiation, monitoring, and close-out activities, as well as data verification and query resolution. The ideal candidate will possess extensive knowledge of Good Clinical Practice (GCP), relevant regulatory guidelines (e.g., ICH), and a proven ability to manage multiple clinical trial sites effectively. Your primary focus will be on ensuring the safety of study participants and the integrity of the data collected.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Manage assigned clinical trial sites to ensure adherence to protocol, GCP, and regulatory requirements.
- Conduct site visits, including pre-study, initiation, interim monitoring, and close-out visits.
- Verify the accuracy, completeness, and integrity of clinical data through source document verification.
- Identify, report, and resolve protocol deviations and safety concerns in a timely manner.
- Ensure all regulatory documentation is complete, accurate, and maintained according to study requirements.
- Liaise with investigators, site staff, and internal project teams to facilitate trial progress.
- Train and mentor junior CRAs and new study site personnel.
- Contribute to the development of study-related documents, such as protocols, case report forms (CRFs), and monitoring plans.
- Ensure timely reporting of study progress and site performance to project management.
- Maintain up-to-date knowledge of therapeutic areas, company policies, and regulatory changes.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 5 years of experience as a Clinical Research Associate, with demonstrated experience in a senior capacity.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements.
- Experience in managing multiple complex clinical trials across various therapeutic areas.
- Excellent communication, interpersonal, and organisational skills.
- Strong problem-solving abilities and attention to detail.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Willingness to travel as required.
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6
Clinical Research Associate (CRA) - Oncology
OX1 3PA Oxford, South East
£45000 Annually
WhatJobs
Posted 16 days ago
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Job Description
Our client, a globally recognised pharmaceutical company with a significant presence in Oxford, Oxfordshire, UK , is seeking a skilled and motivated Clinical Research Associate (CRA) to join their innovative oncology research team. This role is critical in ensuring the successful execution of clinical trials, adhering to strict regulatory guidelines and ethical standards. You will be responsible for site selection, initiation, monitoring, and closure activities for clinical studies within the oncology therapeutic area. This involves building strong relationships with investigators and site staff, ensuring data accuracy and integrity, and overseeing patient safety throughout the trial duration. The successful candidate will possess excellent communication and interpersonal skills, a keen eye for detail, and a solid understanding of Good Clinical Practice (GCP) and relevant regulatory requirements. You will conduct routine monitoring visits to clinical sites, assess protocol compliance, and manage essential trial documentation. Travel to clinical sites across the UK will be a requirement of this role. We are looking for individuals with a background in life sciences, nursing, or a related field, coupled with direct experience as a CRA or in a similar clinical research role. Expertise in oncology drug development is highly desirable. This position offers a unique opportunity to contribute to cutting-edge research aimed at improving cancer patient outcomes. You will work within a supportive and collaborative environment, with opportunities for professional development and career advancement. The hybrid nature of this role allows for flexibility while maintaining essential on-site collaboration and site visits.
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7
Senior Clinical Research Associate (Oncology)
OX1 3PA Oxford, South East
£55000 Annually
WhatJobs
Posted 18 days ago
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Job Description
A prestigious pharmaceutical company with significant operations in **Oxford, Oxfordshire**, is looking for an experienced Senior Clinical Research Associate (CRA) specializing in Oncology. This is an office-based role, offering a unique chance to contribute to groundbreaking drug development in a collaborative research environment. You will be responsible for the full lifecycle management of clinical trials, ensuring adherence to Good Clinical Practice (GCP), regulatory requirements, and study protocols. Your duties will encompass site initiation, monitoring, and close-out visits, verifying the accuracy and completeness of clinical data, and managing investigational product accountability. You will serve as the primary point of contact for study sites, building strong relationships with investigators and site staff, and addressing any queries or issues that arise. This role requires meticulous attention to detail, exceptional organisational skills, and the ability to interpret complex scientific and medical information. You will actively participate in study team meetings, contribute to the development of study-related documents, and ensure timely data capture and query resolution. The ideal candidate will hold a Bachelor's degree in a life science, nursing, or related field, with a minimum of 5 years of progressive experience as a Clinical Research Associate, with a substantial focus on oncology trials. A thorough understanding of oncology indications, treatment regimens, and related laboratory assessments is critical. Proven experience in performing site monitoring visits, including source data verification and regulatory compliance checks, is essential. Strong knowledge of ICH-GCP guidelines and applicable regulatory requirements (e.g., FDA, EMA) is mandatory. Excellent interpersonal and communication skills, both written and verbal, are required to effectively interact with a diverse range of stakeholders. The ability to manage multiple priorities and meet tight deadlines in a fast-paced environment is crucial. This is an excellent career opportunity for a dedicated CRA to deepen their expertise in oncology research and make a tangible contribution to advancing patient care.
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8
Senior Clinical Research Associate (CRA)
OX1 1AA Oxford, South East
£55000 annum + ben
WhatJobs
Posted 20 days ago
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Job Description
Our client, a renowned pharmaceutical company, is seeking a highly experienced Senior Clinical Research Associate (CRA) to join their dedicated clinical operations team based in Oxford, Oxfordshire, UK . This is an office-based position requiring significant on-site presence and travel.
As a Senior CRA, you will play a crucial role in ensuring the quality, integrity, and timely completion of clinical trials. You will be responsible for monitoring study sites, verifying data accuracy, ensuring compliance with protocols and regulations, and maintaining strong relationships with investigators and site staff.
Key Responsibilities:
As a Senior CRA, you will play a crucial role in ensuring the quality, integrity, and timely completion of clinical trials. You will be responsible for monitoring study sites, verifying data accuracy, ensuring compliance with protocols and regulations, and maintaining strong relationships with investigators and site staff.
Key Responsibilities:
- Conduct pre-study, initiation, interim, and close-out monitoring visits for clinical trial sites in accordance with the Clinical Monitoring Plan.
- Ensure compliance with Good Clinical Practice (GCP), protocol, regulatory requirements, and company SOPs.
- Verify the accuracy, completeness, and validity of study data through source data verification (SDV) and review of case report forms (CRFs).
- Manage assigned clinical trial sites, ensuring adherence to study timelines and budgets.
- Build and maintain strong, collaborative relationships with investigators, site staff, and other stakeholders.
- Identify, document, and track site issues, deviations, and adverse events; implement corrective and preventative actions (CAPAs).
- Prepare and present monitoring visit reports to the study team and management in a timely manner.
- Ensure investigational product is administered and accounted for correctly according to the protocol.
- Participate in investigator meetings and training sessions.
- Contribute to the development and finalization of essential study documents, including protocols, ICFs, and CRFs.
- Mentor and provide guidance to junior CRAs as needed.
- Act as a primary point of contact for assigned sites and support them throughout the trial lifecycle.
- Ensure timely resolution of site-related queries and issues.
- 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, with a proven track record of successful site monitoring.
- In-depth knowledge of GCP, ICH guidelines, and relevant regulatory requirements.
- Demonstrated experience in SDV and query resolution.
- Excellent understanding of clinical trial processes and documentation.
- Strong therapeutic area knowledge is a plus.
- Exceptional organizational, time management, and problem-solving skills.
- Outstanding written and verbal communication and interpersonal skills.
- Ability to travel extensively (up to 60%) to various clinical trial sites.
- Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to work independently and as part of a cross-functional team.
- Detail-oriented with a high level of accuracy.
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