Lindus

We are an equal opportunity employer committed to building a diverse and inclusive workforce. We evaluate all candidates based solely on their skills, experience, and qualifications relevant to the role. We do not discriminate on the basis of race, ethnicity, religion, gender, gender identity, sexual orientation, age, disability, veteran status, or any other legally protected status.

Configuration Specialist

Location

United States

Posted

75 days ago

Salary

0

Seniority

Mid Level

No structured requirement data.

Job Description

Configuration Specialist

Lindus

Role Description We're looking for a Configuration Specialist to help us accelerate our mission to power biology's century with radically faster, more reliable clinical trials. This is a hands-on technical role within our Deployment function, the team responsible for building and delivering clinical trials on Citrus, our proprietary platform. You will own the setup and testing of studies, working from detailed design specifications to produce something that works reliably for the people running and participating in the trial. No two studies are the same, and the work you do directly affects how quickly a trial gets off the ground and how reliably it runs. Qualifications - You have a technical background, whether through a degree in a relevant field or hands-on experience in software, data, or systems work. - You are comfortable working from detailed specifications and have a clear instinct for when to get on with it and when to ask. - You are precise and thorough by nature, and comfortable maintaining that standard in a fast-moving environment. - You keep track of multiple things at once without things falling through the cracks. - You have some experience in a regulated or quality-focused environment, whether in healthcare, finance, or elsewhere. Requirements - Setting up studies on Citrus based on approved specifications, covering data collection forms, participant schedules, logic rules, and user access. - Running automated checks to make sure everything in the build matches what was agreed before a study goes live. - Coordinating testing with internal teams and sponsors, writing test scripts, working through issues, and making sure everything is resolved before sign-off. - Making approved changes to live studies and keeping things accurate and compliant as trials evolve. - Coordinating go-live activities and confirming everything is running correctly before a study is declared live. Benefits - Competitive salary plus meaningful equity - you'll own a piece of what we're building. - $2,000 annual Learning & Development budget for courses, certifications, and conferences. - 39 days annual leave (27 days PTO + 11 federal holidays + 1 James Lind Day). - $800 monthly employer contribution for insurance coverage (via Trinet PEO). - $40 monthly wellness allowance with flexibility on how to spend this, including opting in to a company private health insurance or wellhub membership. - Access to gym and retail discounts through Happl. - Monthly lunch vouchers for remote team members. - Regular company events and team gatherings (both virtual and in-person). - Charity partnerships and volunteering opportunities with Forward Trust. - Work with a team that's genuinely changing healthcare for the better. Company Description We're powering biology's century with radically faster, more reliable clinical trials. Every new treatment needs clinical trials to prove safety and efficacy, but today's infrastructure is stuck in the past - driving up cost, causing delays and ultimately meaning new treatments don’t get to patients. We're fundamentally changing that - not just being a "better CRO," but transforming how people think about developing new treatments, so patients can access breakthrough treatments faster. - Since March 2021, we've powered 100+ clinical trials involving tens of thousands of patients. - We recently raised a $55M Series B from Balderton Capital, alongside backing from Creandum, Firstminute, Seedcamp, and Visionaries.

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