107 Clinical Research Associates jobs in London
Research Assistant/Clinical Research Coordinator - London
Posted 14 days ago
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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.
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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.
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Clinical Research Scientist
Posted 19 days ago
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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.
Clinical Research Associate I
Posted today
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Clinical Research Associate I
Posted today
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Clinical Research Associate I
Posted today
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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
Senior Clinical Research Associate
Posted 1 day ago
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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.
Senior Clinical Research Associate
Posted 14 days ago
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Remote Clinical Research Associate
Posted 19 days ago
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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.
Senior Clinical Research Associate
Posted 19 days ago
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Job Description
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.
Clinical Research Associate (CRA)
Posted 19 days ago
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Job Description
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.