Remote Good Clinical Practice Jobs in the UK

2 of 2 Remote Good Clinical Practice Jobs in the UK

Senior Proposals and Pricing Associate - GBR United Kingdom

United Kingdom
Hybrid / WFH Options
The Medical Research Network
Careers " Senior Proposals and Pricing Associate About MRN Medical Research Network (MRN) is an innovative market-leader of patient and site-centric solutions and clinical trial delivery. Through our integrated in-home, at-site and digital trial solutions, we allow the medical research community to create more flexible, efficient, and accessible clinical trials. We specialise in customising the … mapping of budget into client templates where required. Amendments and revision of proposals as per client and Commercial Development team requests. Liaison with internal MRN teams including Project Management, Clinical Services, Vendor Contracts Management, and others to obtain functional input for proposals and budgets for contracts and Change in Scopes. Collaborating with the Commercial Development team, Client, and Operational … the clinical research or pharmaceutical arena Prior commercial experience of sales/business development, proposal writing, or budget creation experience. Knowledge of Good Clinical Practice (GCP) and Clinical Trial Methodology (CTM) Competent user of MS Office software, advanced level MS Excel Why Join us? At MRN we offer a number of benefits designed to promote More ❯
Employment Type: Permanent
Salary: GBP Annual
Posted:

Principal Statistical Programmer

London, United Kingdom
Hybrid / WFH Options
Novartis Farmacéutica
either a large/pivotal study or several studies, or act as a Lead/Program Programmer for a small to medium sized project in phase I to IV clinical studies in Novartis Global Drug Development. Co-ordinate activities of all programmers either internally or externally assigned to the study/project work, mentor other programmers in functional expertise … effective working relationship with cross-functional teams, able to summarize and discuss status of deliverables and critical programming aspects (timelines, scope, resource plan), e.g. as member of the extended Clinical Trial Team (CTT). Review eCRF, discuss data structures and participate in data review activities as member of the extended CTT. Comply with company, department and industry standards (e.g. … including CDISC data structures as well as a solid understanding of the development and use of standard programs Good understanding of regulatory requirements relevant to Statistical Programming (e.g. GCP, study procedures). Good communications and negotiation skills, ability to work well with others globally Experience as Trial Programmer, including coordination of internal or external programmers on a given More ❯
Employment Type: Permanent
Salary: GBP Annual
Posted:
Good Clinical Practice
10th Percentile
£25,913
25th Percentile
£45,000
Median
£55,000
75th Percentile
£60,000