107 Clinical Research Associates jobs in London
Research Assistant/Clinical Research Coordinator - London
London, London
IQVIA
Posted 14 days ago
Job Viewed
Job Description
Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company that offers you an excellent benefits package and supports career progression whilst giving you the option of working flexibly? If so, come and join us - IQVIA are looking for a Research Assistant/Study Coordinator.
This role is to support the site in **London** in conducting a clinical trial for **8** hours per week.
As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.
**Day to day responsibilities will include:**
+ Support clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator
+ Safeguard the well-being of subjects, act as a volunteer advocate, and address subject's concerns
+ Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
+ Plan and coordinate logistical activity for study procedures according to the study protocol
+ Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and/or study issues
+ Assist with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
+ Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol
+ Correct custody of study drug according to site standard operating procedures
+ Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions.
**We are looking for candidates with the following skills and experience:**
+ Two years of experience with clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
+ Basic knowledge of medical terminology
+ Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
+ Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and client
+ Good organizational skills with the ability to pay close attention to detail.
#LI-DNP
#LI-CES
#LI-HCPN
#LI-CT1
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 role is to support the site in **London** in conducting a clinical trial for **8** hours per week.
As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.
**Day to day responsibilities will include:**
+ Support clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator
+ Safeguard the well-being of subjects, act as a volunteer advocate, and address subject's concerns
+ Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
+ Plan and coordinate logistical activity for study procedures according to the study protocol
+ Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and/or study issues
+ Assist with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
+ Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol
+ Correct custody of study drug according to site standard operating procedures
+ Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions.
**We are looking for candidates with the following skills and experience:**
+ Two years of experience with clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
+ Basic knowledge of medical terminology
+ Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
+ Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and client
+ Good organizational skills with the ability to pay close attention to detail.
#LI-DNP
#LI-CES
#LI-HCPN
#LI-CT1
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.
0
Clinical Research Scientist
SW1A 0AA London, London
£65000 Annually
WhatJobs
Posted 19 days ago
Job Viewed
Job Description
Our client, a pioneering pharmaceutical company, is looking for an innovative Clinical Research Scientist to contribute to groundbreaking drug development from the comfort of their home. This is a fully remote position, offering the flexibility to work from anywhere within the UK, with a focus on designing and executing clinical trials that will shape the future of medicine. You will be responsible for the scientific integrity of clinical studies, from protocol development through to final study report.
Key responsibilities include analyzing complex data sets, interpreting results, and presenting findings to internal stakeholders and regulatory bodies. You will collaborate closely with cross-functional teams, including statisticians, medical writers, and regulatory affairs specialists, to ensure compliance with all relevant guidelines and regulations. This role demands a deep understanding of pharmaceutical research methodologies, statistical analysis, and regulatory requirements (e.g., GCP, ICH). A PhD or equivalent in a relevant life science discipline (e.g., pharmacology, biochemistry, molecular biology) is highly preferred, along with a proven track record of successfully managing clinical trials.
The ideal candidate will possess exceptional analytical skills, a meticulous attention to detail, and the ability to work independently with minimal supervision. Strong written and verbal communication skills are essential for documenting research, writing manuscripts for publication, and presenting scientific information clearly and concisely. You should be adept at managing multiple projects simultaneously and meeting tight deadlines. This is an exceptional opportunity to join a forward-thinking organization and make a significant impact on global health, working on cutting-edge therapies. Your expertise will be crucial in bringing life-changing treatments to patients worldwide. Embrace the future of pharmaceutical research in this exciting remote role.
Key responsibilities include analyzing complex data sets, interpreting results, and presenting findings to internal stakeholders and regulatory bodies. You will collaborate closely with cross-functional teams, including statisticians, medical writers, and regulatory affairs specialists, to ensure compliance with all relevant guidelines and regulations. This role demands a deep understanding of pharmaceutical research methodologies, statistical analysis, and regulatory requirements (e.g., GCP, ICH). A PhD or equivalent in a relevant life science discipline (e.g., pharmacology, biochemistry, molecular biology) is highly preferred, along with a proven track record of successfully managing clinical trials.
The ideal candidate will possess exceptional analytical skills, a meticulous attention to detail, and the ability to work independently with minimal supervision. Strong written and verbal communication skills are essential for documenting research, writing manuscripts for publication, and presenting scientific information clearly and concisely. You should be adept at managing multiple projects simultaneously and meeting tight deadlines. This is an exceptional opportunity to join a forward-thinking organization and make a significant impact on global health, working on cutting-edge therapies. Your expertise will be crucial in bringing life-changing treatments to patients worldwide. Embrace the future of pharmaceutical research in this exciting remote role.
This advertiser has chosen not to accept applicants from your region.
1
Clinical Research Associate I
London, London
Russell Tobin
Posted today
Job Viewed
Job Description
Job title: Clinical Project Associate I Location: London Contract duration: 12 months Client: Pharmaceutical Job Purpose: The Project Associate (PA) supports the planning and execution of multiple clinical development initiatives. Working closely with Clinical Development colleagues and cross-functional stakeholders, the PA drives operational efficiency and contributes to successful project delivery. The role ensures project activities are well-organized, deadlines are met, and communication flows effectively. Major Activities: • Project Planning, Coordination and Execution: Develop and maintain detailed project timelines, and contribute to content of key deliverables. Ensure all aspects of the project are organized and tracked effectively. Monitor completion status of deliverables, flag issues and opportunities, and escalate as needed. Ensure team is working in alignment with project objectives. Maintain project dashboards and support reporting for governance reviews. • Documentation Management: Maintain and manage project documents, reports, and meeting agendas/minutes, ensuring that all records are accurate and accessible. • Meeting Preparation & Facilitation: Schedule, prepare, and co-facilitate project meetings and workshops, ensuring adherence to meeting excellence standards (agenda, minutes, action items) • Communication: Act as a liaison between project teams and stakeholders, facilitating seamless information flow and collaboration. • Content creation: Creation of structured content in PowerPoint to support project needs and communication with project teams and stakeholders. • Quality Assurance: Monitor project deliverables to ensure they meet predefined quality standards. Contribute to continuous improvement initiatives and process optimization. • Risk Management: Identify potential risks in project execution and collaborate with the team to develop strategies to mitigate these risks. • Data Analysis: Analyze project-related data to extract insights that support informed decision-making. Contribute to benchmarking and background research on regulatory landscapes and industry practices. Primary focus will be supporting the Protocol Design Excellence (PDE) team within the Clinical Science group. Education and/or professional experience: • Bachelor’s degree in life sciences, public health, or a related field. Languages: • Fluent English (oral and written) Experience / Professional Requirements: • 2-3 years of experience in clinical research, project coordination or consultancy. • Understanding of Drug Development processes and familiarity with clinical trial processes and regulatory frameworks • Strong organisational, project management and communication skills. • Proficiency in Microsoft Office and project management tools. • Delivery focus; reliable and respond promptly to requests • Ability to multi-task and prioritize • Strong attention to detail and highly organized • Successful relationship builder and communicator • Ability to work independently and collaboratively in a fast-paced environment. • Desirable: Experience with AI tools in clinical development
This advertiser has chosen not to accept applicants from your region.
2
Clinical Research Associate I
London, London
Russell Tobin
Posted today
Job Viewed
Job Description
Job title: Clinical Project Associate I Location: London Contract duration: 12 months Client: Pharmaceutical Job Purpose: The Project Associate (PA) supports the planning and execution of multiple clinical development initiatives. Working closely with Clinical Development colleagues and cross-functional stakeholders, the PA drives operational efficiency and contributes to successful project delivery. The role ensures project activities are well-organized, deadlines are met, and communication flows effectively. Major Activities: • Project Planning, Coordination and Execution: Develop and maintain detailed project timelines, and contribute to content of key deliverables. Ensure all aspects of the project are organized and tracked effectively. Monitor completion status of deliverables, flag issues and opportunities, and escalate as needed. Ensure team is working in alignment with project objectives. Maintain project dashboards and support reporting for governance reviews. • Documentation Management: Maintain and manage project documents, reports, and meeting agendas/minutes, ensuring that all records are accurate and accessible. • Meeting Preparation & Facilitation: Schedule, prepare, and co-facilitate project meetings and workshops, ensuring adherence to meeting excellence standards (agenda, minutes, action items) • Communication: Act as a liaison between project teams and stakeholders, facilitating seamless information flow and collaboration. • Content creation: Creation of structured content in PowerPoint to support project needs and communication with project teams and stakeholders. • Quality Assurance: Monitor project deliverables to ensure they meet predefined quality standards. Contribute to continuous improvement initiatives and process optimization. • Risk Management: Identify potential risks in project execution and collaborate with the team to develop strategies to mitigate these risks. • Data Analysis: Analyze project-related data to extract insights that support informed decision-making. Contribute to benchmarking and background research on regulatory landscapes and industry practices. Primary focus will be supporting the Protocol Design Excellence (PDE) team within the Clinical Science group. Education and/or professional experience: • Bachelor’s degree in life sciences, public health, or a related field. Languages: • Fluent English (oral and written) Experience / Professional Requirements: • 2-3 years of experience in clinical research, project coordination or consultancy. • Understanding of Drug Development processes and familiarity with clinical trial processes and regulatory frameworks • Strong organisational, project management and communication skills. • Proficiency in Microsoft Office and project management tools. • Delivery focus; reliable and respond promptly to requests • Ability to multi-task and prioritize • Strong attention to detail and highly organized • Successful relationship builder and communicator • Ability to work independently and collaboratively in a fast-paced environment. • Desirable: Experience with AI tools in clinical development
This advertiser has chosen not to accept applicants from your region.
3
Clinical Research Associate I
London, London
Russell Tobin
Posted today
Job Viewed
Job Description
Job title: Clinical Project Associate I
Location: London
Contract duration: 12 months
Client: Pharmaceutical
Job Purpose:
The Project Associate (PA) supports the planning and execution of multiple clinical development initiatives. Working closely with Clinical Development colleagues and cross-functional stakeholders, the PA drives operational efficiency and contributes to successful project delivery. The role ensures project activities are well-organized, deadlines are met, and communication flows effectively.
Major Activities:
• Project Planning, Coordination and Execution: Develop and maintain detailed project timelines, and contribute to content of key deliverables. Ensure all aspects of the project are organized and tracked effectively. Monitor completion status of deliverables, flag issues and opportunities, and escalate as needed. Ensure team is working in alignment with project objectives. Maintain project dashboards and support reporting for governance reviews.
• Documentation Management: Maintain and manage project documents, reports, and meeting agendas/minutes, ensuring that all records are accurate and accessible.
• Meeting Preparation & Facilitation: Schedule, prepare, and co-facilitate project meetings and workshops, ensuring adherence to meeting excellence standards (agenda, minutes, action items)
• Communication: Act as a liaison between project teams and stakeholders, facilitating seamless information flow and collaboration.
• Content creation: Creation of structured content in PowerPoint to support project needs and communication with project teams and stakeholders.
• Quality Assurance: Monitor project deliverables to ensure they meet predefined quality standards. Contribute to continuous improvement initiatives and process optimization.
• Risk Management: Identify potential risks in project execution and collaborate with the team to develop strategies to mitigate these risks.
• Data Analysis: Analyze project-related data to extract insights that support informed decision-making. Contribute to benchmarking and background research on regulatory landscapes and industry practices.
Primary focus will be supporting the Protocol Design Excellence (PDE) team within the Clinical Science group.
Education and/or professional experience:
• Bachelor’s degree in life sciences, public health, or a related field.
Languages:
• Fluent English (oral and written)
Experience / Professional Requirements:
• 2-3 years of experience in clinical research, project coordination or consultancy.
• Understanding of Drug Development processes and familiarity with clinical trial processes and regulatory frameworks
• Strong organisational, project management and communication skills.
• Proficiency in Microsoft Office and project management tools.
• Delivery focus; reliable and respond promptly to requests
• Ability to multi-task and prioritize
• Strong attention to detail and highly organized
• Successful relationship builder and communicator
• Ability to work independently and collaboratively in a fast-paced environment.
• Desirable: Experience with AI tools in clinical development
This advertiser has chosen not to accept applicants from your region.
4
Senior Clinical Research Associate
SW1A 0AA London, London
£65000 Annually
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client , a leading pharmaceutical innovator, is seeking a highly skilled and motivated Senior Clinical Research Associate (CRA) to join their dynamic team in London, England, UK . This pivotal role will involve overseeing and managing clinical trials, ensuring adherence to protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. The Senior CRA will be responsible for site selection, initiation, monitoring, and close-out activities. You will serve as the primary point of contact for clinical investigators and site staff, providing essential support and guidance.
Key responsibilities include developing and implementing clinical trial monitoring plans, conducting regular site visits (both in-person and remote), verifying the accuracy and completeness of source data, and ensuring the timely submission of essential documents. You will also be instrumental in identifying and resolving site-level issues, preparing and presenting monitoring reports, and ensuring that all trial-related activities are conducted ethically and in accordance with ethical principles and patient safety standards. Collaboration with cross-functional teams, including data management, biostatistics, and regulatory affairs, is crucial for the successful execution of trials. The ideal candidate will possess strong leadership qualities, excellent communication and interpersonal skills, and a meticulous attention to detail. A proven track record in managing multiple complex clinical trials simultaneously is essential. This role offers an exciting opportunity to contribute to groundbreaking medical advancements within a supportive and progressive work environment. We are looking for an individual with a deep understanding of the drug development process and a passion for improving patient outcomes.
Qualifications:
Key responsibilities include developing and implementing clinical trial monitoring plans, conducting regular site visits (both in-person and remote), verifying the accuracy and completeness of source data, and ensuring the timely submission of essential documents. You will also be instrumental in identifying and resolving site-level issues, preparing and presenting monitoring reports, and ensuring that all trial-related activities are conducted ethically and in accordance with ethical principles and patient safety standards. Collaboration with cross-functional teams, including data management, biostatistics, and regulatory affairs, is crucial for the successful execution of trials. The ideal candidate will possess strong leadership qualities, excellent communication and interpersonal skills, and a meticulous attention to detail. A proven track record in managing multiple complex clinical trials simultaneously is essential. This role offers an exciting opportunity to contribute to groundbreaking medical advancements within a supportive and progressive work environment. We are looking for an individual with a deep understanding of the drug development process and a passion for improving patient outcomes.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related discipline. Advanced degree preferred.
- Minimum of 5 years of direct experience as a Clinical Research Associate in the pharmaceutical or biotech industry.
- Comprehensive knowledge of ICH-GCP guidelines, FDA regulations, and other relevant regulatory requirements.
- Demonstrated experience in managing all phases of clinical trials.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Excellent written and verbal communication skills, with the ability to present complex information clearly and concisely.
- Strong analytical and problem-solving abilities.
- Ability to travel as required for site visits and team meetings.
This advertiser has chosen not to accept applicants from your region.
5
Senior Clinical Research Associate
SW1A 0AA London, London
£55000 Annually
WhatJobs
Posted 14 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking an experienced Senior Clinical Research Associate (CRA) to join their dedicated team based in London, England, UK . This critical role involves overseeing and managing clinical trials, ensuring compliance with regulatory standards and protocol requirements. You will be responsible for site selection, initiation, monitoring, and close-out activities, building strong relationships with investigators and site staff. The ideal candidate will have a deep understanding of Good Clinical Practice (GCP) guidelines and experience with various therapeutic areas. Your responsibilities will include conducting site visits to assess patient safety, data integrity, and overall trial progress. You will also be involved in preparing study documentation, managing investigational product, and ensuring timely data collection and query resolution. Excellent communication, organisational, and problem-solving skills are essential for this role, as is the ability to work independently and as part of a wider clinical operations team. A Bachelor's degree in a life science, nursing, or a related field is required. A Master's degree or equivalent experience is highly desirable. Significant prior experience as a CRA, with a proven track record of successful trial management, is mandatory. Experience in oncology, cardiology, or another relevant therapeutic area would be advantageous. The ability to travel extensively (up to 60%) for site visits is required. This is an excellent opportunity to contribute to the development of life-saving medicines within a respected pharmaceutical organisation.
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6
Remote Clinical Research Associate
WC2N 5DU London, London
£45000 Annually
WhatJobs
Posted 19 days ago
Job Viewed
Job Description
Our client, a leading global pharmaceutical company with a significant presence in London, England, UK , is seeking a highly qualified and meticulous Remote Clinical Research Associate (CRA) to support their groundbreaking research initiatives. This is a fully remote position, offering the opportunity to contribute to vital drug development from anywhere within the UK. You will be responsible for monitoring clinical trial sites, ensuring data integrity, and verifying compliance with regulatory requirements and study protocols. The ideal candidate possesses a strong scientific background, a thorough understanding of GCP guidelines, and exceptional organisational and analytical skills. This role is critical in ensuring the accuracy, validity, and timeliness of clinical trial data, contributing directly to the advancement of life-saving treatments.
Key responsibilities include:
To be successful in this role, you must have a Bachelor's degree in a life science, nursing, or related field. A minimum of 3 years of experience as a Clinical Research Associate, with proven experience in remote monitoring, is essential. A comprehensive understanding of Good Clinical Practice (GCP) and regulatory guidelines (e.g., FDA, EMA) is mandatory. Excellent analytical, problem-solving, and communication skills are required, along with the ability to work independently and manage multiple priorities effectively. Proficiency with clinical trial management systems (CTMS) and EDC systems is expected. This is a fantastic opportunity for an experienced CRA to join a world-class organisation and play a key role in bringing innovative pharmaceutical products to market, all within a flexible remote working arrangement.
Key responsibilities include:
- Performing remote site monitoring activities to ensure compliance with study protocols, SOPs, and GCP.
- Reviewing and verifying source documents, case report forms (CRFs), and electronic data capture (EDC) systems.
- Assessing the quality and integrity of data collected at clinical trial sites.
- Identifying and reporting potential protocol deviations and adverse events.
- Managing communication between study sites, investigators, and internal project teams.
- Ensuring site readiness for audits and regulatory inspections.
- Supporting site initiation, monitoring visits, and site closure activities.
- Maintaining accurate and up-to-date trial documentation and databases.
- Providing training and guidance to site staff on study-related procedures.
- Contributing to the development and review of study-related documents.
To be successful in this role, you must have a Bachelor's degree in a life science, nursing, or related field. A minimum of 3 years of experience as a Clinical Research Associate, with proven experience in remote monitoring, is essential. A comprehensive understanding of Good Clinical Practice (GCP) and regulatory guidelines (e.g., FDA, EMA) is mandatory. Excellent analytical, problem-solving, and communication skills are required, along with the ability to work independently and manage multiple priorities effectively. Proficiency with clinical trial management systems (CTMS) and EDC systems is expected. This is a fantastic opportunity for an experienced CRA to join a world-class organisation and play a key role in bringing innovative pharmaceutical products to market, all within a flexible remote working arrangement.
This advertiser has chosen not to accept applicants from your region.
7
Senior Clinical Research Associate
SW1A 0AA London, London
£55000 Annually
WhatJobs
Posted 19 days ago
Job Viewed
Job Description
Our client is seeking a highly experienced and motivated Senior Clinical Research Associate (CRA) to join their dynamic pharmaceutical team based in London, England, UK . This role offers a hybrid working model, blending remote flexibility with essential on-site collaboration. As a Senior CRA, you will play a critical role in the planning, execution, and monitoring of clinical trials, ensuring adherence to protocols, regulatory requirements, and good clinical practice (GCP).
Key Responsibilities:
Key Responsibilities:
- Initiate, monitor, and close clinical trial sites, ensuring all trial activities are conducted according to the protocol, standard operating procedures (SOPs), and regulatory guidelines.
- Perform site visits, including pre-study, initiation, monitoring, and close-out visits, as required.
- Assess protocol compliance, including patient recruitment, informed consent process, and data accuracy.
- Ensure timely resolution of site issues and discrepancies.
- Train and mentor junior CRAs and site staff on protocol requirements and study procedures.
- Prepare and present study progress reports to project management and relevant stakeholders.
- Manage relationships with investigators, site staff, and other study vendors.
- Oversee drug accountability and investigational product management at trial sites.
- Ensure accurate and timely source data verification (SDV) and review of case report forms (CRFs).
- Contribute to the development and review of study-related documents, such as investigator brochures, protocols, and informed consent forms.
- Act as a key point of contact between the sponsor and the clinical trial sites.
- Bachelor's degree in life sciences, nursing, or a related field; advanced degree preferred.
- Minimum of 5 years of experience as a Clinical Research Associate in the pharmaceutical industry.
- In-depth knowledge of ICH-GCP guidelines, local regulatory requirements, and clinical trial processes.
- Proven experience in monitoring various phases of clinical trials.
- Strong understanding of medical terminology and disease areas relevant to pharmaceutical research.
- Excellent communication, interpersonal, and organizational skills.
- Ability to work independently and as part of a team, with a proactive and detail-oriented approach.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Willingness to travel to sites as needed.
This advertiser has chosen not to accept applicants from your region.
8
Clinical Research Associate (CRA)
WC2H 7LP London, London
£50000 Annually
WhatJobs
Posted 19 days ago
Job Viewed
Job Description
Our client, a leading global pharmaceutical company, is seeking a highly motivated and experienced Clinical Research Associate (CRA) to join their dynamic team. This role is essential for ensuring the successful execution of clinical trials in compliance with Good Clinical Practice (GCP) guidelines and regulatory requirements. You will be responsible for monitoring investigational sites, ensuring the quality and integrity of data collected, and verifying patient safety throughout the trial process. This hybrid role combines remote administrative tasks with on-site visits to clinical trial sites.
Key responsibilities include site selection, initiation, monitoring, and close-out visits. You will assess protocol adherence, verify source data, and ensure accurate and timely entry of data into clinical trial databases. Building and maintaining strong working relationships with investigators, site staff, and internal project teams is crucial. You will be responsible for resolving data queries, managing site supplies, and ensuring all regulatory documentation is up-to-date and accurately maintained. Adherence to study protocols, ethical principles, and company policies is paramount.
The ideal candidate will possess a Bachelor's degree in a life science, nursing, or a related field, with a minimum of 2-4 years of experience as a CRA or in a similar clinical research role. A thorough understanding of GCP, ICH guidelines, and regulatory requirements in the pharmaceutical industry is essential. Excellent communication, organizational, and time management skills are required, along with strong attention to detail and the ability to work independently. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is highly desirable. This role is based in the London, England, UK area, offering a hybrid working model that provides flexibility while ensuring necessary on-site engagement. If you are a dedicated professional committed to advancing medical research and patient care, we encourage you to apply.
Key responsibilities include site selection, initiation, monitoring, and close-out visits. You will assess protocol adherence, verify source data, and ensure accurate and timely entry of data into clinical trial databases. Building and maintaining strong working relationships with investigators, site staff, and internal project teams is crucial. You will be responsible for resolving data queries, managing site supplies, and ensuring all regulatory documentation is up-to-date and accurately maintained. Adherence to study protocols, ethical principles, and company policies is paramount.
The ideal candidate will possess a Bachelor's degree in a life science, nursing, or a related field, with a minimum of 2-4 years of experience as a CRA or in a similar clinical research role. A thorough understanding of GCP, ICH guidelines, and regulatory requirements in the pharmaceutical industry is essential. Excellent communication, organizational, and time management skills are required, along with strong attention to detail and the ability to work independently. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is highly desirable. This role is based in the London, England, UK area, offering a hybrid working model that provides flexibility while ensuring necessary on-site engagement. If you are a dedicated professional committed to advancing medical research and patient care, we encourage you to apply.
This advertiser has chosen not to accept applicants from your region.
9