557 Clinical Research Associates jobs in the United Kingdom
Clinical Research Coordinator
NR1 1AA Norwich, Eastern
£35000 Annually
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Posted 3 days ago
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Job Description
Our client, a reputable healthcare research organization, is seeking an experienced Clinical Research Coordinator to join their dedicated team in **Norwich, Norfolk, UK**. This role is essential for the successful planning, implementation, and execution of clinical trials. The Clinical Research Coordinator will work closely with principal investigators, study participants, and regulatory bodies to ensure trials are conducted according to protocol, ethical standards, and regulatory requirements. The position requires a detail-oriented individual with strong organizational and communication skills, and a commitment to advancing medical knowledge through rigorous research.
Key Responsibilities:
Key Responsibilities:
- Recruit, screen, and enroll eligible participants for clinical trials.
- Obtain informed consent from participants, ensuring they understand the study procedures, risks, and benefits.
- Collect, manage, and process study data accurately and efficiently, maintaining case report forms (CRFs) and electronic data capture (EDC) systems.
- Monitor participants' progress throughout the trial, documenting any adverse events or deviations from protocol.
- Ensure compliance with Good Clinical Practice (GCP) guidelines, FDA regulations, and other relevant ethical and regulatory standards.
- Schedule and coordinate participant appointments, laboratory tests, and other study-related procedures.
- Maintain accurate and organized study files, including essential documents, regulatory binders, and source documentation.
- Liaise with investigators, study sponsors, contract research organizations (CROs), and Institutional Review Boards (IRBs)/Ethics Committees.
- Assist in the preparation of study protocols, amendments, and reports.
- Manage study supplies and equipment, ensuring their availability and proper functioning.
- Participate in study initiation, monitoring, and close-out visits.
- Contribute to a safe and efficient research environment.
- Bachelor's degree in a life science, nursing, or related healthcare field.
- Previous experience working as a Clinical Research Coordinator or in a similar clinical research role is required.
- In-depth knowledge of GCP guidelines, clinical trial processes, and regulatory requirements.
- Experience with EDC systems and clinical data management is essential.
- Excellent organizational, time management, and multitasking abilities.
- Strong interpersonal and communication skills, with the ability to interact effectively with participants, healthcare professionals, and sponsors.
- Proficiency in Microsoft Office Suite.
- Attention to detail and commitment to accuracy.
- Ability to work independently and as part of a team in a fast-paced research setting.
- Certification as a Clinical Research Professional (e.g., SoCRA, ACRP) is a significant advantage.
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0
Remote Clinical Research Coordinator
AB10 1QR Aberdeen, Scotland
£35000 Annually
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Posted today
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Job Description
Our client, a progressive organization dedicated to advancing healthcare solutions, is seeking a meticulous and organized Remote Clinical Research Coordinator to join their innovative team. This role is fully remote, enabling you to contribute to groundbreaking research from the convenience of your home office. You will be responsible for managing and coordinating all aspects of clinical trials, ensuring compliance with study protocols, regulatory requirements, and ethical standards. Your dedication to accuracy and patient safety will be paramount. Key responsibilities include:
Qualifications:
This is a rewarding opportunity to contribute to vital medical advancements while enjoying the flexibility of remote work. Make a difference in the field of community and social care research from your home, supporting initiatives that impact lives globally, including those managed by our client near Aberdeen, Scotland, UK .
- Coordinating all study-related activities, including patient recruitment, screening, scheduling, and follow-up visits.
- Obtaining informed consent from study participants and ensuring their understanding of study procedures.
- Collecting, documenting, and managing clinical data accurately and efficiently using electronic data capture (EDC) systems.
- Monitoring patient adherence to study protocols and reporting any adverse events or protocol deviations promptly.
- Maintaining comprehensive and organized study documentation, including regulatory binders and source documents.
- Liaising with investigators, research staff, sponsors, and regulatory authorities.
- Assisting with site initiation visits, monitoring visits, and close-out visits as required.
- Ensuring compliance with Good Clinical Practice (GCP) guidelines and other relevant regulations.
- Managing study supplies and investigational products.
- Educating patients and their families about the clinical trial.
- Participating in team meetings and contributing to the continuous improvement of clinical research processes.
Qualifications:
- A Bachelor's degree in a life science, nursing, or a related healthcare field.
- Previous experience as a Clinical Research Coordinator or in a similar clinical research role.
- Thorough understanding of GCP guidelines, clinical trial processes, and regulatory requirements.
- Proficiency with EDC systems and other clinical trial management software.
- Excellent organizational, time management, and multitasking skills.
- Strong attention to detail and commitment to data accuracy.
- Exceptional interpersonal and communication skills, with the ability to interact professionally with patients, healthcare providers, and study sponsors.
- Ability to work independently and manage workload effectively in a remote environment.
- Strong problem-solving abilities and a proactive approach.
This is a rewarding opportunity to contribute to vital medical advancements while enjoying the flexibility of remote work. Make a difference in the field of community and social care research from your home, supporting initiatives that impact lives globally, including those managed by our client near Aberdeen, Scotland, UK .
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1
Senior Clinical Research Coordinator
S1 4QX Sheffield, Yorkshire and the Humber
£50000 Annually
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Posted 3 days ago
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Job Description
Our client, a leading organization in community health and social care innovation, is seeking a dedicated and experienced Senior Clinical Research Coordinator to lead and manage clinical research projects within their fully remote framework. This crucial role involves overseeing all aspects of research studies, ensuring compliance with ethical standards, regulatory requirements, and institutional policies. The ideal candidate will possess a strong background in clinical research methodologies, project management, and stakeholder engagement.
Responsibilities:
This is a unique opportunity for a seasoned clinical research professional to make a significant impact while enjoying the flexibility of a fully remote role. Contribute to vital research initiatives that enhance community well-being from the comfort of your home. Our client is dedicated to improving healthcare outcomes through evidence-based practice and innovation. We offer a supportive and dynamic work environment, emphasizing professional growth and work-life balance. This role is notionally based in Sheffield, South Yorkshire, UK , but operates as a fully remote position. We are committed to creating an inclusive and diverse workforce.
Qualifications:
Responsibilities:
- Lead the planning, execution, and monitoring of clinical research studies from initiation to closure.
- Ensure all research activities are conducted in compliance with Good Clinical Practice (GCP) guidelines, ethical principles, and relevant regulations.
- Develop and manage study protocols, informed consent forms, and other essential research documents.
- Recruit, train, and supervise research staff, fostering a collaborative and high-performing team environment.
- Oversee patient recruitment and enrollment, ensuring adherence to eligibility criteria.
- Manage data collection, entry, and quality control processes, ensuring accuracy and completeness.
- Liaise with investigators, study sponsors, regulatory agencies, and ethics committees.
- Monitor study progress, identify potential risks, and implement mitigation strategies.
- Manage study budgets and resources effectively.
- Prepare study reports and contribute to research publications.
- Maintain accurate and organized study files and records.
- Stay updated on the latest advancements and best practices in clinical research and healthcare.
- Facilitate effective communication among all study stakeholders.
- Promote a culture of ethical conduct and patient safety throughout all research endeavors.
This is a unique opportunity for a seasoned clinical research professional to make a significant impact while enjoying the flexibility of a fully remote role. Contribute to vital research initiatives that enhance community well-being from the comfort of your home. Our client is dedicated to improving healthcare outcomes through evidence-based practice and innovation. We offer a supportive and dynamic work environment, emphasizing professional growth and work-life balance. This role is notionally based in Sheffield, South Yorkshire, UK , but operates as a fully remote position. We are committed to creating an inclusive and diverse workforce.
Qualifications:
- Minimum of 5 years of experience in clinical research coordination or management.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials.
- Proven experience in managing multiple research projects simultaneously.
- Strong understanding of research methodologies, study design, and data management.
- Excellent leadership, communication, and interpersonal skills.
- Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Bachelor's degree in a relevant healthcare or life sciences field. A Master's degree or relevant professional certifications (e.g., CCRA) are highly desirable.
- Ability to work independently, exercise sound judgment, and make informed decisions.
- Strong organizational skills and attention to detail.
- Experience working effectively in a remote or distributed team environment.
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2
Senior Clinical Research Coordinator
OX1 1 Oxford, South East
£50000 Annually
WhatJobs
Posted 3 days ago
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Job Description
Our client, a leading global biopharmaceutical company, is seeking a dedicated and experienced Senior Clinical Research Coordinator to join their innovative team. This is a fully remote position, offering the opportunity to contribute to life-changing research from the comfort of your own home, whilst being integral to projects operating out of the **Oxford, Oxfordshire, UK** region. The successful candidate will play a crucial role in the successful execution of clinical trials, ensuring adherence to protocols, regulations, and high ethical standards. You will be responsible for managing various aspects of clinical trial operations, from patient recruitment and data management to site communication and regulatory compliance.
Key Responsibilities:
Key Responsibilities:
- Coordinate all operational aspects of assigned clinical trials, ensuring compliance with Good Clinical Practice (GCP) and other relevant regulations.
- Recruit, screen, and enroll eligible participants into clinical studies.
- Manage and maintain accurate and complete clinical trial documentation, including case report forms (CRFs) and source documents.
- Conduct patient visits, including vital signs, physical assessments, and administration of study medication/interventions as per protocol.
- Monitor study progress, track patient adherence, and report adverse events promptly.
- Liaise effectively with investigators, site staff, ethics committees, regulatory authorities, and sponsors.
- Prepare for and participate in site initiation, monitoring, and close-out visits.
- Contribute to the development and review of study-related documents, such as protocols and informed consent forms.
- Ensure the timely collection, management, and quality control of clinical data.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field; Master's degree is a plus.
- Minimum of 5 years of experience as a Clinical Research Coordinator or similar role in clinical trial management.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials.
- Experience with various clinical trial phases (Phase I-IV) is highly desirable.
- Proficiency in Electronic Data Capture (EDC) systems and clinical trial management systems (CTMS).
- Excellent organizational, time management, and problem-solving skills.
- Strong written and verbal communication abilities.
- Ability to work autonomously and effectively manage multiple priorities in a remote setting.
- A proactive and detail-oriented approach to work.
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3
Remote Clinical Research Coordinator
SW1A 0AA London, London
£35000 Annually
WhatJobs
Posted 3 days ago
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Job Description
Our client, a pioneering biotechnology firm dedicated to advancing medical research, is seeking a meticulous and dedicated Remote Clinical Research Coordinator. This fully remote role offers the opportunity to contribute to groundbreaking studies from the convenience of your home. You will be responsible for the day-to-day management of clinical trials, ensuring adherence to protocols, regulatory guidelines, and ethical standards. This position requires exceptional organisational skills, a keen eye for detail, and a strong understanding of clinical research processes. You will play a vital role in bringing life-changing therapies to patients.
Key Responsibilities:
Key Responsibilities:
- Coordinating all phases of clinical trials, from initiation to close-out, ensuring compliance with study protocols.
- Recruiting, screening, and consenting study participants according to eligibility criteria.
- Managing study documentation, including case report forms (CRFs), source documents, and regulatory binders.
- Administering study-related procedures and collecting data accurately and efficiently.
- Monitoring participant adherence to protocols and managing adverse event reporting.
- Liaising with investigators, site staff, sponsors, and regulatory authorities.
- Maintaining data integrity and ensuring timely data entry into electronic data capture (EDC) systems.
- Managing study supplies, equipment, and laboratory samples.
- Ensuring compliance with Good Clinical Practice (GCP) guidelines and all applicable regulations.
- Communicating effectively with participants and providing them with necessary information and support throughout the trial.
- Bachelor's degree in a life science, nursing, or a related field.
- Minimum of 2 years of experience in clinical research coordination.
- Proficiency in understanding and applying clinical trial protocols.
- Familiarity with GCP guidelines and regulatory requirements (e.g., ICH).
- Experience with electronic data capture (EDC) systems.
- Strong organisational and time management skills.
- Excellent attention to detail and accuracy in data collection and record-keeping.
- Effective communication and interpersonal skills, with the ability to interact professionally with participants and healthcare professionals.
- Ability to work independently and manage responsibilities effectively in a remote setting.
- Basic knowledge of medical terminology and disease processes relevant to ongoing research.
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4
Remote Clinical Research Coordinator
BS1 3DQ Bristol, South West
£38000 Annually
WhatJobs
Posted 3 days ago
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Job Description
Our client, a pioneering force in healthcare innovation, is seeking a dedicated and highly organized Remote Clinical Research Coordinator to join their fully remote operations team. This position is crucial for the successful execution of clinical trials, supporting research professionals and participants from anywhere in the UK. You will be responsible for a wide range of administrative and operational tasks essential to the smooth running of research studies. Your duties will include managing study documentation, maintaining accurate participant records, coordinating study visits (virtually and, when necessary, facilitating in-person arrangements with local sites), and liaising with investigators, site staff, and study sponsors. A deep understanding of Good Clinical Practice (GCP) guidelines and relevant regulatory requirements is essential. The ideal candidate will possess exceptional organizational skills, meticulous attention to detail, and the ability to manage multiple tasks simultaneously in a remote work environment. Strong communication and interpersonal skills are vital for effectively interacting with diverse stakeholders, including patients, healthcare professionals, and research teams via virtual platforms. You will play a key role in ensuring data integrity, participant safety, and trial adherence to protocol. Experience with electronic data capture (EDC) systems and clinical trial management software is highly desirable. This role requires a proactive approach, excellent problem-solving capabilities, and the ability to work independently with minimal supervision. You will contribute to groundbreaking research aimed at improving patient outcomes and advancing medical knowledge. Opportunities for professional growth within a dynamic and supportive remote team are extensive. If you are passionate about healthcare research and thrive in a flexible, remote-first setting, this is an exceptional opportunity.Bristol, South West England, UK is the administrative base, but this role is 100% remote.
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5
Senior Clinical Research Coordinator - Remote
NR2 1AX Norwich, Eastern
£55000 Annually
WhatJobs
Posted 2 days ago
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Job Description
Our client, a leading non-profit organization dedicated to advancing healthcare through research, is seeking a highly experienced Senior Clinical Research Coordinator to join their remote team. This role is vital in managing and coordinating complex clinical trials, ensuring adherence to protocols, regulatory requirements, and ethical standards. As a remote position, you will leverage your organizational skills and communication expertise to support research sites and study participants from your home office. This role demands a meticulous approach to data management, participant engagement, and regulatory compliance.
Responsibilities:
Responsibilities:
- Coordinate all aspects of clinical trial conduct at assigned research sites, ensuring compliance with study protocols, GCP, and regulatory guidelines.
- Manage participant recruitment, screening, enrollment, and follow-up according to study requirements.
- Oversee the collection, processing, and accurate documentation of study data, ensuring data integrity and completeness.
- Administer study medications and perform study-related procedures as delegated and trained.
- Manage investigational product accountability and ensure proper storage and handling.
- Liaise effectively with principal investigators, site staff, sponsors, and regulatory authorities.
- Prepare for and participate in site initiation visits, monitoring visits, and close-out visits.
- Maintain accurate and organized study documentation, including source documents and regulatory binders.
- Ensure the safety and well-being of study participants, reporting any adverse events promptly.
- Utilize remote communication tools and platforms to maintain effective collaboration with research sites and the central study team.
- Bachelor's degree in Nursing, Life Sciences, Allied Health, or a related field. A Master's degree is a plus.
- Minimum of 5 years of experience as a Clinical Research Coordinator in academic or industry settings.
- In-depth knowledge of Good Clinical Practice (GCP), ICH guidelines, and relevant regulatory requirements (e.g., FDA, MHRA).
- Experience with various clinical trial phases and therapeutic areas is desirable.
- Proficiency in electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Excellent organizational, time management, and problem-solving skills.
- Strong interpersonal and communication skills, with the ability to build rapport with participants and effectively collaborate with diverse teams remotely.
- Ability to work independently with minimal supervision and manage multiple priorities in a remote environment.
- Certification as a Certified Clinical Research Professional (CCRP) or equivalent is highly desirable.
- Proficiency in Microsoft Office Suite and other relevant software.
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6
Lead Clinical Research Coordinator (Remote)
PO1 1AA Portsmouth, South East
£50000 Annually
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Posted 3 days ago
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Job Description
Our client is seeking a highly organized and experienced Lead Clinical Research Coordinator to join their fully remote clinical operations team. This vital role will involve overseeing and managing multiple clinical research studies, ensuring compliance with all ethical standards, regulatory requirements, and protocol guidelines. You will lead a team of research coordinators, providing training, mentorship, and day-to-day guidance to ensure the successful execution of research activities. Responsibilities include participant recruitment and retention, informed consent processes, data collection and management, and adverse event reporting. You will serve as a key liaison between investigators, study sponsors, regulatory agencies, and study participants. Developing and implementing study protocols, managing study budgets, and ensuring the accurate and timely submission of study documentation are critical. The ideal candidate will have a Bachelor's degree in a life science, nursing, or a related field; a Master's degree is a plus. Extensive experience as a Clinical Research Coordinator is required, with demonstrated experience in a leadership or senior role. A strong understanding of Good Clinical Practice (GCP), ICH guidelines, and relevant regulatory frameworks (e.g., FDA, EMA) is essential. Excellent organizational, problem-solving, and communication skills are mandatory. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is required. The ability to manage multiple complex projects simultaneously in a remote setting, maintain meticulous records, and work effectively with diverse teams is crucial. Join a leading research organization that is dedicated to advancing medical treatments and offers a flexible, remote work environment with opportunities for professional growth.
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7
Senior Clinical Research Coordinator (Remote)
NR1 3EX Norwich, Eastern
£40000 Annually
WhatJobs
Posted 3 days ago
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Job Description
Our client, a leading organisation dedicated to advancing healthcare through cutting-edge research, is seeking a highly organised and experienced Senior Clinical Research Coordinator to join their fully remote operations team. This role is critical in ensuring the smooth and compliant execution of clinical trials, supporting the recruitment, monitoring, and data management of study participants.
You will be responsible for coordinating all aspects of clinical research studies, working closely with principal investigators, study nurses, and sponsors. Key duties include participant screening and recruitment, obtaining informed consent, managing study documentation, ensuring adherence to protocols and Good Clinical Practice (GCP) guidelines, and accurately collecting and entering data into electronic data capture (EDC) systems. You will also be involved in scheduling participant visits, liaising with laboratories and diagnostic facilities, and addressing any study-related queries from participants or healthcare professionals.
The ideal candidate will possess a strong understanding of clinical trial phases, regulatory requirements (e.g., MHRA, FDA), and ethical considerations in research. Excellent communication, organisational, and interpersonal skills are essential for effective remote collaboration with diverse teams and for building rapport with study participants. Proficiency with EDC systems, electronic trial master files (eTMFs), and other clinical research software is required. Experience in a senior capacity, mentoring junior staff or taking ownership of specific study aspects, would be highly advantageous. This is a fantastic opportunity for a dedicated professional to contribute to life-saving research from the comfort of their own home.
Key Responsibilities:
You will be responsible for coordinating all aspects of clinical research studies, working closely with principal investigators, study nurses, and sponsors. Key duties include participant screening and recruitment, obtaining informed consent, managing study documentation, ensuring adherence to protocols and Good Clinical Practice (GCP) guidelines, and accurately collecting and entering data into electronic data capture (EDC) systems. You will also be involved in scheduling participant visits, liaising with laboratories and diagnostic facilities, and addressing any study-related queries from participants or healthcare professionals.
The ideal candidate will possess a strong understanding of clinical trial phases, regulatory requirements (e.g., MHRA, FDA), and ethical considerations in research. Excellent communication, organisational, and interpersonal skills are essential for effective remote collaboration with diverse teams and for building rapport with study participants. Proficiency with EDC systems, electronic trial master files (eTMFs), and other clinical research software is required. Experience in a senior capacity, mentoring junior staff or taking ownership of specific study aspects, would be highly advantageous. This is a fantastic opportunity for a dedicated professional to contribute to life-saving research from the comfort of their own home.
Key Responsibilities:
- Coordinate the day-to-day operations of clinical research studies.
- Screen potential participants and obtain informed consent.
- Manage study-related data and documentation accurately.
- Ensure compliance with study protocols and regulatory guidelines (GCP).
- Schedule and coordinate participant appointments and study visits.
- Liaise with investigators, research staff, and sponsors.
- Maintain electronic trial master files (eTMF) and other essential documents.
- Assist with site initiation, monitoring, and close-out visits.
- Address participant queries and provide support throughout the study.
- Contribute to study planning and protocol development.
- Bachelor's degree in a relevant healthcare or scientific field (e.g., Nursing, Life Sciences).
- Minimum of 3-5 years' experience as a Clinical Research Coordinator.
- Demonstrable knowledge of clinical trial phases, GCP, and regulatory requirements.
- Proficiency with Electronic Data Capture (EDC) systems and eTMF.
- Excellent organisational, time management, and multitasking skills.
- Strong communication and interpersonal skills for remote team and participant interaction.
- Ability to work independently with minimal supervision.
- Attention to detail and commitment to data accuracy.
- Certification from a recognised professional body (e.g., ACRP, SoCRA) is desirable.
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8
Remote Clinical Research Coordinator - Specialist
LS1 1UR Leeds, Yorkshire and the Humber
£45000 Annually
WhatJobs
Posted 3 days ago
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Job Description
Our client, a pioneering biopharmaceutical company focused on developing innovative treatments for rare diseases, is seeking a dedicated and experienced Remote Clinical Research Coordinator (Specialist) to join their growing team. This position is fully remote, allowing you to contribute significantly to groundbreaking medical research from the comfort of your home office, anywhere in the UK. You will play a crucial role in the operational execution of clinical trials, ensuring adherence to protocols, regulatory guidelines, and the highest standards of patient safety and data integrity. Your expertise will be vital in managing study logistics, supporting site operations, and facilitating effective communication between study teams, investigators, and participants.
Responsibilities:
Responsibilities:
- Coordinate and manage all operational aspects of assigned clinical trials in accordance with study protocols, GCP, and relevant regulations.
- Ensure accurate and timely collection, documentation, and reporting of study data using electronic data capture (EDC) systems.
- Manage study supplies, including investigational products, and ensure proper storage and accountability.
- Screen, recruit, and enroll eligible participants into clinical trials, ensuring informed consent is obtained correctly.
- Monitor study progress, identify potential issues or deviations, and implement corrective actions.
- Maintain comprehensive study documentation, including regulatory binders, source documents, and case report forms.
- Liaise effectively with principal investigators, study site staff, and clinical research associates (CRAs).
- Facilitate communication and information flow between the study team, sponsors, and regulatory authorities.
- Assist with site initiation visits, interim monitoring visits, and close-out visits.
- Participate in study team meetings and contribute to protocol development and amendment processes.
- Ensure compliance with all ethical considerations and patient confidentiality requirements.
- Support data query resolution and contribute to final study reports.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field; Master's degree preferred.
- Minimum of 4 years of direct experience as a Clinical Research Coordinator or in a similar clinical research role.
- In-depth knowledge of Good Clinical Practice (GCP), ICH guidelines, and relevant regulatory requirements.
- Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Excellent organizational skills, with meticulous attention to detail.
- Strong communication, interpersonal, and problem-solving abilities.
- Ability to work independently, manage multiple priorities, and meet deadlines in a remote setting.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
- Experience in rare disease research is a significant advantage.
- Must be authorized to work remotely from within the United Kingdom.
This advertiser has chosen not to accept applicants from your region.
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