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Quality Control Specialist Location: HertfordshireJob Type: PermanentSalary: Competitive against the current marketCompany: Cell and Gene Therapy Over
Senior Regulatory Associate; Specialist Pharma; EU focus; Post Marketing changes; North West London
Regulatory Affairs Team Leader - Life-cycle Change Management; Specialist Pharma; North West London; EU & some International; Team & Project Manage
At Lonza, we invest in great people. We encourage our employees to challenge themselves and we offer an environment that fosters creativity and
Regulatory Affairs Change Lead: Post approval; Project Manage; Specialist Pharma; North West London
Statistical Team Leader (home or office based), leading CRO, work with statisticians, programmers, DM and project team to provide statistical insight
Senior Statistical Programmer for a world leading pharmaceutical company offering excellent career opportunities and generous benefits.
Health Economics Specialist UCB – Inspired by patients. Driven by science Help us transform patients’ lives About UCB At UCB, we put our heart, sou...
Associate Director Statistics, leading pharmaceutical company, provide support for design, analysis, interpretation, and reporting of data evidence.
Study Lead Clinical Data Managers, global CRO, Oncology and RAVE experience an advantage, leadership skills, project planning, execution and close-out
Recruitment Specialist (preferably with a pharma background recruiting Statisticians, SAS Programmers or Data Managers/Data Scientists)
Our client is currently looking for an Account Manager / Senior Account Manager to join their team in Healthcare PR team in London. They are an awa...
Our client is a successful healthcare communications agency who are looking for an experienced Account Director to join their team in London. They...
Our client is a successful independent medcomms agency based in Cheshire and in need of an Editorial Manager to lead their medical writing team.
Our client is an award winning medcomms agency seeking an experienced Senior Medical Writer to join their team.
Our client is one of the market leaders in global medical communications and seeking a Principal Medical Writer for their team in London or Cheshire.
Our client is a full-service medcomms agency seeking a Principal Medical Writer to join their team in London, Cheshire or Basel.
PPD are looking for Safety Administrator to join our growing Budget Operations team.The successful candidate will enter data into our internal/externa
PPD is a leading global contract research organization providing drug discovery, development and lifecycle management services. Our clients and partne
An opportunity to work with A Global leading Clinically focused company who support and train their CRA's to be promoted to new opportnuities.