CLINICAL TRIALS STUDY START jobs in UNITED KINGDOM, United Kingdom

business development, initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements... of clinical study approvals, authorizations and review/ negotiation of contracts and essential documents. Work with Quality...

Job Summary Our clinical operations activities are growing rapidly and we are currently seeking full-time, Regulatory... Submissions Technical Advisors to join our Site Activation and Maintenance team, within Clinical Operations. This position plays...

, with a strong emphasis on the EMEA region. The successful candidate will be a member of the Global Study team overseen by a Clinical Program... Manager. The candidate will likely work across several studies, including involvement from study start-up through study...

lives. Read more: The Submission Manager, Clinical Trials manages and coordinates the timely, compliant, and accurate... of trials and CSR distributions. Ensure consistency of the Clinical Trial application across projects, studies and countries...

lives. Read more: Position Purpose The Submission Manager, Clinical Trials manages and coordinates the timely, compliant... of trials and CSR distributions. Ensure consistency of the Clinical Trial application across projects, studies and countries...

About the role 100,000+ That's how many patients participate in our clinical trials at any given time. Global... trials to deliver study outcomes within schedule, budget, quality/compliance, and performance standards. You will implement...

provision of nursing support and duties for optimal study delivery from clinical start-up to clinical close out... and execution of a clinical study screening. hVIVO conducts human challenge studies offering services to both pharmaceutical...

oversight of clinical study execution in accordance with the global program strategy, through leadership of the cross-functional... documents. Accountable for site-level goal setting and study-specific deliverables for clinical sites within their country(ies...

clinical trials, track study progress and ensure timely quality updates are provided. Your responsibilities will include...The Recruitment Co are recruiting for a Study Monitor (Clinical Operations) to join our clients expanding team. A world...

. You will maintain all files pertaining to the clinical trials, track study progress and ensure timely quality updates are provided...Overall job purpose: 1.Oversee the progress of clinical and application research/trials. 2.Ensure all research...

of clinical trials from start-up through close out. Manage the technical, financial and operational aspects of projects. Drive.... We have successfully run trials across the UK, Europe and beyond, tailoring our clinical research services to meet our client...

business development, initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements... of clinical study approvals, authorizations and review/ negotiation of contracts and essential documents. Work with Quality...

of clinical trials across a complex programme. Lead the development and review of data management processes (e.g. process... quality and completeness of data Study status reporting (e.g., provide data to clinical teams for performing medical...

. It is preferred you have experience or an interest in the conduct of clinical trials but not essential.... Ensure clinical and regulatory compliance. Ensure each participant journey and their individual experience is to the highest...

Abbott Diabetes Care regarding the conduct of clinical investigations at study sites across the UK and possibly..., and study start up. You should be excited about working in a fast-paced environment within a hard-working and welcoming team...

internal stakeholders Collaborates and interact with QA, Global Monitoring, clinical Study Start-Up teams, Global Clinical... are reached and potential country issues properly followed-up. Collaborate and liaise with Clinical Study Teams and Global...

products – Ability to navigate regulatory procedures for marketing applications, clinical trials, and post-approval changes...) Clinical Study Team (CST) Label Working Group (LWG) Regional Teams (e.g. IMT, IBT, NAMT) Benefits: – Opportunity to work...