Posted by Parkside Office Professional • £350/day to £360/day
Clinical Trials Manager - Oncology 12 month contract Location Stockley Park (3 days onsite required) An experienced CTM with extensive oncology (preferably solid tumours) experience.
Experience in Primary Analysis and data analysis in general - Familiar with PFS and OS analysis, imaging management in oncology Clinical trials, ePRO management.
Clinical Operations is responsible for the worldwide execution of all Phase I - IV clinical trials across all therapeutic areas.
A graduate with an outstanding academic record and a personality to match is wanted to join this outstanding primary school in Harrow and Ruislip as a Graduate Teaching Assistant.
This outstanding school will appoint the right Teaching Assistant immediately to support literacy and numeracy in KS1 or KS2.
This Teaching Assistant post would suit a graduate looking work with children.
Posted by Parkside Office Professional • £50/hr to £66/hr
General
This role will be pivotal as my client evolves and transforms the facilities management function into an elevated regional business partnership, fostering holistic collaboration across all aspects of Corporate Operations.
You will transform how we operate and be a key enabler for future success by navigating and solving complex issues, delivering significant impact and value for our stakeholders in line within business imperatives.
Responsibilities include
Develop and evolve strategic relationships with site leadership teams, ensuring that business strategy and growth drivers are supported by the Corporate Operations Organisation.
Posted by US TECH SOLUTIONS LIMITED • £440/day to £450/day
General
An Exciting Contract Opportunity for Clinical Trials Manager (Oncology) with one of the Leading Biopharmaceutical Clients in UK
Description
Clinical Operations is responsible for the worldwide execution of all Phase I - IV clinical trials across all therapeutic areas.
Clinical Operations plays a key role in ensuring all clinical trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high-quality clinical data that supports global registration and commercialization of products.