Live clinical research associate roles in Reading, with South East salary benchmarks.
Reading
IQVIA is seeking a Lead Medical Writer in Reading to drive major writing projects such as CSRs and protocols, ensuring adherence to SOPs and client…
Reading
Acts as Lead Medical Writer on most types of writing projects.
Reading
ICON is a global healthcare intelligence and clinical research organisation seeking a Senior Statistical Analyst to join the Real World Evidence…
Reading
ICON is a global healthcare intelligence and clinical research organisation seeking a Senior Statistical Analyst to join the Real World Evidence…
Reading
Baxter International Inc. in the UK, Ireland and Malta seeks a Country Quality Assurance (CQA) & Regulatory Affairs (RA) Manager to lead Quality and…
Reading
Baxter International Inc. in the UK, Ireland and Malta seeks a Country Quality Assurance (CQA) & Regulatory Affairs (RA) Manager to lead Quality and…
Reading
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study…
Reading
IQVIA is seeking a Site Monitor to perform monitoring visits, manage site relationships and ensure study data quality in accordance with GCP, ICH…
Reading
Sanofi in the UK is seeking a Student Clinical Project Assistant to support the Clinical Studies Unit with administrative tasks across feasibility…
Reading
Sanofi offers an industrial placement in Regulatory Affairs at our Reading Head Office.
Reading
IQVIA Holdings Inc. in Reading is offering a paid internship as part of the Graduate Programme CRA training track.
Reading
Sanofi is offering a Medical Affairs Industrial Placement in Reading for 13 months, with a hybrid work model (3 days per week in the Reading office…
Reading
Join IQVIA on our mission to accelerate innovation for a healthier world!
Reading
IQVIA in Reading, Berkshire, United Kingdom is seeking a Clinical Trials Assistant (CTA I or CTA II) to support clinical studies by maintaining…
Reading
In this role you will support the Clinical Trial Operational team to execute trials across therapeutic areas.
Reading
IQVIA in Reading, UK, is hiring a Technical Designer responsible for study build, design, and eCRF configurations within CDMS tools.
Reading
Support the day-to-day processing of patient safety information, ensuring records are accurate and completed within required timelines.
Reading
Sanofi-aventis Groupe is offering a placement in the Pharmacovigilance team in the UK.
Reading
Sanofi is seeking a Student Clinical Project Assistant in Reading to join the Clinical Studies Unit.
Reading
STADA UK Thornton & Ross is on an exciting growth journey with more than 700 employees being fully committed to our purpose of Caring for People’s…
Reading
STADA UK Thornton & Ross is on an exciting growth journey with more than 700 employees being fully committed to our purpose of Caring for People's…
Reading
STADA UK Thornton & Ross invites applications for a Pharmacovigilance Placement Student in Reading, UK.
Reading
STADA UK Thornton & Ross is offering a Medical Affairs Placement Student role in Reading for 12 months, commencing July 2027, with a salary of…
Reading
Sanofi offers an industrial placement in Regulatory Affairs at Reading (Head Office).
Reading
In this role you drive site monitoring across interventional studies, ensuring GCP/ICH compliance and high-quality data.
Reading
IQVIA in Reading, UK is seeking a Clinical Supply Chain Manager to shape end-to-end supply strategy for new clinical trials.
Reading
IQVIA is seeking a Clinical Supply Chain Manager to shape end-to-end supply strategy for new clinical trials in Reading, UK.
Reading
Kenvue is recruiting for Regulatory Affairs Industrial Placements in the UK, based at Reading HQ.
Reading
IQVIA is seeking a Senior Clinical Research Associate (cFSP sponsor-dedicated) in Reading to monitor sites and manage study data per protocol and GCP.
Reading
Reading
The Clinical Project Manager (Sponsor dedicated) will be leading Local Study Teams at country level to deliver committed components of clinical…
Reading
IQVIA LLC seeks a Principal Medical Writer to act as Lead Medical Writer on a range of writing projects.
Reading
Apply: Reading, Berkshire, United Kingdom: Lisbon, Portugal: Brussels, Brussels-Capital Region, Belgium: Belgrade, Serbia: Barcelona, Spain: Full…
Reading
Join Us on Our Mission to Drive Healthcare ForwardIQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.With…
Reading
We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation.
Reading
We are a pharmaceutical company specialising in the research, development, manufacture and distribution of medicines.
Reading
PAION Pharma in the UK is seeking an enthusiastic MSL to join our Medical Affairs team.
Reading
ICON plc is seeking a Study Start Up Manager for the UK to lead and oversee clinical trial start-up activities, ensuring regulatory compliance and…
Counted from the adverts on this board, refreshed hourly. Advertised pay is what employers state, not a market survey.
£42,000 – £65,000 (indicative · midpoint £53,500)
How this figure was built. No live advertised salaries back this figure yet. It is the midpoint of our curated 2026 baseline range for the role and region.
Methodology: medians reconcile live advertised UK salaries for this role and region; 25th–75th percentiles are shown only where at least 5 live salaried listings back them. They are measured or omitted, never interpolated. Rows marked indicative are anchored to our curated 2026 baseline ranges until enough live data accrues. Listings advertising an implausible annual figure (a mislabelled hourly or daily rate) are excluded rather than converted, because converting one means guessing the hours behind it.
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