Site Monitoring Professional

3 weeks ago


Reading, Reading, United Kingdom IQVIA Argentina Full time
Be Part of Our Sponsor-Dedicated Team as a Clinical Research Associate

IQVIA is seeking talented Clinical Research Associates to join our team, providing support to sites across Scotland and Northern England. This role offers a unique opportunity to work on various projects, develop your skills, and grow your career.

We are looking for candidates who are passionate about research, have excellent communication skills, and can work independently. You will have a strong understanding of GCP and ICH guidelines, which will enable you to perform site monitoring visits, adapt recruitment plans, and administer protocol training effectively.

About the Role

As a Clinical Research Associate, you will be responsible for managing study progress, tracking regulatory submissions, recruitment, and data query resolution. You will also evaluate site practices, ensuring compliance with regulatory requirements and company standards.

We offer a competitive salary of £40,000 - £55,000 per annum, depending on experience, plus benefits including flexible working hours, technology-enabled resources, and opportunities for career growth.

Key Responsibilities
  • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution
  • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations
  • Escalate quality issues as appropriate


  • Reading, Reading, United Kingdom Pharmiweb Full time

    **Job Overview:** UK On-Site Monitoring ProfessionalWe are seeking a skilled UK On-Site Monitoring Professional to join our team in the UK. As a key member of our clinical research services team, you will be responsible for conducting on-site monitoring activities to ensure the quality and integrity of clinical trials.**Key Responsibilities:Conduct on-site...


  • Reading, Reading, United Kingdom IQVIA, Inc. Full time

    IQVIA, Inc. is expanding its Site Monitoring Expert team and seeking an experienced professional to join us. As a Site Monitoring Expert, you will perform site monitoring visits, work with sites to adapt and drive subject recruitment plans, and evaluate the quality and integrity of study site practices.The ideal candidate will have a life science degree...


  • Reading, Reading, United Kingdom IQVIA Full time

    We are seeking a talented Site Monitoring Specialist to join our team in Northern England and Scotland. As a key member of our sponsor-dedicated team, you will play a crucial role in supporting sites across the region.Job SummaryAs a Site Monitoring Specialist, you will be responsible for performing site initiation, monitoring, and close-out visits, adapting...


  • Reading, Reading, United Kingdom IQVIA Argentina Full time

    Job Description:We are seeking a highly motivated and experienced Site Monitoring Expert to join our team. As a Site Monitoring Expert, you will be responsible for conducting site monitoring visits to ensure the integrity of clinical trials. You will work closely with sites to adapt and drive subject recruitment plans, track regulatory submissions, and...


  • Reading, Reading, United Kingdom IQVIA Full time

    Job OverviewWe are seeking an experienced Site Monitoring Specialist to join our cFSP (sponsor-dedicated) team at IQVIA UK. The successful candidate will be responsible for performing site monitoring visits and ensuring the quality and integrity of study site practices.About Our CompanyIQVIA is a leading global provider of clinical research services,...


  • Reading, Reading, United Kingdom IQVIA LLC Full time

    Clinical Research Associate - South West EnglandWe are looking for a seasoned Clinical Research Associate to join our team in the South West of England, supporting sponsors and advancing patient care.About This RoleThis position presents an exceptional opportunity for CRAs to grow professionally, leverage industry expertise, and contribute to groundbreaking...


  • Reading, Reading, United Kingdom IQVIA Full time

    We are seeking a Site Monitoring Expert to join our team in the South West of England. In this role, you will be responsible for performing site monitoring visits, adapting and driving subject recruitment plans, and evaluating the quality and integrity of study site practices.About IQVIAIQVIA is a leading global provider of clinical research services,...

  • Site Monitor Expert

    4 weeks ago


    Reading, Reading, United Kingdom Pharmiweb Full time

    Pharmiweb Career OpportunityWe are seeking an experienced Clinical Research Associate to join our dynamic team at Pharmiweb. As a Clinical Research Associate, you will play a critical role in ensuring the successful execution of clinical trials by conducting site monitoring visits, adapting subject recruitment plans, and evaluating study site practices.To...

  • Site Monitor

    2 weeks ago


    Reading, Reading, United Kingdom Randstad Construction & Property Full time

    Job DescriptionWe are seeking a skilled Banksman to join our team at Randstad Construction & Property.Salary: £50 per hour, competitive and based on experience.About the Company: As a well-established construction company in the UK, we pride ourselves on delivering high-quality workmanship and meeting project deadlines.Key Responsibilities:Monitor traffic...


  • Reading, Reading, United Kingdom IQVIA Full time

    Job Overview:We are seeking a highly skilled Clinical Research Associate to join our team in the South West of England. As a Clinical Research Associate, you will be responsible for performing site monitoring visits in accordance with contracted scope of work and regulatory requirements.You will work with sites to adapt, drive, and track subject recruitment...


  • Reading, Reading, United Kingdom IQVIA, Inc. Full time

    About the RoleWe are looking for an experienced Clinical Research Associate to join our team at IQVIA, Inc.The ideal candidate will have a strong background in clinical research and excellent communication skills.Responsibilities:Conduct site monitoring visits to ensure compliance with regulatory requirements.Collaborate with sites to develop and implement...


  • Reading, Reading, United Kingdom IQVIA Argentina Full time

    About the RoleWe are looking for a skilled Clinical Research Associate to join our sponsor-dedicated team in the South West of England.As a Clinical Research Associate, you will be responsible for performing site monitoring visits and ensuring the quality and integrity of study site practices.You will work closely with sites to adapt and track subject...


  • Reading, Reading, United Kingdom IQVIA Full time

    Skillful Site Monitoring Experts are required to join our team at IQVIA, working in Northern England and Scotland. This position offers an excellent opportunity to utilize your expertise in clinical research, collaborating with supportive leadership and cutting-edge technology.Job RequirementsLife science degree or equivalent industry experience6 months of...

  • Research Associate

    4 weeks ago


    Reading, Reading, United Kingdom IQVIA LLC Full time

    Clinical Research AssociateWe are seeking a Clinical Research Associate to join our sponsor-dedicated team and support sites across Northern England and Scotland.This is an excellent opportunity for CRAs local to Northern England or Scotland who would value:Supportive leadership and collaborative teamsA variety of career opportunities to allow you to grow as...


  • Reading, Reading, United Kingdom CV Library Full time

    Site Management ProfessionalWe are looking for a skilled Site Management Professional to join our team at CV Library. As a Site Management Professional, you will be responsible for site coordination, ensuring smooth project execution and delivery. Your key responsibilities will include:Site Coordination:Manage site logistics, including planning, scheduling,...


  • Reading, Reading, United Kingdom IQVIA Argentina Full time

    About the JobIn this role, you will work with sites to adapt, drive, and track subject recruitment plans, and manage the progress of assigned studies by tracking regulatory submissions and approvals. You will also ensure that site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is...


  • Reading, Reading, United Kingdom AWE Plc Full time

    AWE Plc has an exciting opportunity for a Condition Monitoring Professional to join their team at their RG7 4PR location. This role involves monitoring and analysing equipment performance to identify potential issues before they become major problems.The successful candidate will be responsible for developing and implementing condition-based maintenance...


  • Reading, Reading, United Kingdom IQVIA Argentina Full time

    OverviewIQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry.About the RoleWe are looking for a skilled Clinical Research Associate to join our team in Argentina. As a CRA, you will be responsible for conducting site monitoring visits, administering protocol and related...


  • Reading, Reading, United Kingdom CV-Library Full time

    CV-LibraryWe are seeking a highly skilled Project Monitoring Specialist to join our team. This is a great opportunity for an experienced professional to take on a challenging role and contribute to the success of our projects.The ideal candidate will have excellent project management skills, with experience in delivering complex refurbishment and fit out...


  • Reading, Reading, United Kingdom AWE Plc Full time £35,470 - £45,000

    AWE Plc is currently seeking a qualified Reliability and Condition Monitoring Professional to join our Condition Based Maintenance Team.This role involves managing databases, analysing data, reporting findings and recommendations, managing defect rectifications, and coaching /mentoring practitioners within our team.The ideal candidate should have ISO 18436...