Clinical Trials Jobs in Berkshire
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Search results - Clinical Trials Jobs in Berkshire
IQVIA-Reading
Specialist plays a key role in ensuring the integrity and reliability of clinical trial data.
This position involves reviewing scales administered by raters to confirm standardized assessment practices.
Responsibilities include evaluating assessment quality...
talent.com -
IQVIA-Reading
minimumon-site monitoring experience of clinical trials within a CRO, pharmaceutical, biotechnology, or healthcare environment.
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• Strong knowledge of GCP, ICH guidelines, and applicable regulatory requirements.
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• Preferrable experience...
ziprecruiter.com -
IQVIA-Reading
is seeking experienced Clinical Data Management Leads to oversee end-to-end data management delivery for global clinical trials.
You’ll ensure quality, accuracy, and compliance while leading cross-functional teams that help bring new therapies to life...
talent.com -
CSL Behring-Maidenhead
It's not a supporting or administrative function — it's the core that determines whether the science translates into a trial that runs cleanly and data that holds up.
What You'll Be Responsible For
You'll take ownership of clinical studies end-to-end...
thebigjobsite.com -
UCB Group-Reading
Make your mark for patientsWe are looking for an Associate Director, Clinical Trial Devices to join us in our Global Regulatory Device Strategy team, based in our office in Belgium, Brussels.About the roleThe Associate Director, Clinical Trial...
talent.com -
IQVIA-Reading
Health Sciences, Nursing, Pharmacy, or a related discipline, or equivalent combination of education and experience.
• 2 years minimumon-site monitoring experience of clinical trials within a CRO, pharmaceutical, biotechnology, or healthcare environment...
CSL Behring-Maidenhead
multiple clinical trials and ensuring consistency of standards and approach
Lead the planning, specification and delivery of integrated analyses (ISS/ISE) and pooled datasets, and own the submission-ready data package, including define.xml, reviewer guides...
thebigjobsite.com -
Clinical Trials – Related jobs in Berkshire:
Reading
Procurement and Estates, becoming a trusted partner and advisor.
• Lead Product Demonstrations & Clinical Evaluations - Deliver engaging product demonstrations, presentations and clinical trials, providing expert guidance and helping customers understand...
cv-library.co.uk -
CSL Behring-Maidenhead
engagement activities that inform study design and patient-facing materials. Your work will help ensure that clinical trials are designed with patients, not just for patients.
Hybrid based (3 days a week office) in Maidenhead (UK)
What You'll Be Responsible...
thebigjobsite.com -
IQVIA-Wokingham
for project execution support as appropriate
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Requirements
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A minimum of 18 months of independent on-site monitoring
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You have successfully managed multiple clinical trial protocols across diverse investigative sites.
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mindmatch.ai -
Reading
Summary
We are seeking an experienced Clinical Systems Business Manager to support global clinical operations, driving the effective use, optimisation and continuous improvement of systems supporting clinical trial delivery.
Working across cross...
cv-library.co.uk -
IQVIA-Reading
minimumon-site monitoring experience of clinical trials within a CRO, pharmaceutical, biotechnology, or healthcare environment.
/n
/n
/n
• Strong knowledge of GCP, ICH guidelines, and applicable regulatory requirements.
/n
/n
/n
• Preferrable experience...
ziprecruiter.com -
IQVIA-Reading
as appropriate
Requirements
• Experience of independent on-site monitoring
• You have successfully managed multiple clinical trial protocols across diverse investigative sites.
• In depth knowledge of Good Clinical Practice (GCP) and International Conference...
IQVIA-Reading
clinical trial protocols across diverse investigative sites.
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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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ziprecruiter.com -
IQVIA-Reading
Health Sciences, Nursing, Pharmacy, or a related discipline, or equivalent combination of education and experience.
• 4 years minimumon-site monitoring experience of clinical trials within a CRO, pharmaceutical, biotechnology, or healthcare environment...
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