411 Researchers jobs in Oxford
Senior Scientific Research Scientist - Remote
RG1 2NN Reading, South East
£55000 Annually
WhatJobs
Posted 2 days ago
Job Viewed
Job Description
Our client is seeking an accomplished Senior Scientific Research Scientist to join their innovative R&D department. This hybrid role offers the flexibility to work both remotely and from their state-of-the-art facility located in **Reading, Berkshire, UK**. You will be instrumental in driving forward groundbreaking research initiatives, contributing to the design and execution of experimental protocols, and analyzing complex data sets to generate actionable insights. The ideal candidate possesses a Ph.D. in a relevant scientific discipline, a strong publication record, and a passion for scientific discovery. You will collaborate closely with a multidisciplinary team of scientists and engineers, both in person and virtually, to translate theoretical concepts into tangible advancements.
Responsibilities:
Responsibilities:
- Design, conduct, and interpret complex scientific experiments and research projects within your area of expertise.
- Develop and refine experimental methodologies, ensuring scientific rigor and reproducibility.
- Analyze large and complex datasets using advanced statistical and computational techniques.
- Collaborate with cross-functional teams, including chemists, biologists, physicists, and engineers, to achieve research objectives.
- Prepare and present research findings through written reports, scientific publications, and oral presentations to internal and external stakeholders.
- Contribute to the strategic planning and direction of research programs.
- Maintain detailed and accurate laboratory notebooks and research records.
- Stay abreast of the latest scientific literature, technological advancements, and emerging trends in relevant fields.
- Mentor junior researchers and provide technical guidance and support.
- Ensure compliance with all laboratory safety protocols and ethical guidelines.
- Contribute to patent applications and intellectual property development.
- Assist in the procurement and management of laboratory equipment and supplies.
- Participate in collaborative research initiatives with external partners and academic institutions.
- Ph.D. in Chemistry, Biology, Physics, Materials Science, or a related scientific discipline.
- A minimum of 5 years of post-doctoral or industry research experience, with a strong track record of independent research.
- Proven experience in experimental design, execution, and data analysis.
- Demonstrated expertise in relevant scientific techniques and instrumentation.
- Strong publication record in peer-reviewed scientific journals.
- Excellent analytical, critical thinking, and problem-solving skills.
- Proficiency in data analysis software and statistical packages (e.g., R, Python, SPSS).
- Exceptional written and verbal communication skills, with the ability to clearly articulate complex scientific concepts.
- Experience working in a hybrid or collaborative team environment, with effective remote communication skills.
- Ability to manage multiple research projects concurrently and meet deadlines.
- A proactive, curious, and self-motivated individual with a passion for scientific innovation.
- Familiarity with intellectual property processes and patent applications is a plus.
- Experience in (Specific Area relevant to R&D, e.g., gene editing, nanoparticle synthesis, quantum computing) is highly desirable.
This advertiser has chosen not to accept applicants from your region.
0
Data Analysis Starter Course (Hiring Immediately)
RG1 1QH Reading, South East
ITonlinelearning Recruitment
Posted today
Job Viewed
Job Description
Data Analyst Course Programme Job Guarantee Included Complete online training designed to take you from zero experience to your first data analyst role. Study part-time, build fundamental skills, and get dedicated job placement support until you're hired. Flexible financing options available, with payment plans starting from as low as 142 per month. The Programme Complete this 10-week online training with just 10-15 hours per week of study time. You'll learn industry-standard tools, including Excel, SQL, Python, and Power BI, while building a professional portfolio with workplace projects. The programme includes earning BCS and CompTIA certifications recognised by UK employers, expert tutor support throughout your studies, and dedicated job placement support with CV help, interview preparation, and direct employer introductions. The Outcome 93% of graduates secure data analyst roles within 3 months. Starting salaries: 28,000 38,000 Who This Is For The programme is completely beginner friendly, so no experience needed. Career changers are welcome, and you can study at your own pace. *This programme is available to UK-based learners only. Ready to start earning in data? Limited spaces available. Apply now for the next available cohort.
This advertiser has chosen not to accept applicants from your region.
1
Data Analysis Starter Course (Hiring Immediately)
OX1 1BX Oxford, South East
ITonlinelearning Recruitment
Posted today
Job Viewed
Job Description
Data Analyst Course Programme Job Guarantee Included Complete online training designed to take you from zero experience to your first data analyst role. Study part-time, build fundamental skills, and get dedicated job placement support until you're hired. Flexible financing options available, with payment plans starting from as low as 142 per month. The Programme Complete this 10-week online training with just 10-15 hours per week of study time. You'll learn industry-standard tools, including Excel, SQL, Python, and Power BI, while building a professional portfolio with workplace projects. The programme includes earning BCS and CompTIA certifications recognised by UK employers, expert tutor support throughout your studies, and dedicated job placement support with CV help, interview preparation, and direct employer introductions. The Outcome 93% of graduates secure data analyst roles within 3 months. Starting salaries: 28,000 38,000 Who This Is For The programme is completely beginner friendly, so no experience needed. Career changers are welcome, and you can study at your own pace. *This programme is available to UK-based learners only. Ready to start earning in data? Limited spaces available. Apply now for the next available cohort.
This advertiser has chosen not to accept applicants from your region.
2
Data Analysis Starter Course (Hiring Immediately)
HP11 2XE High Wycombe, South East
ITonlinelearning Recruitment
Posted today
Job Viewed
Job Description
Data Analyst Course Programme Job Guarantee Included Complete online training designed to take you from zero experience to your first data analyst role. Study part-time, build fundamental skills, and get dedicated job placement support until you're hired. Flexible financing options available, with payment plans starting from as low as 142 per month. The Programme Complete this 10-week online training with just 10-15 hours per week of study time. You'll learn industry-standard tools, including Excel, SQL, Python, and Power BI, while building a professional portfolio with workplace projects. The programme includes earning BCS and CompTIA certifications recognised by UK employers, expert tutor support throughout your studies, and dedicated job placement support with CV help, interview preparation, and direct employer introductions. The Outcome 93% of graduates secure data analyst roles within 3 months. Starting salaries: 28,000 38,000 Who This Is For The programme is completely beginner friendly, so no experience needed. Career changers are welcome, and you can study at your own pace. *This programme is available to UK-based learners only. Ready to start earning in data? Limited spaces available. Apply now for the next available cohort.
This advertiser has chosen not to accept applicants from your region.
3
Senior Geologist - Remote Sensing & Data Analysis
OX1 4AH Oxford, South East
£60000 Annually
WhatJobs
Posted 13 days ago
Job Viewed
Job Description
Our client, a leader in the resource exploration sector, is seeking a highly skilled Senior Geologist with expertise in remote sensing and data analysis for their **Oxford, Oxfordshire, UK** operations. This role offers a hybrid working arrangement, allowing for a blend of remote work and on-site collaboration. The successful candidate will be responsible for interpreting satellite imagery, aerial photography, and other geospatial data to identify potential mineral and hydrocarbon deposits. You will utilize advanced geological modeling software and GIS platforms to create comprehensive prospectivity maps and geological models. Key responsibilities include conducting literature reviews, analyzing geophysical and geochemical data, and contributing to exploration strategy development. The ideal candidate will possess a Master's or Ph.D. in Geology, Geophysics, or a related field, with a strong emphasis on remote sensing techniques and data science. Proven experience with software such as ArcGIS, QGIS, ERDAS IMAGINE, ENVI, and potentially Python or R for data manipulation and analysis is essential. You will be expected to prepare technical reports, present findings to stakeholders, and collaborate effectively with a multidisciplinary team of geologists, geophysicists, and engineers. This position requires excellent analytical skills, a meticulous approach to data interpretation, and the ability to work both independently and as part of a team. A deep understanding of geological principles and exploration methodologies is paramount. This is an exciting opportunity to apply cutting-edge technologies to geological challenges and contribute to significant discoveries. You will be instrumental in guiding exploration efforts and maximizing resource potential through insightful data-driven analysis. The hybrid nature of this role provides flexibility while ensuring critical team synergy.
This advertiser has chosen not to accept applicants from your region.
4
Clinical Research Associate
RG1 2AA Reading, South East
£45000 Annually
WhatJobs
Posted 7 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical innovator, is seeking an experienced Clinical Research Associate (CRA) to join their expanding team in Reading, Berkshire, UK . This role is crucial for overseeing the conduct of clinical trials, ensuring compliance with protocols, and maintaining the integrity of study data. As a CRA, you will be responsible for site selection, initiation, monitoring, and close-out activities. This includes verifying data, ensuring adherence to Good Clinical Practice (GCP) guidelines, and managing relationships with investigators and study staff. The ideal candidate will possess a strong understanding of the drug development process, regulatory requirements, and clinical trial methodologies. You will have excellent communication, interpersonal, and organizational skills, with the ability to manage multiple projects simultaneously. A Bachelor's degree in a life science, nursing, or related field is required, along with significant experience as a CRA, preferably within a pharmaceutical company or Contract Research Organisation (CRO). Responsibilities will include conducting site visits (both remote and on-site), troubleshooting issues, ensuring accurate and timely data collection, and preparing regulatory submissions. The ability to work independently and as part of a collaborative team is essential. This role offers a hybrid working model, blending remote work with essential site visits and team meetings in the Reading office. We are looking for a proactive, detail-oriented individual with a passion for advancing healthcare through robust clinical research. Opportunities for professional growth and development within a supportive and cutting-edge environment are abundant. You will contribute to bringing life-changing therapies to patients worldwide.
This advertiser has chosen not to accept applicants from your region.
5
Clinical Research Associate II
Reading, South East
IQVIA
Posted 13 days ago
Job Viewed
Job Description
**Join Us on Our Mission to Drive Healthcare Forward**
As a Clinical Research Associate at IQVIA, you'll play a vital role in advancing clinical research and improving patient outcomes. We're expanding our Site Management team and looking for passionate CRAs who are ready to make a difference. This role offers a mix of on-site and remote monitoring, supporting work-life balance while contributing to cutting-edge clinical trials.
**Why IQVIA?**
+ IQVIA is recognized as #1 in its category on the 2025 Fortune® World's Most Admired Companies list for the FOURTH consecutive year!
+ We offer genuine career development opportunities for those who want to grow as part of the organization.
+ The chance to work on cutting edge medicines at the forefront of new medicines development.
+ IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!
**Responsibilities**
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
+ Collaborate and liaise with study team members for project execution support as appropriate
**Profile**
+ Over 2 years of independent on-site monitoring experience, ensuring compliance with GCP, protocol requirements, and regulatory guidelines.
+ You have successfully managed multiple clinical trial protocols across diverse investigative sites.
+ Hands-on experience in the Oncology therapeutic area.
+ Flexibility and commitment to nationwide travel
** This role is not eligible for UK Visa Sponsorship**
#LI-AdamThompson
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
As a Clinical Research Associate at IQVIA, you'll play a vital role in advancing clinical research and improving patient outcomes. We're expanding our Site Management team and looking for passionate CRAs who are ready to make a difference. This role offers a mix of on-site and remote monitoring, supporting work-life balance while contributing to cutting-edge clinical trials.
**Why IQVIA?**
+ IQVIA is recognized as #1 in its category on the 2025 Fortune® World's Most Admired Companies list for the FOURTH consecutive year!
+ We offer genuine career development opportunities for those who want to grow as part of the organization.
+ The chance to work on cutting edge medicines at the forefront of new medicines development.
+ IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!
**Responsibilities**
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
+ Collaborate and liaise with study team members for project execution support as appropriate
**Profile**
+ Over 2 years of independent on-site monitoring experience, ensuring compliance with GCP, protocol requirements, and regulatory guidelines.
+ You have successfully managed multiple clinical trial protocols across diverse investigative sites.
+ Hands-on experience in the Oncology therapeutic area.
+ Flexibility and commitment to nationwide travel
** This role is not eligible for UK Visa Sponsorship**
#LI-AdamThompson
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This advertiser has chosen not to accept applicants from your region.
Be The First To Know
About the latest Researchers Jobs in Oxford !
6
Experienced Clinical Research Associate
Reading, South East
IQVIA
Posted 13 days ago
Job Viewed
Job Description
Join Us on Our Mission to Drive Healthcare Forward
IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.
Why IQVIA?
+ IQVIA is recognized as #1 in its category on the 2025 Fortune® World's Most Admired Companies list for the FOURTH consecutive year!
+ We offer genuine career development opportunities for those who want to grow as part of the organization.
+ The chance to work on cutting edge medicines at the forefront of new medicines development.
+ IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!
Responsibilities
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
+ Collaborate and liaise with study team members for project execution support as appropriate
Requirements
+ Experience of independent on-site monitoring
+ You have successfully managed multiple clinical trial protocols across diverse investigative sites.
+ In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Life science degree educated or equivalent industry experience
+ Flexibility to travel to sites
Apply today and forge a career with greater purpose, make an impact, and never stop learning!
#LI-ADAMTHOMPSON
*Please note - this role is not eligible for UK visa sponsorship*
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.
Why IQVIA?
+ IQVIA is recognized as #1 in its category on the 2025 Fortune® World's Most Admired Companies list for the FOURTH consecutive year!
+ We offer genuine career development opportunities for those who want to grow as part of the organization.
+ The chance to work on cutting edge medicines at the forefront of new medicines development.
+ IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!
Responsibilities
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
+ Collaborate and liaise with study team members for project execution support as appropriate
Requirements
+ Experience of independent on-site monitoring
+ You have successfully managed multiple clinical trial protocols across diverse investigative sites.
+ In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Life science degree educated or equivalent industry experience
+ Flexibility to travel to sites
Apply today and forge a career with greater purpose, make an impact, and never stop learning!
#LI-ADAMTHOMPSON
*Please note - this role is not eligible for UK visa sponsorship*
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This advertiser has chosen not to accept applicants from your region.
7
Clinical Research Associate (CRA)
OX1 1 Oxford, South East
£45000 Annually
WhatJobs
Posted 11 days ago
Job Viewed
Job Description
Our client, a prominent pharmaceutical company, is seeking a dedicated and meticulous Clinical Research Associate (CRA) to join their expanding team. This role will involve monitoring clinical trial sites to ensure compliance with protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. You will be responsible for site initiation, monitoring, and close-out activities, as well as building strong relationships with investigators and site staff. The ideal candidate will possess a strong understanding of clinical trial processes, excellent organizational skills, and the ability to travel to sites.
Responsibilities:
Responsibilities:
- Perform site initiation, monitoring, and close-out visits in accordance with approved study plans.
- Ensure adherence to study protocols, Standard Operating Procedures (SOPs), and applicable regulations.
- Verify the accuracy, completeness, and integrity of clinical data through source document verification.
- Identify, document, and escalate study-related issues and deviations.
- Train and support site staff on study procedures and regulatory requirements.
- Manage study supplies and investigational product accountability.
- Communicate effectively with study team members, investigators, and site personnel.
- Prepare and submit monitoring reports in a timely manner.
- Contribute to the development and review of study-related documents.
- Ensure patient safety and data quality throughout the trial lifecycle.
- Bachelor's degree in a life science, nursing, or related field; advanced degree preferred.
- Minimum of 2-3 years of experience as a Clinical Research Associate or in a similar clinical trial role.
- Thorough understanding of GCP, ICH guidelines, and regulatory requirements.
- Experience in site monitoring and data verification.
- Excellent communication, interpersonal, and organizational skills.
- Ability to travel to clinical trial sites as required.
- Proficiency in clinical trial management systems (CTMS) and Electronic Data Capture (EDC) systems.
- Strong attention to detail and ability to manage multiple tasks simultaneously.
This advertiser has chosen not to accept applicants from your region.
8
Clinical Research Associate (CRA)
RG1 1FF Reading, South East
£45000 Annually
WhatJobs
Posted 11 days ago
Job Viewed
Job Description
Our client, a pioneering pharmaceutical company dedicated to advancing global health, is seeking a highly motivated and experienced Clinical Research Associate (CRA) to join their fully remote global team. This role is crucial in overseeing clinical trials, ensuring adherence to protocols, and maintaining data integrity. You will play a vital part in bringing life-changing treatments to patients worldwide. This is a remote-first opportunity, allowing you to work from your home office.
Responsibilities:
Qualifications:
This position is based in Reading, Berkshire, UK , but is structured as a fully remote role, providing significant flexibility. If you are a dedicated CRA passionate about making a difference in pharmaceutical research, we encourage you to apply for this exciting remote opportunity.
Responsibilities:
- Conduct site selection, initiation, monitoring, and close-out visits for clinical trial sites in accordance with protocol and GCP guidelines.
- Ensure compliance with study protocols, regulatory requirements, and ethical standards.
- Verify the accuracy, completeness, and integrity of clinical data through source document verification.
- Manage and maintain essential regulatory documents at study sites.
- Serve as the primary liaison between the sponsor and the clinical trial sites.
- Identify, document, and escalate study-related issues and risks to project management.
- Train and support site staff on study procedures and data collection requirements.
- Ensure timely submission of study reports and other required documentation.
- Participate in investigator meetings and teleconferences as required.
- Contribute to the development and review of study-related documents.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field; Advanced degree preferred.
- Minimum of 3 years of experience as a Clinical Research Associate, with a strong understanding of ICH-GCP guidelines.
- Proven experience in monitoring clinical trials across various therapeutic areas.
- Excellent knowledge of regulatory requirements and drug development processes.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Strong analytical, problem-solving, and organisational skills.
- Exceptional written and verbal communication skills, with the ability to interact effectively with healthcare professionals.
- Ability to work independently, manage time effectively, and travel as required (approximately 50-70% travel).
- A meticulous approach to documentation and a commitment to data quality.
- Must be legally authorised to work in the UK and currently reside within.
This position is based in Reading, Berkshire, UK , but is structured as a fully remote role, providing significant flexibility. If you are a dedicated CRA passionate about making a difference in pharmaceutical research, we encourage you to apply for this exciting remote opportunity.
This advertiser has chosen not to accept applicants from your region.
9