Company Description Architectural Standards Technical Manager Because we strive to put people first. Culture, our way. What’s a career at Primark all about? The positive impact you’re making, the experiences you’re having and the people you’re
The Clinical Data Manager performs activities pertaining to the conduct of Phase I-III clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant procedures and guidelines. The CDM ensures, from a data management perspective,
Qorvo (Nasdaq: QRVO) supplies innovative semiconductor solutions that make a better world possible. We combine product and technology leadership, systems-level expertise and global manufacturing scale to quickly solve our customers most complex technical challenges. Qorvo serves
RSL ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the
We are currently looking for an organised and motivated Paralegal to join our reputable and growing Residential Property team on a 12 month Fixed Term Contract. This is an excellent opportunity for someone looking to develop
Information & Knowledge Management Specialist Reading 6-month contract Paying up to £550p/d (Inside IR35) Please note - Due to the nature of the work, youll be required to already hold or be eligible to obtain a
SharePoint & Exchange Customer Engineer Role Overview We are seeking a highly experienced Microsoft SharePoint & Exchange Hybrid Engineer with strong enterprise-level expertise across SharePoint Online, SharePoint On-Premises, Exchange Online, and Exchange On-Premises . The candidate
We are looking for experienced Freelance Medical Writers to support an immediate requirement with a leading international organisation working within the life sciences industry. This opportunity would suit an experienced clinical/regulatory writer who has current availability
Location: United Kingdom – Fully Remote Employment Type: Full-time Industry: Clinical Research / CRO / Pharmaceutical The Opportunity We are supporting a well-established, international Contract Research Organisation (CRO) in the search for an experienced Clinical Data
Responsibilities (a) Site management • Study site selection, initiation (SIV) and clinical monitoring. • Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources