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Pertemps Cardiff
Neath
We are looking for an experienced Environmental Monitoring Assistant for an immediate start ongoing temporary assignment based in Swansea.Working within the Environmental Assessment and Advice Team you will assist in providing environmental monitoring, assessment advice and reporting, for the fisheries monitoring and sampling disciplines.This role
Job Source: Pertemps CardiffSecurity Cleared Jobs
United Kingdom, Swansea, Swansea (Abertawe), United Kingdom
Location: Swansea area with travel Salary: £24,102 per annum, Company Car Hours: 37.5hrs pw (Evenings - 5pm to 1pm on a shift/rota basis) Working as a Field Officer for our Electronic Monitoring Service is more than just a job, it's the chance to be a part of something great, to join a team where your contributions are valued, and where you can
Job Source: Security Cleared JobsLabour Tech Recruitment Ltd
Swansea, Wales, United Kingdom
We are thrilled to offer an outstanding opportunity for a Study Monitor to join our client’s dynamic team at their Factory site in Swansea. In this role, you will conduct routine site visits, assessing study progress, and fostering collaboration between Principal Investigators and research personnel. Additionally, you will oversee routine close-out
Job Source: Labour Tech Recruitment LtdLabour Tech Recruitment Ltd
Swansea
Job Description We are thrilled to offer an outstanding opportunity for a Study Monitor to join our client’s dynamic team at their Factory site in Swansea. In this role, you will conduct routine site visits, assessing study progress, and fostering collaboration between Principal Investigators and research personnel. Additionally, you will oversee
Job Source: Labour Tech Recruitment Ltdyolk recruitment
Swansea
Clinical Trials Manager £45,000 Swansea Hybrid working Yolk Recruitment has a new opportunity for a Clinical Trials Manager to join an expanding manufacturer who are leading competitors within the Medical Sector. This role reports directly to the Director of Clinical Affairs and is an opportunity for an established Clinical Trials Manager to j
Job Source: yolk recruitmentYolk Recruitment Ltd
Swansea
Clinical Trials Manager £45,000 Swansea Hybrid working Yolk Recruitment has a new opportunity for a Clinical Trials Manager to join an expanding manufacturer who are leading competitors within the Medical Sector. This role reports directly to the Director of Clinical Affairs and is an opportunity for an established Clinical Trials Manager to join a
Job Source: Yolk Recruitment LtdSmart Workforce Solutions
Swansea, Wales, United Kingdom
Smart Solutions are working with an award winning manufacturer based in Swansea. We are seeking for an enthusiastic experienced Clinical Trials Manager to join our Clinical and Application Research department. You will be responsible for all aspects of clinical trial management. The post holder will have a significant level of responsibility. Dut
Job Source: Smart Workforce SolutionsThe Recruitment Co
Swansea
The Recruitment Co are recruiting for an experienced Clinical Trials Manager to join our clients expanding team. A world-leading manufacturer of high-quality technical products. Contract: Permanent Salary: £45,000pa Shifts: Full time The Role: Responsible for all aspects of clinical trial management. The post holder will have a significant level
Job Source: The Recruitment CoSwansea
The Recruitment Co are recruiting for a Study Monitor (Clinical Operations) to join our clients expanding team. A world-leading manufacturer of high-quality technical products.
Contract: Permanent
Salary: £28,017pa
Shifts: Full time
The Role: Oversee the progress of clinical and application research/trials. To ensure all research is conducted, recorded, and reported in accordance with Protocols, SOPs, ICH-GCP and applicable regulatory requirements. Provide a global evaluation of all investigations commissioned and executed. The successful post holder will provide assistance in preparing study documentation for trials, IRB/IEC submissions and documentation for regulatory dossiers.
Solely responsible for ensuring collection of the required essential documents for study start-up and throughout the conduct of a trial. You will conduct on-site training and motivate the investigators. As part of document review, you will ensure accurate data is recorded across multiple investigations and verify patient data. You will ensure adherence to protocol, GCP and internal SOPs. You will maintain all files pertaining to the clinical trials, track study progress and ensure timely quality updates are provided.
Your responsibilities will include routine site visits and assessments. Your role will be to ensure all projects run optimally, and work is completed correctly and within designated timelines. You will bridge the gap between the Principal Investigator and research personnel, providing vital advice and making informed decisions. You will ensure Routine Close-out activities are completed and audit all activities undertaken at each investigative site.
Essential Requirements:
Solid degree in scientific subject
Experience in a clinical research setting; proven clinical trial experience.
Experience in Phase I-IV trials; Phase II - III is preferred.
Working knowledge of EU Clinical Trials Directive, Medical Device Directive, UK Clinical Trials Regulations, Principles of ICH-GCP, GDPR and Research Governance Framework Legislation with proven ability to apply these to the coordination of clinical trials.
Understanding of current EU Medical Device Regulation
Working knowledge of BS EN ISO 14155 is preferred.
Experience working effectively in a team/matrix environment.
Proven ability to manage multiple priorities and communicate effectively.
Key Objectives/KPIs
Motivate research team.
QA/QC investigators daily activities; ensuring compliance with CIP and regulatory compliance.
Ensure research staff achieve targets and deliverables in a timely manner.
Conduct detailed audits and trend analysis on key elements of trial execution; bridge the gap.
Procure, store, and disseminate study supplies (dispensing and accountability), including investigational devices.
Induct, train and mentor new department personnel, including competency testing.
Identify and devise new training materials as deemed appropriate.
Identify and devise new departmental SOPs/WI and template documentation, as deemed appropriate
If you have the required skills and experience required for this role then please submit your CV for immediate response.
CPSwansea
The Recruitment Co. is an equal opportunities employer and we're committed to diversity and inclusion in the workplace.
Study Monitor Clinical Operations jobs in Swansea
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