Clinical scientist jobs in Reading

Our client is recruiting for a high caliber scientist to join the team to support clinical transcriptomics as a Subject Matter Expert. * The successful applicant will be responsible for planning and ...

As a Scientist you will join the Biomarker Assay Sciences group which is positioned within the Early Clinical Development & Translational Science (ECD&TS) department that completes research from ...

Clinical Scientist, Medical Device Researcher, Clinical Affairs Specialist, Regulatory Research Analyst, Biomedical Researcher, Scientific Data Analyst, Clinical Study Coordinator, Medical Research ...

... experience ideally in clinical trials and CTR submission experience would be preferred. Job ... Sciences degree or equivalent • Ideally 12 months of previous RA experience dedicated to CTA

A degree in a scientific discipline * Background in clinical trial management * Experience in Regulatory Affairs * Good level of knowledge of Clinical Trial Submissions on a local and regional level

... experience ideally in clinical trials and CTR submission experience would be preferred. Job ... Life Sciences degree or equivalent * 12 months of previous RA experience dedicated to CTA's. Please ...

Life Sciences Recruitment is pleased to confirm that we are working with our global, fast-growing clinical trial supply (CTS) client, to hire a Project Manager to join their Unlicensed Medicines ...

If you are a confident Quality Professional, or a very experienced clinical diagnostics scientist with strong quality experience, then you may be suitable for this role. Unfortunately, pure ...

Oxford Nanopore Technologies is headquartered at the Oxford Science Park outside Oxford, UK, with ... Experience within a clinical software environment * Experience writing tests at different levels of ...

Ensure the submission strategy for clinical trials planned globally are in accordance with the ... sciences subject is required

Our client is looking for an experienced Clinical Pharmacist in Primary Care who is a qualified ... Science sectors.

Ensure the submission strategy for clinical trials planned globally are in accordance with the ... A Degree in medicine, pharmacy, biology, chemistry, pharmacology, or related life sciences subject ...

If you have a Psychology / Criminology / Social Science degree, it's an excellent use of your degree **You MUST have right to work in the UK in order to apply - no Visa sponsorship

If you have a Psychology / Criminology / Social Science degree, it's an excellent use of your degree **You MUST have right to work in the UK in order to apply - no Visa sponsorship

If you are a confident Quality Professional, or a very experienced clinical diagnostics scientist with strong quality experience, then you may be suitable for this role. Unfortunately, pure ...

Bachelor's Degree required, preferably in the life sciences, pharmacy, nursing, or other scientific background * 5+ years of work experience in a cGMP related industry or in a clinical setting ...

These groups specialise in developing clinical and regulated products. The bioinformatics analyst ... Work collaboratively with laboratory scientist, workflow developers and other data analysts to ...

The authoring of high quality regulatory required aggregate reports including scientific analysis ... Clinical Development Integrations Support Integrations of Global Aggregate Report office and PV ...

Ensure that all the required approvals are acquired and maintained in order to support clinical ... Educated to degree level or above in life sciences or a relevant field with significant experience ...

Preference for knowledge and experience in medical device legislation relevant to clinical trials. * Holds a degree in medicine, pharmacy, biology, chemistry, pharmacology, or a related life sciences ...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and ...

Relevant advanced degree in life sciences is preferred § At least 2-years CTA experience in global clinical trial submissions to regulatory agencies. § Experience working effectively across ...

Understanding of the clinical drug development process. * Proficiency in statistical programming ... Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and ...

... natural science or equivalent number of years' experience · Experience in Pharmacovigilance auditing (Qualification as an auditor preferred) · Several years of clinical/industry/Regulatory ...