CRA (Freelance)

🍊Our mission 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. Our impact speaks for itself: 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. 🍊What's it like to work here? When you join us, you’ll experience: - High-Impact, Mission-Driven Work: Lindus is disrupting an outdated industry, giving you the chance to directly improve patients’ lives and see tangible results from your work. - Fast-Paced Growth & Ownership: We recognise hard work and outcomes over anything else. You’ll take on real responsibility, work across different areas, and actively shape the company’s success. - Collaborative, No-Ego Culture: Work with smart, driven people in a supportive and informal environment. At Lindus we break down silos, fun is a core value, and creativity is encouraged. Ready to power biology's century? We'd love to hear from you. 🍊About the role We're looking for a freelance CRA to ensure effective, risk-proportionate monitoring of Lindus Health's US portfolio of clinical trials, with immediate focus on supporting a major trial across 15+ US sites involving over 7,000 patients. Primary emphasis on remote monitoring, though some onsite visits may be required. You will undertake the preparation, conduct and reporting for all types of monitoring visits, from site selection through to close-out visits, as well as central monitoring through our Citrus platform. This freelance role is integral to maintaining high monitoring standards as our customer base grows significantly and requires someone who can work autonomously within a lean team structure, directly interfacing with Trial Managers to help shape monitoring strategy. You'll work closely with our Clinical Operations, Product and Commercial teams, as well as the sponsor-side teams that make up our customer base. 🍊About you We’d like to hear from you if… - You have 3+ years of independent site monitoring experience across all types of monitoring visits (Site selection, SIV, IMV through close-out) - You have developed strategies to effectively support remote monitoring - You have experience with Decentralized Clinical Trials (DCT) and central monitoring approaches, and are familiar with reviewing and reporting data trends and anomalies. - You can review and develop monitoring plans effectively - You understand how to take a risk-proportionate approach to monitoring and have been involved in developing monitoring plans to reflect this approach - You have a strong working knowledge of GCP/GDP and regulatory requirements. - You have a strong awareness of clinical trial regulations and are plugged in to potential changes to the regulatory environment - You have great attention to detail and are a confident communicator with internal and external stakeholders - You have a bias to action - we're looking for someone who is autonomous, proactive, organised and creative who can lead their work and report back to Trial Managers - If you've already worked in a startup or early-stage environment this will be advantageous - You're excited about helping shape clinical trial technology and don't want to work in a siloed environment You belong here! If your experience and interests match with some of the above, we want you to apply. 🍊What you’ll focus on - Focus area 1: You'll act as primary contact for end-to-end site lifecycle support, particularly for our major trial across 15+ US sites, lea...