87

Clinical data associate jobs in Oxfordshire

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Associate Director Clinical Quality Assurance (GCP) OXFORDSHIRE, GB ...them in a search for an Associate DIrector of Clinical Quality Assurance (GCP). The successful candidate will be reporting directly to the Head of QA and spearhead all activities related to GCP. Main Duties and Responsibilities include: Ensuring changes in GCP practices are communicated, adopted...
Associate Director, Regulatory Affairs CMC £80 - 100 ABINGDON Job Details: Associate Director, Regulatory Affairs CMC p Full details of the job. /p p Vacancy Name /p p Vacancy Name Associate Director, Regulatory Affairs CMC /p p Vacancy No /p p Vacancy No VN194 /p p Employment Type /p p Employment Type Permanent /p p Location of role /p...
Associate Director Clinical Quality Assurance (GCP) OXFORDSHIRE, SOUTH EAST ENGLAND ...them in a search for an Associate DIrector of Clinical Quality Assurance (GCP). The successful candidate will be reporting directly to the Head of QA and spearhead all activities related to GCP. /p p br /p p b Main Duties and Responsibilities include: /b /p p br /p ul li Ensuring...
Looking for Clinical Data Associate jobs in Oxfordshire? Top Salaries! Full time, part time and contract. OXFORDSHIRE Visit PerfectJobs4U UK for the widest selection of top UK jobs. Full time, part time and work from home roles.

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Field Research Associate BASINGSTOKE, ENG, GB ...for a Field Research Associate to join our multi-disciplinary R&D Team based at our Head Office in Basingstoke. br / This role is offered on a hybrid working pattern, with the expectation of two days per week in the office and some ad-hoc travel to our UK clinics as required. br / What can we...
Clinical Data Associate SURREY, GB My client are looking for a highly motivated Clinical Data Associate to join their high achieving Clinical Operations and Data Management Team. This is a superb opportunity to kick-start your career working directly in house for a leading global pharmaceutical company Key Responsibilities: Fully...
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Regulatory Manager, Clinical Trial Strategy & Submissions MAIDENHEAD, GB We re currently recruiting for a Regulatory Clinical Trial Strategy & Submissions Manager for a Global Pharmaceutical Company who have opened a new vacancy within their Regulatory Affairs team on an initial 12 Month basis to be based at their office in Maidenhead/hybrid. The Role: Deliver CTA...
Manager, Clinical Trial Strategy & Submissions, Regulatory Operations MAIDENHEAD, GB ...submission strategy for clinical trials planned globally are in accordance with the overarching global regulatory strategy and any risks and issues are highlighted to the Global Regulatory Project Team and study teams. Ensure study deliverables are achieved in accordance with global regulatory...
Clinical Risk Solicitor or Associate SOUTHAMPTON, GB Our Clinical Risk cluster is the biggest nationally- handling a challenging but fulfilling caseload of defendant clinical negligence work- acting for a variety of clients, which may include work for NHS Resolution, NHS Trusts, MDU, independent providers, and medical malpractice insurers. We pride...
Clinical Data Associate SURREY, SOUTH EAST ENGLAND p My client are looking for a highly motivated b Clinical Data Associate /b to join their high achieving Clinical Operations and Data Management Team. This is a superb opportunity to kick-start your career working directly in house for a leading global pharmaceutical company /p p br /p p b...
Associate Director, Clinical Pharmacology SURREY, ENGLAND, UNITED KINGDOM ...About the role The Associate Director, Clinical Pharmacology is responsible for leading clinical research activities with focus on clinical pharmacology phase I pharmacokinetics and bioequivalence trials. He/she will ensure that high quality expertise is provided to meet state-of-the-art...
Field Research Associate BASINGSTOKE, SOUTH EAST ENGLAND ...for a Field Research Associate to join our multi-disciplinary R&D Team based at our Head Office in Basingstoke. /p p br /p p This role is offered on a hybrid working pattern, with the expectations of two days per week in the office and some ad-hoc travel to our UK clinics as required. /p p...
Manager, Clinical Trial Strategy & Submissions, Regulatory Operations MAIDENHEAD, SOUTH EAST ENGLAND ...submission strategy for clinical trials planned globally are in accordance with the overarching global regulatory strategy and any risks and issues are highlighted to the Global Regulatory Project Team and study teams. /li li Ensure study deliverables are achieved in accordance with global...
Clinical Risk Solicitor or Associate SOUTHAMPTON, SOUTH EAST ENGLAND p Our Clinical Risk cluster is the biggest nationally- handling a challenging but fulfilling caseload of defendant clinical negligence work- acting for a variety of clients, which may include work for NHS Resolution, NHS Trusts, MDU, independent providers, and medical malpractice insurers. /p p...
Occupational Therapist Associate LONDON, SOUTH EAST ENGLAND p b Why Orri? /b /p p br /p p Orri is an ambitious, young, fast-growing company committed to changing the way we treat eating disorders in the UK. An exciting opportunity has arisen for the post of b Occupational Therapist Associate /b in eating disorders at Orri. /p p br /p p b Role...
Consultant Psychiatrist Chiltern - East Community Mental Health Team £60 - 80 HIGH WYCOMBE p Oxford Health are looking for a 1.0 WTE consultant psychiatrist to provide clinical leadership to the Chiltern East CMHT. This post has become available in the CMHT due to a consultant moving to another area. The post holder will work alongside two other consultants (total 2.6 WTE including this...
Associate Dentist NEWBURY, ENG, GB Role Description br / br / Associate Dentist br / br / Newbury Dental Practice, 4 The Courtyard, London Road, Newbury, RG14 1JX br / br / Itero Scanner br / Specialist service br / Co-Funding Opportunities br / br / Join the vibrant team at Newbury Dental Practice, a thriving four-surgery site...
Regulatory Manager, Clinical Trial Strategy & Submissions MAIDENHEAD p We’re currently recruiting for a Regulatory Clinical Trial Strategy & Submissions Manager for a Global Pharmaceutical Company who have opened a new vacancy within their Regulatory Affairs team on an initial 12 Month basis to be based at their office in Maidenhead/hybrid. /p p br br...
Manager, Clinical Trial Strategy & Submissions, Regulatory Operations MAIDENHEAD ...submission strategy for clinical trials planned globally are in accordance with the overarching global regulatory strategy and any risks and issues are highlighted to the Global Regulatory Project Team and study teams. /li li Ensure study deliverables are achieved in accordance with global...
Interim Deputy Chief Nurse KT16, OTTERSHAW, SURREY ...post-holder provides clinical leadership in the development of Nursing and Midwifery standards and practice that personifies excellence in the delivery of care, and in line with regulatory standards. The post-holder ensures that patients, their relatives and carers have a positive experience...
General Practitioner Up to £118,000 a year BASINGSTOKE, ENG, GB ...nursing and nursing associate trainees and are keen to support our team through additional training meaning lots of opportunities to be involved in developing colleagues. The are a host of specialist clinics and hubs across the sites, including women’s health, vasectomy, frailty, leg...
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