Jr. Clinical Trials Data Specialist
TempusFull Time
Entry Level & New Grad, Junior (1 to 2 years)
Key technologies and capabilities for this role
Common questions about this position
This information is not specified in the job description.
This information is not specified in the job description.
You need 3+ years of experience developing systems and procedures to store, organise, validate and manage clinical trial data in an academic or commercial setting. Bonus experience with CDISC standards such as SDTM is also valued.
The company thrives in a startup environment that challenges the norms of typical CROs, with multidisciplinary teams including clinical and technical collaborators as well as sponsor representatives.
Strong candidates have 3+ years of clinical trial data management experience, thrive in startups, enjoy multidisciplinary teams, and bring creative thinking, attention to detail, and empathy for patients. If your experience matches some of these, they encourage you to apply.
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.