Clinical Research Associate
Abarca Health- Full Time
- Junior (1 to 2 years)
Candidates should have 3+ years of work experience in a clinical trial monitoring role, including monitoring at NHS sites, and a strong awareness of clinical trial regulations. They should also understand how to take a risk-proportionate approach to monitoring and have been involved in developing monitoring plans, along with a full UK driving license. Previous involvement in US trials would be beneficial.
The Clinical Research Associate will ensure effective risk-proportionate monitoring of Lindus Health’s global portfolio of clinical trials, which involves both central and onsite monitoring, potentially including travel to sites across the UK. They will prepare, conduct, and report on trial monitoring visits, reviewing data in real-time via the Citrus platform and collaborating closely with Clinical Operations, Product, and Commercial teams, as well as sponsor-side teams to maintain high monitoring standards and support customer base growth.
Accelerates clinical trials for life sciences
Lindus Health focuses on speeding up clinical trials to help patients access new treatments more quickly. The company operates differently from traditional contract research organizations (CROs) by using a fixed-price model for studies and milestone-based payments, which aligns their incentives with those of their clients. Lindus Health combines a skilled clinical operations team with a specialized software platform and access to a vast database of 30 million Electronic Health Records. They handle all aspects of clinical studies, including designing the study, recruiting patients, capturing clinical data, monitoring progress, and managing projects. With their approach, Lindus Health has successfully assisted over 90 sponsors in conducting clinical trials across the US, UK, and Europe, completing them up to three times faster than conventional CROs and often delivering results ahead of schedule.