Clinical Trials Jobs in Berkshire
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Search results - Clinical Trials Jobs in Berkshire
Skills Alliance-Slough
Clinical Trial Manager (Contract) | Cell Therapy / Oncology | UK Hybrid
We are seeking an experienced Clinical Trial Manager to join a leading biotechnology organisation on a 12-month contract basis.
📍 Location: Stockley Park, UK (Hybrid – 3...
Ora-Slough
are critical in driving clinical ophthalmic projects forward utilizing best practices in order to ensure budgets, timelines, and clinical trial requirements are being met on behalf of the sponsor. This role will work independently to manage cross functional...
Indo Search-Slough
Clinical Trial Assistant
London | £30,000 to £35,000 | Primarily Site Based
This is a genuinely hands on clinical research position where you will work directly with study participants, support treatment sessions, coordinate clinical visits...
IQVIA-Reading
trial protocols across diverse investigative sites.
• In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Life science degree educated or equivalent industry experience
• Flexibility...
i-Pharm Consulting-Slough
Clinical Trial Manager (CTM) – 6-Month Contract
Location: London, UK (Hybrid)
A global leader in rare genetic disease therapeutics is seeking an experienced Clinical Trial Manager (CTM) to join their Global Study Operations team on a 6-month...
IQVIA-Reading
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...
BioTalent-Slough
statistical, data visualisation, and scientific communication skills
Additional experience in spatial omics, epigenomics, proteomics, containerisation technologies, or clinical trial datasets would be highly valued.
This is a UK-based role with hybrid...
Clinical Trials – Related jobs in Berkshire:
IQVIA-Bracknell
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...
IQVIA-Reading
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...
Reading
clinical trial protocols across diverse investigative sites.
In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Life science degree educated or equivalent industry experience
Flexibility...
cv-library.co.uk -
IQVIA-Reading
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...
2 similar jobs: Manchester, Chesterfield
Wokingham
clinical trial protocols across diverse investigative sites.
In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Life science degree educated or equivalent industry experience
Flexibility...
cv-library.co.uk -
IQVIA-Bracknell
trial protocols across diverse investigative sites.
• In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Life science degree educated or equivalent industry experience
• Flexibility...
IQVIA-Wokingham
trial protocols across diverse investigative sites.
• In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Life science degree educated or equivalent industry experience
• Flexibility...
CSL Behring-Maidenhead
The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. The AD provides statistical strategies for the clinical trials and regulatory submissions and is accountable...
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