Study Monitor

3 months ago

Swansea, United Kingdom The Recruitment Co. Full time


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

  • Study Monitor

    3 days ago

    Swansea, City and County of Swansea, United Kingdom Cyden Ltd Full time

    Job Title: Study MonitorWe are seeking a highly skilled Study Monitor to join our Clinical and Application Research Team at Cyden Ltd. The successful candidate will be responsible for overseeing the progress of clinical and application research/trials, ensuring all research is conducted, recorded, and reported in accordance with Protocols, SOPs, ICH-GCP, and...

  • Study Monitor

    3 days ago

    Swansea, City and County of Swansea, United Kingdom Cyden Ltd Full time

    Job Title: Study MonitorWe are seeking a highly skilled Study Monitor to join our Clinical and Application Research Team at Cyden Ltd. The successful candidate will be responsible for overseeing the progress of clinical and application research/trials, ensuring all research is conducted, recorded, and reported in accordance with Protocols, SOPs, ICH-GCP, and...

  • Study Monitor

    7 days ago

    Swansea, City and County of Swansea, United Kingdom The Recruitment Co. Full time

    The Recruitment Company is seeking a dedicated Study Monitor for Clinical Operations to join a dynamic team within a prestigious technical products manufacturer. This permanent position offers a competitive salary of £28,017 per annum, with full-time shifts. Key Responsibilities: * Monitor and oversee progress of clinical and application research/trials *...

  • Study Monitor

    6 days ago

    Swansea, City and County of Swansea, United Kingdom The Recruitment Co. Full time

    The Recruitment Company is seeking a dedicated Study Monitor for Clinical Operations to join a dynamic team within a prestigious technical products manufacturer. This permanent position offers a competitive salary of £28,017 per annum, with full-time shifts. Key Responsibilities: * Monitor and oversee progress of clinical and application research/trials *...

  • Study Monitor

    6 days ago

    Swansea, City and County of Swansea, United Kingdom Cyden Ltd Full time

    Job Title: Study MonitorWe are seeking a highly skilled Study Monitor to join our Clinical and Application Research Team at Cyden Ltd.Job Purpose:The successful candidate will be responsible for overseeing the progress of clinical and application research/trials, ensuring all research is conducted, recorded, and reported in accordance with Protocols, SOPs,...

  • Study Monitor

    6 days ago

    Swansea, City and County of Swansea, United Kingdom Cyden Ltd Full time

    Job Title: Study MonitorWe are seeking a highly skilled Study Monitor to join our Clinical and Application Research Team at Cyden Ltd.Job Purpose:The successful candidate will be responsible for overseeing the progress of clinical and application research/trials, ensuring all research is conducted, recorded, and reported in accordance with Protocols, SOPs,...

  • Study Monitor Clinical Operations

    3 days ago

    Swansea, City and County of Swansea, United Kingdom The Recruitment Co. Full time

    {"title": "Study Monitor Clinical Operations", "description": "Job SummaryThe Recruitment Co. is seeking a highly skilled Study Monitor Clinical Operations to join our client\u2019s expanding team. As a key member of the clinical operations team, you will be responsible for overseeing the progress of clinical and application research/trials, ensuring...

  • Study Monitor Clinical Operations

    3 days ago

    Swansea, City and County of Swansea, United Kingdom The Recruitment Co. Full time

    {"title": "Study Monitor Clinical Operations", "description": "Job SummaryThe Recruitment Co. is seeking a highly skilled Study Monitor Clinical Operations to join our client\u2019s expanding team. As a key member of the clinical operations team, you will be responsible for overseeing the progress of clinical and application research/trials, ensuring...

  • Study Monitor

    4 months ago

    Swansea, United Kingdom Cyden Ltd Full time

    **Overall job purpose**: 2.Ensure all research is conducted, recorded, and reported in accordance with Protocols, SOPs, ICH-GCP and applicable regulatory requirements. 3.Provide a global evaluation of all investigations commissioned and executed. **Background**: We are looking for a Study Monitor to join our expansive Clinical and Application Research...

  • Study Monitor

    4 months ago

    Swansea, United Kingdom Cyden Ltd Full time

    Overall job purpose:1.Oversee the progress of clinical and application research/trials.2.Ensure all research is conducted, recorded, and reported in accordance with Protocols, SOPs, ICH-GCP and applicable regulatory requirements.3.Provide a global evaluation of all investigations commissioned and executed.Background:We are looking for a Study Monitor to join...

  • Clinical Research Associate

    4 months ago

    Swansea, United Kingdom ICON Full time

    **Role: Clinical Research Associate** **Location: South West of the UK (Swansea, Cardiff, Swindon, Bristol and Southampton)** **Fully sponsor dedicated** ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us...

  • Clinical Research Associate

    1 week ago

    Swansea, City and County of Swansea, United Kingdom ICON Full time

    Role OverviewAs a Clinical Research Associate at ICON, you will be part of a global team dedicated to delivering high-quality clinical research services to our clients. Your primary responsibility will be to manage investigator sites and monitor activities for assigned clinical studies throughout the trial lifecycle.Key ResponsibilitiesFull ownership of...

  • Clinical Research Associate

    1 week ago

    Swansea, City and County of Swansea, United Kingdom ICON Full time

    Role OverviewAs a Clinical Research Associate at ICON, you will be part of a global team dedicated to delivering high-quality clinical research services to our clients. Your primary responsibility will be to manage investigator sites and monitor activities for assigned clinical studies throughout the trial lifecycle.Key ResponsibilitiesFull ownership of...

  • Clinical Research Coordinator

    2 weeks ago

    Swansea, City and County of Swansea, United Kingdom Cyden Ltd Full time

    {"title": "Study Monitor", "description": "Job SummaryCyden Ltd is seeking a highly skilled Study Monitor to oversee the progress of clinical and application research/trials. The successful candidate will ensure all research is conducted, recorded, and reported in accordance with Protocols, SOPs, ICH-GCP and applicable regulatory requirements.Key...

  • Clinical Research Coordinator

    2 weeks ago

    Swansea, City and County of Swansea, United Kingdom Cyden Ltd Full time

    {"title": "Study Monitor", "description": "Job SummaryCyden Ltd is seeking a highly skilled Study Monitor to oversee the progress of clinical and application research/trials. The successful candidate will ensure all research is conducted, recorded, and reported in accordance with Protocols, SOPs, ICH-GCP and applicable regulatory requirements.Key...

  • Clinical Research Coordinator

    2 weeks ago

    Swansea, City and County of Swansea, United Kingdom Cyden Ltd Full time

    Job SummaryCyden Ltd is seeking a highly skilled and experienced Study Monitor to join our Clinical and Application Research Team. As a Study Monitor, you will play a critical role in ensuring the successful execution of clinical trials and application research projects.Key ResponsibilitiesOversee the progress of clinical and application research/trials,...

  • Clinical Research Coordinator

    2 weeks ago

    Swansea, City and County of Swansea, United Kingdom Cyden Ltd Full time

    Job SummaryCyden Ltd is seeking a highly skilled and experienced Study Monitor to join our Clinical and Application Research Team. As a Study Monitor, you will play a critical role in ensuring the successful execution of clinical trials and application research projects.Key ResponsibilitiesOversee the progress of clinical and application research/trials,...

  • Clinical Trial Assistant

    3 months ago

    Swansea, United Kingdom Acorn Recruitment Limited Full time

    Job Title: Clinical Trial Assistant **Salary**: - £26K per annum Hours: Monday - Friday 37 hours Shifts: 7am - 3pm and 1pm - 9pm these shifts are mixed. Location: Swansea Job description: Our client is looking for a Clinical Trial Assistant to undertake clinical trials for the Company's products, preparing and completing all required records and...

  • Clinical Research Coordinator

    22 hours ago

    Swansea, City and County of Swansea, United Kingdom Cyden Ltd Full time

    Job Title: Study MonitorJob Summary:We are seeking a highly skilled Study Monitor to join our Clinical and Application Research Team at Cyden Ltd. The successful candidate will be responsible for overseeing the progress of clinical and application research/trials, ensuring compliance with protocols, SOPs, ICH-GCP, and regulatory requirements.Key...

  • Clinical Research Coordinator

    24 hours ago

    Swansea, City and County of Swansea, United Kingdom Cyden Ltd Full time

    Job Title: Study MonitorJob Summary:We are seeking a highly skilled Study Monitor to join our Clinical and Application Research Team at Cyden Ltd. The successful candidate will be responsible for overseeing the progress of clinical and application research/trials, ensuring compliance with protocols, SOPs, ICH-GCP, and regulatory requirements.Key...