{"data":{"company":{"name":"Illingworth Research 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experienced Per Diem Pediatric/Adolescent Research Nurse to join our team in Hudsonville, Michigan.</p>\n<p>Illingworth Research Group is a global organisation operating in over 45 countries, bringing clinical research directly into the home of the patient, to improve the experience of patients involved in clinical trials and the quality of their lives.</p>\n<p><strong>Job Responsibilities</strong> As a Pediatric/Adolescent Research Nurse, you will be responsible for:</p>\n<ul>\n<li>Conducting clinical research studies in the patient&#39;s home</li>\n<li>Providing high-quality care to pediatric and adolescent patients</li>\n<li>Collecting and recording data accurately</li>\n<li>Communicating effectively with patients, families, and healthcare professionals</li>\n<li>Working independently and as part of a wider team</li>\n</ul>\n<p><strong>Qualifications</strong> To be considered for this role, you will need:</p>\n<ul>\n<li>To be an experienced Registered Nurse (Pediatric/Adolescent)</li>\n<li>Experience and knowledge of working in clinical research trials with ICH-GCP (Good Clinical Practice) Certification (training can be provided)</li>\n<li>Attention to detail and highly organised</li>\n<li>Ability to prioritise and manage multiple tasks</li>\n<li>Excellent verbal and written communication skills in English</li>\n<li>Good IT skills and a working knowledge of computer software</li>\n<li>Trained in Handling and Transport of Hazardous Substances (preferable, training can be provided)</li>\n<li>Clinical skills in areas such as phlebotomy, subcutaneous injections, ECGs, and cannulation</li>\n</ul>\n<p><strong>Benefits</strong></p>\n<ul>\n<li>Competitive pay rates $47-57 per hour</li>\n<li>Hourly rate paid for travel time as well as time spent with the patient in their home</li>\n<li>Mileage reimbursement</li>\n<li>Flexible working shifts</li>\n<li>Project-specific training provided</li>\n<li>Ongoing training and line management support</li>\n</ul>\n<p><strong>Additional Information</strong></p>\n<ul>\n<li>A driving license and access to a vehicle are essential for this role</li>\n<li>You will be required to travel</li>\n</ul>","enriched_at":1793315990252},{"id":"job_23191303-3cb","title":"Part Time Research Nurse","source_url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/ESP-Remote-Madrid/Part-Time-Research-Nurse---Santiago-De-Compostela_25113226","location":"Santiago De Compostela","job_type":"part-time","experience_level":"senior","work_arrangement":null,"category":"Healthcare","description":"<p>We are seeking a Part Time Research Nurse to join our team in Santiago De Compostela.</p>\n<p>Illingworth Research Group is a global organisation operating in over 45 countries, bringing clinical research directly into the home of the patient, to improve the experience of patients involved in clinical trials and the quality of their lives.</p>\n<p><strong>Job Responsibilities</strong></p>\n<ul>\n<li>Be fully conversant with the trial protocol, Case Report Forms (CRFs/eCRF), off-site manual (if applicable), supporting documents, procedures, and timelines to enable day-to-day running of the trial, including all relevant SOPs.</li>\n<li>Communicate effectively with the Illingworth research nurse project manager (RNPM), Research nurse manager, site staff, and the Principal Investigator, to ensure a smooth and efficient flow of information.</li>\n<li>Maintain accurate documentation, including electronic transfer of data as per Illingworth SOPs throughout the trial, ensuring subject confidentiality, adhering to GCP and data protection requirements.</li>\n<li>Attend Site Initiation Visits (SIV) as required and any other necessary meetings, including multi-disciplinary, project management, and client-facing meetings.</li>\n<li>Coordinate (working with the RN team) and complete subject trial visits on- and off-site. Ensure all trial-related procedures and assessments are completed according to the protocol and relevant SOPs and that data is collected accurately.</li>\n<li>Administer trial medication as per the protocol, and facilitate the safe storage, transfer, and accountability of trial medication in accordance with Illingworth SOPs.</li>\n<li>Process and safely package and dispatch samples, liaising with courier companies and organisations in line with project requirements and supporting documents.</li>\n<li>Assist in identifying potentially eligible patients for research projects and assist with patient recruitment into clinical trials, providing information and support for those patients for on- and off-site care.</li>\n<li>Ensure the accurate reporting of adverse events (AEs) and serious adverse events (SAEs)/suspected unexpected serious adverse reactions (SUSARs) to the site team and relevant RNPM, providing support for any additional follow-up that may be required.</li>\n<li>Report any suspected misconduct or fraud to Illingworth and associated companies.</li>\n</ul>\n<p><strong>Qualifications</strong></p>\n<ul>\n<li>Registered nurse with a minimum of 2 years&#39; post-qualification experience.</li>\n<li>Research and clinical trials experience with GCP certification.</li>\n<li>Knowledge of research design and methodology desirable.</li>\n<li>Experience and knowledge of clinical nursing skills such as Venepuncture and ECG preferable.</li>\n<li>Ability to work autonomously with initiative in a team within a multidisciplinary environment.</li>\n<li>Excellent verbal and written communication skills.</li>\n<li>Ability to prioritise and manage multiple tasks.</li>\n<li>Good working knowledge of computer software including Outlook, Word, Excel, and PowerPoint as a minimum.</li>\n</ul>","enriched_at":1793306946884},{"id":"job_3cdcfc1a-289","title":"Per Diem Freelance Research Nurse Pool","source_url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/FRA-Remote/Per-Diem-Freelance-Research-Nurse-Pool---Stay-Connected-with-us_25101890","location":"FRA-Remote","job_type":"contract","experience_level":"senior","work_arrangement":null,"category":"Healthcare","description":"<p>We are seeking a Per Diem Freelance Research Nurse Pool to support patients participating in clinical research studies. As a Research Nurse, you will play a crucial role in coordinating care and facilitating communication with healthcare providers.</p>\n<p><strong>Job Responsibilities</strong></p>\n<ul>\n<li>Support patients participating in clinical research studies by coordinating care and facilitating communication with healthcare providers</li>\n<li>Help patients understand study protocols, schedule appointments, and address concerns related to their participation</li>\n<li>Collaborate with research teams to monitor patient progress and collect data while ensuring compliance with regulatory standards</li>\n<li>Serve as a resource to help patients navigate the healthcare system and access necessary services throughout their research experience</li>\n<li>Ensure that participants remain engaged and compliant with study protocols to maintain the integrity and validity of the research</li>\n<li>Contribute to the overall efficiency and effectiveness of the research process by coordinating care and facilitating communication between patients and healthcare providers</li>\n<li>Ensure that patient data is accurately collected and monitored to enhance the quality of the research outcomes</li>\n<li>May be responsible for entire projects or processes within their area of responsibility, contributing to the design, implementation, and delivery of processes, programs, and policies</li>\n</ul>\n<p><strong>Qualifications</strong></p>\n<ul>\n<li>Bachelor&#39;s degree in Nursing or a related field</li>\n<li>Minimum of 3 years of experience in clinical research or patient care</li>\n<li>Strong understanding of clinical research protocols and regulatory standards</li>\n<li>Excellent communication and interpersonal skills</li>\n<li>Ability to work independently and as part of a team</li>\n</ul>\n<p><strong>Certifications</strong></p>\n<ul>\n<li>Registered Nurse (RN) license or equivalent work France Specific</li>\n<li>Certification in Clinical Research (e.g., CCRP, CCRC) preferred</li>\n</ul>\n<p><strong>Necessary Skills</strong></p>\n<ul>\n<li>In-depth knowledge and skills within the professional discipline of clinical research and patient care</li>\n<li>Ability to coordinate care and facilitate communication between patients and healthcare providers</li>\n<li>Strong organizational and time management skills</li>\n<li>Ability to address patient concerns and provide individualized support</li>\n<li>Proficiency in data collection and monitoring</li>\n<li>Understanding of the impact of work on related areas and the ability to manage processes and programs</li>\n</ul>","enriched_at":1793167705911},{"id":"job_ce6e1b5c-47a","title":"Research Nurse - Danbury, Connecticut (Per Diem)","source_url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/USA-CT-Remote/Research-Nurse---Danbury--Connecticut--Per-Diem-_25111267","location":"Danbury, Connecticut","job_type":"temporary","experience_level":"senior","work_arrangement":null,"category":"Healthcare","description":"<p>We are seeking a Research Nurse to join our team in Danbury, Connecticut. As a Research Nurse with Illingworth Research Group, you will play a crucial role in delivering high-quality clinical research services directly to patients in their homes.</p>\n<p><strong>Job Responsibilities:</strong></p>\n<ul>\n<li>Be fully conversant with the trial protocol, Case Report Forms (CRFs/eCRF), off-site manual, supporting documents, procedures, and timelines to enable day-to-day running of the trial, including all relevant SOPs.</li>\n<li>Communicate effectively with the Illingworth research nurse project manager (RNPM), Research nurse manager, site staff, and the Principal Investigator to ensure a smooth and efficient flow of information.</li>\n<li>Maintain accurate documentation, including electronic transfer of data as per Illingworth SOPs throughout the trial, ensuring subject confidentiality, adhering to GCP and data protection requirements.</li>\n<li>Attend Site Initiation Visits (SIV) as required and any other necessary meetings, including multi-disciplinary, project management, and client-facing meetings.</li>\n<li>Coordinate and complete subject trial visits on- and off-site, ensuring all trial-related procedures and assessments are completed according to the protocol and relevant SOPs, and that data is collected accurately.</li>\n<li>Administer trial medication as per the protocol and facilitate the safe storage, transfer, and accountability of trial medication in accordance with Illingworth SOPs.</li>\n<li>Process and safely package and dispatch samples, liaising with courier companies and organizations in line with project requirements and supporting documents.</li>\n<li>Assist in identifying potentially eligible patients for research projects and assist with patient recruitment into clinical trials, providing information and support for those patients for on- and off-site care.</li>\n<li>Ensure the accurate reporting of adverse events (AEs) and serious adverse events (SAEs)/suspected unexpected serious adverse reactions (SUSARs) to the site team and relevant RNPM, providing support for any additional follow-up that may be required.</li>\n<li>Report any suspected misconduct or fraud to Illingworth and associated companies.</li>\n</ul>\n<p><strong>Qualifications:</strong></p>\n<ul>\n<li>Registered nurse with a minimum of 2 years&#39; post-qualification experience.</li>\n<li>Research and clinical trials experience with GCP certification.</li>\n<li>Knowledge of research design and methodology desirable.</li>\n<li>Experience and knowledge of clinical nursing skills such as Venepuncture and ECG preferable.</li>\n<li>Ability to work autonomously with initiative in a team within a multidisciplinary environment.</li>\n<li>Excellent verbal and written communication skills.</li>\n<li>Ability to prioritize and manage multiple tasks.</li>\n<li>Good working knowledge of computer software including Outlook, Word, Excel, and PowerPoint as a minimum.</li>\n</ul>\n<p><strong>Benefits:</strong></p>\n<ul>\n<li>Hourly rate: $43-53 per hour</li>\n<li>Per diem (as needed role)</li>\n<li>Additional benefits may include a company car or car allowance, health benefits, company match 401k, eligibility to participate in Employee Stock Purchase Plan, eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time.</li>\n</ul>\n<p><strong>Salary Range:</strong></p>\n<p>$67,700.00 - $115,100.00</p>","enriched_at":1793157911405},{"id":"job_11733318-5de","title":"Research Nurse (Per Diem)","source_url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/USA-IN-Remote/Research-Nurse--Per-Diem----Fort-Wayne--IN_25113016","location":"Fort Wayne, Seymour, Indianapolis, IN","job_type":"temporary","experience_level":"senior","work_arrangement":null,"category":"Healthcare","description":"<p>We are seeking a Research Nurse (Per Diem) to join our team at Illingworth Research Group, a global organisation operating in over 45 countries, providing clinical research services directly to patients&#39; homes.</p>\n<p>The successful candidate will be fully conversant with the trial protocol, Case Report Forms (CRFs/eCRF), and supporting documents to enable the day-to-day running of the trial.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Communicating effectively with the Research Nurse Project Manager, Research Nurse Manager, site staff, and the Principal Investigator</li>\n<li>Maintaining accurate documentation, including electronic transfer of data</li>\n<li>Attending Site Initiation Visits (SIV) and other necessary meetings</li>\n<li>Coordinating and completing subject trial visits on- and off-site</li>\n<li>Administering trial medication and facilitating its safe storage and transfer</li>\n<li>Processing and dispatching samples</li>\n<li>Assisting in identifying potentially eligible patients and supporting patient recruitment</li>\n<li>Ensuring accurate reporting of adverse events</li>\n<li>Reporting any suspected misconduct or fraud</li>\n</ul>\n<p>Requirements:</p>\n<ul>\n<li>Registered nurse with a minimum of 2 years&#39; post-qualification experience</li>\n<li>Research and clinical trials experience with GCP certification</li>\n<li>Knowledge of research design and methodology desirable</li>\n<li>Experience and knowledge of clinical nursing skills such as Venepuncture and ECG preferable</li>\n<li>Ability to work autonomously with initiative in a team</li>\n<li>Excellent verbal and written communication skills</li>\n<li>Ability to prioritize and manage multiple tasks</li>\n<li>Good working knowledge of computer software, including Outlook, Word, Excel, and PowerPoint</li>\n</ul>\n<p>Benefits may include a company car or car allowance, health benefits, company match 401k, eligibility to participate in Employee Stock Purchase Plan, eligibility to earn commissions/bonus, and flexible paid time off (PTO) and sick time.</p>\n<p>Salary Range: $67,700.00 - $115,100.00</p>","enriched_at":1793140777015},{"id":"job_4b2e98a5-7de","title":"Site Augmentation Lead","source_url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/SRB-Remote/Site-Augmentation-Lead_25111815","location":"SRB-Remote","job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"Healthcare","description":"<p>Illingworth Research Group is seeking a Site Augmentation Lead. The successful candidate will be the primary point of contact for sponsor clients, sites, and Illingworth business units for site solutions projects.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Oversee and manage site solutions projects, ensuring they are delivered on time, within budget, and to the required quality standards</li>\n<li>Liaise with clients, sites, and internal stakeholders to resolve issues and ensure project success</li>\n<li>Develop and implement project plans, budgets, and resource allocation strategies</li>\n<li>Manage project finances, including budgeting, forecasting, and invoicing</li>\n<li>Ensure compliance with relevant regulations, SOPs, and GCP guidelines</li>\n<li>Build and maintain strong relationships with site stakeholders and sponsors</li>\n<li>Provide input to corrective and preventive actions related to quality issues</li>\n<li>Support the development of site relationships and future horizon planning for site solutions and optimization strategies</li>\n<li>Collaborate with study teams to define and lead site engagement and contracting processes</li>\n<li>Lead site solutions-related resource management, including requesting site-level resources and communicating changes to resource requirements</li>\n<li>Act as a company champion for site and sponsor clients</li>\n<li>Support the delivery and implementation of site solutions initiatives</li>\n</ul>\n<p>Additional Information: The company reserves the right to assign other tasks, duties, and responsibilities. Equivalent experience, skills, and/or education will be considered.</p>","enriched_at":1793140473768},{"id":"job_780d951e-13e","title":"Site Augmentation Lead","source_url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/BRA-Remote/Site-Augmentation-Lead_25111809","location":"BRA-Remote","job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"Healthcare","description":"<p>Illingworth Research Group is seeking a Site Augmentation Lead. The successful candidate will be responsible for overseeing site augmentation projects, ensuring they are delivered on time, within budget, and to the required quality standards.</p>\n<p><strong>Key Responsibilities:</strong></p>\n<ul>\n<li>Be the primary point of contact for sponsor clients, sites, and Illingworth business units for allocated site augmentation projects</li>\n<li>Oversee day-to-day project activities, ensuring compliance with clinical SOPs, GCP, and regulatory requirements</li>\n<li>Develop and manage project budgets, forecasts, and financial reporting</li>\n<li>Lead the development of project-related documentation, ensuring compliance with policies, SOPs, and regulatory requirements</li>\n<li>Deliver site augmentation projects through effective communication, implementation plans, and performance metrics</li>\n<li>Build and maintain relationships with sites, sponsors, and Illingworth business units</li>\n<li>Ensure that project deliverables meet customer expectations, including contracted deliverables, projections, reports, and updates</li>\n<li>Identify changes in scope and seek client approval for change orders</li>\n<li>Provide input to corrective and preventive action associated with quality issue resolution</li>\n<li>Collaborate with study teams to define and lead site engagement and contracting processes</li>\n<li>Support the development of collaborative and effective site relationships and future horizon planning for site solutions and optimization strategies</li>\n</ul>\n<p><strong>Additional Requirements:</strong></p>\n<ul>\n<li>Ability to understand and translate protocol requirements to deliver proposed site solutions</li>\n<li>Experience in managing site augmentation projects and teams</li>\n<li>Strong communication and leadership skills</li>\n</ul>","enriched_at":1793140459742},{"id":"job_7a50c156-e5e","title":"Per Diem Freelance Research Nurse","source_url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/FRA-Remote/Per-Diem-Freelance-Research-Nurse---Nice--France-_25105227","location":"Nice","job_type":"contract","experience_level":"senior","work_arrangement":"onsite","category":"Healthcare","description":"<p>We are seeking a Per Diem Freelance Research Nurse to join our team in Nice, France.</p>\n<p>Illingworth Research Group is a global organisation operating in over 45 countries, bringing clinical research directly into the home of the patient, to improve the experience of patients involved in clinical trials and the quality of their lives.</p>\n<p><strong>Job Responsibilities</strong></p>\n<ul>\n<li>Be fully conversant with the trial protocol, Case Report Forms (CRFs/eCRF), off-site manual, supporting documents, procedures, and timelines to enable day-to-day running of the trial, including all relevant SOPs.</li>\n<li>Communicate effectively with the Illingworth research nurse project manager (RNPM), Research nurse manager, site staff, and the Principal Investigator, to ensure a smooth and efficient flow of information.</li>\n<li>Maintain accurate documentation, including electronic transfer of data as per Illingworth SOPs throughout the trial, ensuring subject confidentiality, adhering to GCP and data protection requirements.</li>\n<li>Attend Site Initiation Visits (SIV) as required and any other necessary meetings, including multi-disciplinary, project management, and client-facing meetings.</li>\n<li>Coordinate and complete subject trial visits on- and off-site, working with the RN team.</li>\n<li>Administer trial medication as per the protocol, and facilitate the safe storage, transfer, and accountability of trial medication in accordance with Illingworth SOPs.</li>\n<li>Process and safely package and dispatch samples, liaising with courier companies and organisations in line with project requirements and supporting documents.</li>\n<li>Assist in identifying potentially eligible patients for research projects and assist with patient recruitment into clinical trials, providing information and support for those patients for on- and off-site care.</li>\n<li>Ensure accurate reporting of adverse events (AEs) and serious adverse events (SAEs)/suspected unexpected serious adverse reactions (SUSARs) to the site team and relevant RNPM.</li>\n<li>Report any suspected misconduct or fraud to Illingworth and associated companies.</li>\n</ul>\n<p><strong>Qualifications</strong></p>\n<ul>\n<li>Registered nurse with a minimum of 2 years&#39; post-qualification experience.</li>\n<li>Research and clinical trials experience with GCP certification.</li>\n<li>Knowledge of research design and methodology desirable.</li>\n<li>Experience and knowledge of clinical nursing skills such as venepuncture and ECG preferable.</li>\n<li>Ability to work autonomously with initiative in a team within a multi-disciplinary environment.</li>\n<li>Excellent verbal and written communication skills.</li>\n<li>Ability to prioritise and manage multiple tasks.</li>\n<li>Good working knowledge of computer software, including Outlook, Word, Excel, and PowerPoint as a minimum.</li>\n</ul>","enriched_at":1793134992183},{"id":"job_8d986b1e-801","title":"Research Nurse - Per Diem - Independent Contractor","source_url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/CAN-Remote/Research-Nurse---Per-Diem---Independent-Contractor---Vernon--British-Columbia_25111590","location":"Vernon, British Columbia","job_type":"contract","experience_level":"senior","work_arrangement":null,"category":"Healthcare","description":"<p>We are seeking a Research Nurse to join our team on a per diem basis as an independent contractor. As a Research Nurse with Illingworth Research Group, you will play a crucial role in delivering high-quality clinical research services directly to patients in their homes.</p>\n<p><strong>Job Responsibilities</strong></p>\n<ul>\n<li>Be fully conversant with the trial protocol, Case Report Forms (CRFs/eCRF), off-site manual, supporting documents, procedures, and timelines to enable the day-to-day running of the trial, including all relevant SOPs.</li>\n<li>Communicate effectively with the Illingworth research nurse project manager (RNPM), Research nurse manager, site staff, and the Principal Investigator to ensure a smooth and efficient flow of information.</li>\n<li>Maintain accurate documentation, including electronic transfer of data as per Illingworth SOPs throughout the trial, ensuring subject confidentiality, adhering to GCP and data protection requirements.</li>\n<li>Attend Site Initiation Visits (SIV) as required and any other necessary meetings, including multi-disciplinary, project management, and client-facing meetings.</li>\n<li>Coordinate and complete subject trial visits on- and off-site, working with the RN team to ensure all trial-related procedures and assessments are completed according to the protocol and relevant SOPs, and that data is collected accurately.</li>\n<li>Administer trial medication as per the protocol and facilitate the safe storage, transfer, and accountability of trial medication in accordance with Illingworth SOPs.</li>\n<li>Process and safely package and dispatch samples, liaising with courier companies and organizations in line with project requirements and supporting documents.</li>\n<li>Assist in identifying potentially eligible patients for research projects and assist with patient recruitment into clinical trials, providing information and support for those patients for on- and off-site care.</li>\n<li>Ensure the accurate reporting of adverse events (AEs) and serious adverse events (SAEs)/suspected unexpected serious adverse reactions (SUSARs) to the site team and relevant RNPM, providing support for any additional follow-up that may be required.</li>\n<li>Report any suspected misconduct or fraud to Illingworth and associated companies.</li>\n</ul>\n<p><strong>Qualifications</strong></p>\n<ul>\n<li>Registered nurse with a minimum of 2 years&#39; post-qualification experience.</li>\n<li>Research and clinical trials experience with GCP certification.</li>\n<li>Knowledge of research design and methodology desirable.</li>\n<li>Experience and knowledge of clinical nursing skills such as venepuncture and ECG preferable.</li>\n<li>Ability to work autonomously with initiative in a team within a multidisciplinary environment.</li>\n<li>Excellent verbal and written communication skills.</li>\n<li>Ability to prioritize and manage multiple tasks.</li>\n<li>Good working knowledge of computer software including Outlook, Word, Excel, and PowerPoint as a minimum.</li>\n</ul>","enriched_at":1793131152915},{"id":"job_14d68a21-2cf","title":"Adult Research Nurse - Crete","source_url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/GRC-Remote/Adult-Research-Nurse---Crete_25112450","location":"GRC-Remote","job_type":null,"experience_level":"senior","work_arrangement":null,"category":"Healthcare","description":"<p>We are seeking an Adult Research Nurse to join our team in Crete. As an Adult Research Nurse, you will play a crucial role in delivering high-quality clinical research services to patients.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Be fully conversant with the trial protocol, Case Report Forms (CRFs/eCRF), off-site manual, supporting documents, procedures, and timelines to enable day-to-day running of the trial.</li>\n<li>Communicate effectively with the Illingworth research nurse project manager, Research nurse manager, site staff, and the Principal Investigator to ensure a smooth flow of information.</li>\n<li>Maintain accurate documentation, including electronic transfer of data, and ensure subject confidentiality, adhering to GCP and data protection requirements.</li>\n<li>Attend Site Initiation Visits (SIV) and other necessary meetings, including multi-disciplinary, project management, and client-facing meetings.</li>\n<li>Coordinate and complete subject trial visits on- and off-site, ensuring all trial-related procedures and assessments are completed according to the protocol and relevant SOPs.</li>\n<li>Administer trial medication as per the protocol and facilitate the safe storage, transfer, and accountability of trial medication.</li>\n<li>Process and safely package and dispatch samples, liaising with courier companies and organizations as needed.</li>\n<li>Assist in identifying potentially eligible patients for research projects and assist with patient recruitment into clinical trials.</li>\n<li>Ensure accurate reporting of adverse events and serious adverse events to the site team and relevant RNPM.</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Registered nurse with a minimum of 2 years&#39; post-qualification experience.</li>\n<li>Research and clinical trials experience with GCP certification.</li>\n<li>Knowledge of research design and methodology desirable.</li>\n<li>Experience and knowledge of clinical nursing skills such as venepuncture and ECG preferable.</li>\n<li>Ability to work autonomously with initiative in a team within a multidisciplinary environment.</li>\n<li>Excellent verbal and written communication skills.</li>\n<li>Ability to prioritize and manage multiple tasks.</li>\n<li>Good working knowledge of computer software, including Outlook, Word, Excel, and PowerPoint.</li>\n</ul>\n<p>Additional Information:</p>\n<p>The tasks, duties, and responsibilities listed in this job description are not exhaustive. The Company reserves the right to assign other tasks, duties, and job responsibilities at its sole discretion.</p>","enriched_at":1792988935073}],"category_normalised":[{"category":"healthcare","count":10}],"velocity":{"weeks":[{"week_start":"2026-10-19","count":1},{"week_start":"2026-10-26","count":9}],"trend":"stable","wow_pct":800},"momentum":{"recent_14d":10,"prior_14d":0,"growth_pct":0,"classification":"stable"},"salary_vs_industry":{"company_median":91400,"industry_median":null,"percentile":null,"sample_size":2,"by_region":[],"transparency_pct":20,"industry_transparency_pct":0,"transparency_warning":false},"market_share":{"company_jobs":10,"industry_total":10,"share_pct":100,"rank":1,"peer_count":1},"ai_exposure":null,"peer_set":[],"skills_lq":[],"geographic_shift":{"current":[{"region":"Unknown","count":9,"share_pct":90},{"region":"United States","count":1,"share_pct":10}],"emerging":[{"region":"Unknown","recent_30d":9,"prior_30d":0,"growth_pct":100}],"shrinking":[]},"seniority_anomalies":{"exec_recent_30d":0,"exec_prior_90d_avg":0,"exec_growth_pct":0,"notable_exec_hires":[]},"posting_dynamics":{"median_days_open":null,"industry_median_days_open":null,"long_open_count":0,"closure_rate_pct":9}}}}