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- £39k - £51k per annumEstimated...Global Study Manager At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative...SuggestedRemote jobFlexible hours
- £56k - £72k per annumEstimated...Global Study Manager At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative...SuggestedRemote jobPermanentWork from homeFlexible hours
- £51k - £66k per annumEstimated...Remote - Sponsor Dedicated At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise... ...'s degree in health, life sciences, or other relevant fields of study. At least 10+ years of relevant experience in clinical trial management...SuggestedRemote jobFlexible hours
- £45k - £62k per annumEstimated...collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.... .... This writer will work with Peri- and Post - Approval Safety studies and RWE studies The Role Responsible for writing and reviewing...SuggestedRemote jobFlexible hours
- £54k - £71k per annumEstimated...Standards Engineer to design and implement CDISC-aligned standards and study specifications for clinical research clients. The role involves... ...IQVIA in industry forums and collaborate with CDISC-sanctioned working groups on standards development Requirements Bachelor's...Suggested
- £45k - £61k per annumEstimated...delivery of clinical trials embedded within sponsor teams. The role involves managing timelines, budgets, cross-functional teams, and study compliance across regional and global programs while leveraging IQVIA's global infrastructure and expertise. Responsibilities Lead...Suggested
- £44k - £59k per annumEstimated...direct clinical data management experience ~5+ years in a Lead Clinical Data Management role ~ Experience managing large global studies with 1,000+ patients ~ Proficiency with Medidata Rave, Oracle InForm, or similar EDC systems ~ Strong understanding of GCP, ICH,...SuggestedRemote