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Clinical Research jobs in Wigan

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    • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
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    • Assist clinical staff members in various clinical activities as required.
    • As the successful role holder you will play a pivotal part in delivering high-quality…
  • View similar jobs with this employer
    • Assist clinical staff members in various clinical activities as required.
    • As the successful role holder you will play a pivotal part in delivering high-quality…
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    • Clinical research: 2 years (required).
    • Minimum 2–3 years clinical research experience.
    • Bodyline Medical Wellness Clinics is a leading CQC-registered clinical…
    • Lead high-value scientific discussions with specialists across multiple disciplines, sharing the latest clinical evidence and contributing to the advancement…
    • As a key ambassador for Hologic, you will engage with international KOLs, support advisory boards and investigator-initiated research, and help position…
    • Conduct research visits and clinical assessments.
    • This role plays a pivotal part in delivering high-quality clinical research across a range of therapeutic…
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    • Significant experience as a Principal Investigator in clinical research.
    • Strong knowledge of ICH-GCP and UK clinical research regulations.
  • View similar jobs with this employer
    • Clinical research: 2 years (required).
    • Minimum 2–3 years clinical research experience.
    • Bodyline Medical Wellness Clinics is a leading CQC-registered clinical…
    • Excellent written communication skills, including experience producing comprehensive clinical reports.
    • Maintain comprehensive and confidential clinical records…
    • This often involves supporting clinical teams in reviewing their caseload to identify suitable participants, contribute to multi-disciplinary meetings to ensure…
    • To supervise the Band 4 OPD research assistant and other junior staff, interns, or peer researchers as needed.
    • An understanding of the clinical research process would be an advantage but if not, these posts will initially be offered at Band 5 to allow training and…
    • Successful applicants will divide their time between research and a moderate clinical commitment; this may involve clinical research and audit activities,…
    • Provide professional and management leadership to support the development of clinical research activity for defined research teams.

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Job Post Details

Clinical Research Associate - job post

IQVIA
3.7 out of 5 stars
Manchester
Full-time
You must create an Indeed account before continuing to the company website to apply

Job details

Job type

  • Full-time

Location

Manchester

Full job description

IQVIA's Site Management (multi-sponsor) team are seeking a Clinical Research Associate to join us on our mission to help create a healthier world.

The Clinical Research Associate will support Oncology studies and cover sites across the UK

Apply today and forge a career with greater purpose, make an impact and never stop learning!

Responsibilities

  • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
  • Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
  • Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
  • 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.
  • 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. May support start-up phase.
  • Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
  • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
  • Collaborate and liaise with study team members for project execution support as appropriate.

Requirements

  • Experience of independent on-site monitoring of Oncology therapeutic area for unblinded studies.

  • In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

  • Life science degree educated or equivalent industry experience

  • Flexibility to travel to sites as required

*Please note - this role is not eligible for visa sponsorship*

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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