SENIOR CLINICAL TRIAL EXPERT jobs in United Kingdom

the global Clinical Trial Application dossier and subsequent substantial amendments to country applicants and CROs... for submission to ECs and HAs. Prepare the data required in CTIS for global Clinical Trial Application dossiers...

on , , , and . Job Description As a Senior Clinical Trial Manager, you will be part of a dynamic, centralized study management team that is responsible for the... execution of our global clinical trials and a key member of the study team. The Senior CTM works as an independent...

the global Clinical Trial Application dossier and subsequent substantial amendments to country applicants and CROs... for submission to ECs and HAs. Prepare the data required in CTIS for global Clinical Trial Application dossiers...

and expert scientists and oncologists within and external to UCL, and senior staff at the Cancer Institute...About us The Cancer Research UK & UCL Cancer Trials Centre (CTC) is a UKCRC registered and NCRI Clinical Trials Unit...

or maintaining a Clinical Trial Management System? Are you excited about solving clinical trial business problems using modern CTMS... Do Participate in workshops to discuss Clinical Trial Management System requirements with customers Guide customers toward the...

& Medical Negligence Law firm in the East Midlands, and this year they are now listed in the Legal 500 as Expert Clinical...Job Title: Legal Advisor - Clinical Negligence Salary: 25k - 35k Must Haves: - Law Degree (or equivalent...

Have access to a senior clinical psychology peer group across the UK who are innovative, collaborative and promote the provision..., psychologically informed service provision and trauma-informed care and providing expert clinical consultation and professional...

for conducting a client's clinical trial Serve as a clinical expert in business presentations to new clients Qualifications.... This role will work side by side with our physicians, serving as clinical expert, to support our project teams in clinical...

planned tables, listings, and graphs Generates tables, listings, and graphs from clinical trial databases using SAS Develops... programs, verifies, validates, and maintains clinical trial databases and data entry screen using SAS and related software...

planned tables, listings, and graphs Generates tables, listings, and graphs from clinical trial databases using SAS Develops... programs, verifies, validates, and maintains clinical trial databases and data entry screen using SAS and related software...

planned tables, listings, and graphs Generates tables, listings, and graphs from clinical trial databases using SAS Develops... programs, verifies, validates, and maintains clinical trial databases and data entry screen using SAS and related software...

planned tables, listings, and graphs Generates tables, listings, and graphs from clinical trial databases using SAS Develops... programs, verifies, validates, and maintains clinical trial databases and data entry screen using SAS and related software...

planned tables, listings, and graphs Generates tables, listings, and graphs from clinical trial databases using SAS Develops... programs, verifies, validates, and maintains clinical trial databases and data entry screen using SAS and related software...

planned tables, listings, and graphs Generates tables, listings, and graphs from clinical trial databases using SAS Develops... programs, verifies, validates, and maintains clinical trial databases and data entry screen using SAS and related software...

within the Site Start-Up. Acts as country-level intelligence on start-up (SU) and clinical trial regulatory (CTR). Ensures... requirements of the clinical trial. Local Investigator Contract and Budget Negotiator - Produces site-specific contracts...

with a proven, scientific approach to complex trial data and regulatory submission challenges. Strong industry experience... Resources Information System (experience with ADP a plus) to effectively manage personnel records. Expert at organizing...

with a proven, scientific approach to complex trial data and regulatory submission challenges. Strong industry experience... Resources Information System (experience with ADP a plus) to effectively manage personnel records. Expert at organizing...