Biomedical Scientist jobs in Derby
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
- View all IQVIA jobs - Nottingham jobs
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- PepsiCoLeicester LE4 1ET
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- We are looking for enthusiastic undergraduates to join our R&D teams on a 12-month placement programme starting in July 2027 on a full-time basis.
- We are looking for enthusiastic undergraduates to join our R&D teams on a 12-month placement programme starting in July 2027 on a full-time basis.
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- Electronics Assembly Solutions - Innovating semiconductor, surface mount technology, and power electronics assembly for unparalleled reliability.
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- LearndAshby-De-La-Zouch LE65 1NF
- Learnd is seeking a Project Sales Manager to join the team in the Midlands area.
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- Albireo EnergyDerby
- The role combines advanced service engineering with responsibility for identifying, pricing, and delivering improvement works.
- Bravo Benefits and EAP Scheme.
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- Brightwake LtdKirkby in Ashfield NG17 7JZ
- We are currently looking for a full-time Technician to work withing our Project Test Lab.
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- University Hospitals of Derby and Burton NHS...Derby DE22 3NE
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- University Hospitals of Derby and Burton NHS...Derby DE22 3NE
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- Excellerate Bioscience LtdNottingham NG2 1AE
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Clinical Research Associate
Job details
Job type
Full job description
Nottingham, United Kingdom | Full time | Field-based | R1514135
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
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Experience of independent on-site monitoring of Oncology therapeutic area for unblinded studies.
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In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
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Life science degree educated or equivalent industry experience
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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.
Where you'll work
Field-based
You’ll work where the action is — out in the field, directly engaging with our customers, sites or partners. Field-based roles offer the opportunity to build relationships face-to-face, gain real-world insights and make a tangible impact.
Culture
Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.