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Clinical Trials Jobs in Maidenhead

1 - 15 of 31
1 - 15 of 31
Search results - Clinical Trials Jobs in Maidenhead
Maidenhead
The role Fortrea is currently seeking a pro-active Clinical Trial Administrator to join our expanding team in London. This client-dedicated role is to be office based in central London for at least 3 days a week with the rest of the time being...
pharmiweb.jobs -
Maidenhead
Location: Maidenhead  •  Pay: £100-£105 per day, Monday to Friday, term time only  •  Start Date: June/July and September 2025 - trial for September before hand.  •  Contract: Full-time, Monday to Friday (8:30 am – 3:45pm) Are you a Psychology or Criminology...
cv-library.co.uk -
Maidenhead
in groundbreaking clinical trials while being part of a supportive, fast-paced and innovative global CRO. What You Can Expect: ✅ National monitoring across the UK (remote-based) ✅ Oncology focus, including solid tumor studies, Prostate, NSCLC, Leukemia, Breast...
pharmiweb.jobs -
Pharmiweb-Maidenhead
skills.  •  In depth knowledge of clinical trial process and data management, clinical operations, biometrics, quality management, and systems applications to support operations.  •  Working knowledge of the relationship and regulatory obligation of the CRO...
theguardian.com -
PHASTAR-England
Programming Experience within the pharmaceutical industry  •  Have to have worked on Disclosure tables especially the Basic Results tables.  •  Good awareness of clinical trial issues, design, and implementation.  •  Familiarity with GCP and regulatory requirements...
Maidenhead
activation for clinical trials! Summary of Responsibilities: ✔ Serve as a primary contact expert for a dedicated Client, to perform Country Level start-up and maintenance activities/amendments of Clinical Trials in the UK (ROI applications knowledge also...
pharmiweb.jobs -
Pharmiweb-Maidenhead
knowledge of clinical trial process and data management, clinical operations, biometrics, quality management, and systems applications to support operations.  •  Working knowledge of the relationship and regulatory obligation of the CRO industry...
theguardian.com -
Little Journey-England
the presence of our patient engagement platform in paediatric clinical trials. You will be responsible for driving new business growth, managing complex sales cycles, and building strategic relationships with senior stakeholders in Pharma R&D, Medical Affairs...
workable.com -
Alnylam Pharmaceuticals-Maidenhead
of the lifecycle of a defined portfolio of products.Guide the clinical development teams regarding all aspects of clinical safety, including trial design, appropriateness of safety endpoints, analysis, and interpretation of safety data.Be accountable for timely...
riskjobsite.co.uk -
Outcomes First Group-England
How would you like to be paid for five days but only work four*? Our colleagues’ wellbeing is at the heart of everything we do at OFG, so we’re always looking for new ways to improve everyone’s work/life balance. We’re taking part in a trial...
Outcomes First Group-England
How would you like to be paid for five days but only work four*? Our colleagues’ wellbeing is at the heart of everything we do at OFG, so we’re always looking for new ways to improve everyone’s work/life balance. We’re taking part in a trial...
jmmst.com -
Outcomes First Group-England
How would you like to be paid for five days but only work four*? Our colleagues’ wellbeing is at the heart of everything we do at OFG, so we’re always looking for new ways to improve everyone’s work/life balance. We’re taking part in a trial...
Maidenhead
clinical operations team, playing a pivotal role in initiating and supporting clinical trials across the UK. Key Responsibilities:  •  Lead and coordinate all aspects of study start-up, from site identification to activation  •  Manage Health Authority...
pharmiweb.jobs -
Little Journey-England
scalable content—both digital and physical—for international healthcare organisations and clinical trials that incorporate behaviour change frameworks. You will liaise with a small group of freelance copywriters, agencies and our internal team.   2.  Product...
workable.com -
Michael Page-England
of regulatory submission documents including orphan drug designation applications, scientific advice briefing documents, clinical trial applications and investigational new drug applications, PIPs/PSPs, PRIME/BTD/RMAT and marketing authorisation applications...
michaelpage.co.uk -
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