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ICON plc · Posted Nov 12, 2026
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Clinical Research Associate II responsible for monitoring clinical trials, ensuring protocol compliance, data integrity, and patient safety.
Conduct site qualification, initiation, monitoring, and close‑out visits Ensure protocol compliance and data integrity Collaborate with investigators and site staff Perform data review and query resolution Prepare and review study documentation Bachelor's degree in a scientific or healthcare-related field Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources ICON plc · Posted Nov 11, 2026
Design and analyse clinical trials, monitor sites, ensure protocol compliance, and manage data quality for clinical research studies.
Conduct site qualification, initiation, monitoring, and close‑out visits Ensure protocol compliance, data integrity, and patient safety Collaborate with investigators and site staff Perform data review and query resolution Prepare and review study documentation Bachelor's degree in a scientific or healthcare‑related field Competitive base salary Performance related incentives Health and wellbeing programmes Absa Group · Posted Dec 18, 2023
To build and maintain professional business relationships across a portfolio of Private Wealth clients, by achieving financial targets, proactively acquiring new clients, and improving customer experience within the scope of the Bank’s regulatory and compliance frameworks.
New Business Origination Manage and grow existing client relationships Involvement in credit related tasks Involvement in Assets under Management and Investments Stakeholder Management Bachelor's Degrees and Advanced Diplomas: Business, Commerce and Management Studies ICON plc · Posted Nov 10, 2026
Clinical Research Associate responsible for designing, analysing, and monitoring clinical trials.
Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials Ensure protocol compliance, data integrity, and patient safety throughout the trial process Collaborate with investigators and site staff to facilitate smooth study conduct Perform data review and resolve queries to maintain high-quality clinical data Contribute to the preparation and review of study documentation, including protocols and clinical study reports Bachelor's degree in a scientific or healthcare-related field ICON plc · Posted Nov 10, 2026
Clinical Research Associate responsible for monitoring and managing clinical trials, ensuring protocol compliance, data integrity, and patient safety.
Conduct site qualification, initiation, monitoring, and close‑out visits for clinical trials Ensure protocol compliance, data integrity, and patient safety throughout the trial process Collaborate with investigators and site staff to facilitate smooth study conduct Perform data review and resolution of queries to maintain high‑quality clinical data Contribute to the preparation and review of study documentation, including protocols and clinical study reports Bachelor's degree in a scientific or healthcare‑related field ICON plc · Posted Nov 10, 2026
Clinical Research Associate II responsible for monitoring clinical trials, ensuring protocol compliance, and managing data integrity.
Conduct site qualification, initiation, monitoring, and close‑out visits for clinical trials Ensure protocol compliance, data integrity, and patient safety throughout the trial process Collaborate with investigators and site staff to facilitate smooth study conduct Perform data review and resolution of queries to maintain high‑quality clinical data Contribute to the preparation and review of study documentation, including protocols and clinical study reports Bachelor's degree in a scientific or healthcare‑related field PSI CRO · Posted Nov 10, 2026
Senior CRA to manage the clinical aspects of full-service global projects in Taiwan.
Training, mentoring and supervising study level responsibilities for Junior CRAs Preparation, conduct, and reporting of selection, initiation, routine and closeout monitoring visits Delivering training of investigators, site staff and project teams Work with complex studies Perform CRF review, source document verification and query resolution College/University degree in Life Sciences or an equivalent combination of education, training & experience Nice to have: Inflammatory Bowel Disease Nice to have: Oncology Nice to have: Infectious Diseases Radius Limited · Posted Nov 10, 2026
As an Operations Assistant, you’ll look after an area of the Group’s operational processes, owning end-to-end processes for several products.
We also offer: Global Female Health Policy & Female Health Champions Pregnancy Loss and Fertility Treatment Policies Endometriosis Friendly Employer (UK) Women-focused gym & female health events Mental Health First Aiders Disability Confident Committed Employer (Level 2) Race at Work Charter signatory Proud sponsor of Crewe Pride (5 years running) and Cheshire Pride Awards Corporate Supporter 2025 Community network driving charity and volunteering initiatives, with 8 consecutive years of participation in the UK Challenge. Give as you earn scheme (payroll giving) and match funding
Process transactional data Validate high volumes of transactional data Deal with data issues that block invoicing Complete daily and weekly volume reconciliations and trend analysis Measure performance against internal service levels Bachelor's degree (minimum 2:2) Nice to have: Finance or operations role experience Nice to have: Transactional or billing data experience Core benefits Bonus potential Competitive compensation DM Clinical Research · Posted Nov 5, 2026
Coordinate and manage psychiatric clinical trials at assigned investigative sites, ensuring compliance with sponsor protocols, FDA regulations, and ICH/GCP guidelines.
Complete required training including ICH-GCP and IATA certifications Attend protocol and amendment trainings Conduct study subject visits and document procedures Enter data and resolve queries Follow up on action items High School Diploma or equivalent Bachelor's degree in Psychology, Neuroscience, Biology, Public Health, Nursing, or related health science discipline Nice to have: Bilingual English/Spanish Nice to have: ACRP certification Syngene International Limited · Posted Nov 4, 2026
Independently perform and coordinate clinical data management activities for assigned clinical studies, ensuring accurate, complete, consistent, and GCP/regulatory‑compliant clinical trial data.
Execute assigned clinical data management activities in accordance with study requirements, timelines, SOPs, and regulatory guidelines. Perform data review, validation, and cleaning activities to ensure data accuracy, completeness, and consistency. Raise, track, and facilitate timely resolution of data queries with investigative sites and internal stakeholders. Monitor CRF/eCRF completion, query status, and data discrepancies to support study milestones. Support CRF/eCRF review, database testing, and User Acceptance Testing (UAT) activities as assigned. Bachelor's or Master's degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, Health Sciences, or a related discipline
Medical, dental and vision coverage
Retirement and pension plans
Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources
Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources
Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources
Development and learning opportunities Chance to make a real impact in a meaningful industry
Clinical Data ManagerSyngene International Limited · Bangalore, India