Lindus Health

• Conduct all participant facing tasks, ensuring a positive trial experience and excellent data accuracy within our platform, Citrus • Oversee data collection and in-person processes (e.g. MRI scans) are conducted smoothly • Maintain and update participant trackers and Investigator Site File (ISF) • Assist PI with day-to-day trial implementation and respond to CRO queries • Respond to any CRO data queries • Escalate safety, data integrity or trial operational issues to the TL/CRO team • Reporting AEs and SAEs • Collaborate effectively with trial teams to ensure seamless participant experiences throughout the trial journey • Contribute to team discussions by sharing participant feedback and suggesting process improvements • Cross Functional working with Clin Ops - keeping TL and STM updated at all times and other PRCs aware of trial status

• Lead on GCP quality across the business: audit programme design and execution, inspection readiness, and ongoing compliance with ICH GCP and applicable regulations (UK, EU, US) • Provide hands-on GCP auditing of trials, sites, vendors, and internal processes - working with clinical operations teams to identify risks and drive corrective actions • Prepare staff and trial materials for external sponsor audits and regulatory inspections, supporting the team through the process and any required follow-up • Assess and advise on potential serious breaches, protocol deviations, and GCP quality issues, ensuring appropriate reporting and resolution • Keep current with evolving regulations and guidance, translating these into practical updates for the clinical operations and quality teams • Provide ad-hoc US regulatory and FDA-specific good practice guidance as our US trial portfolio expands • Maintain overall oversight of the Integrated Management System (IMS), working with the Business Quality Manager to ensure ISO 9001 and ISO 27001 processes are implemented and continuously improved • Ensure quality documentation - SOPs, policies, risk assessments - is accurate, current, and practical for the teams using it • Oversee deviation, CAPA, and vendor management processes across the business • Review clinical operations study documents in development to ensure compliance with current clinical trial regulations • Collaborate with our external GCP support partners (audit consultancies, regulatory advisors) to supplement in-house capability where needed • Line manage the Business Quality Manager and GCP Quality Associate, ensuring both streams of quality work are resourced, prioritised, and delivering value • Build strong working relationships with clinical operations leadership (US and UK), product/engineering, and commercial teams - quality needs to be embedded, not siloed • Contribute to the wider operations leadership team on quality strategy, risk, and compliance matters

• Lead on GCP quality across the business: audit programme design and execution, inspection readiness, and ongoing compliance with ICH GCP • Provide hands-on GCP auditing of trials, sites, vendors, and internal processes - working with clinical operations teams to identify risks and drive corrective actions • Prepare staff and trial materials for external sponsor audits and regulatory inspections, supporting the team through the process and any required follow-up • Assess and advise on potential serious breaches, protocol deviations, and GCP quality issues • Keep current with evolving regulations and guidance • Provide ad-hoc US regulatory and FDA-specific good practice guidance as our US trial portfolio expands • Maintain overall oversight of the Integrated Management System (IMS) • Ensure quality documentation - SOPs, policies, risk assessments - is accurate, current, and practical for the teams using it • Line manage the Business Quality Manager and GCP Quality Associate, ensuring both streams of quality work are resourced, prioritised, and delivering value

• Lead our UK & EU Clinical Operations team • Responsible for our portfolio of trials and scaling our UK & EU operations • Use AI tools to reshape and improve clinical operations, trial oversight and trial delivery • Input on the roadmap and features of our proprietary trial technology platform, Citrus • Oversee the UK & EU Clinical Operations team, ensuring that trials are delivered successfully (on time, on budget, in compliance, and of high quality) • Create and maintain optimal working practices, SOPs, systems and tools for robust Study Management execution and stakeholder communications • Work with Clinical Operations leadership to proactively solve issues • Direct Project Support staff and mentor project management and clinical staff; facilitate team building and communication • Implement resource strategies to achieve project goals • Develop contingency planning and risk mitigation strategies • Lead hiring and expansion of the UK & EU ClinOps team • Develop and deliver team training reflective of current best practice • Ensure seamless integration of our US Clinical Operations team

🍊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 Health 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 CRA to ensure effective, risk-proportionate monitoring of Lindus Health's global 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 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, COV) - 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 - You're comfortable with up to 60% travel during busy periods - Ideally based in the Central Time Zone near a major airport hub - Have a full US driving licence - 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, leading effective monitoring according to trial protocols, including writing Monitoring Plans, arranging and conducting site monitoring visits (primarily remote) and creating monitoring reports for all visit types from SIV to close-out. - Focus area 2: You'll coordinate and lead monitoring activities and deliverables autonomously, identifying and managing issues while proactively advising Trial Managers on improvements to our processes. You may also be pulled onto other trials as business needs require. - Focus area 3: You'll work closely with our tech and product teams to help design and shape our best-in-class Citrus trial monitoring platform, providing direct input that exceeds customer demands. 🍊What we offer (US) This is a 6 months fixed term contract position - 20 days holiday allowance per annum (pro rataʼd to length of contract) - $800 monthly health insurance contribution - Enhanced Parental Leave - 16 weeks at full pay for primary caregivers and 6 weeks at full pay for secondary caregivers (at 1 year of employment) - Please note you will not be required to join company off sites or company wide meetings in this role. 🍊Our hiring process We believe hiring should be transparent, respectful of your time, and give you a real feel for what Lindus Health is like. Here's what to expect: - Online Logical Reasoning and Problem Solving test (15 minutes) - Initial conversation with Heather, our ClinOps Talent Partner (30 minutes) Get to know each other, discuss the role, and answer any questions about Lindus - Second conversation with one of our Clinical Monitoring Manager (30 minutes) Deep dive into your experience and how you'd approach key challenges - Technical/functional interview with an AD of ClinOps and a member of our CRA team(45 minutes) This will include a task you’ll need to prepare in advance of the interview and talk to - Values interview with 2 team members of leadership (30 minutes) A chance to get to know each other and explore how our values align We will only contact you from lindushealth.com email addresses. Please check the spelling of emails which appear to come from Lindus Health carefully before responding. We will never ask for your financial information over email. 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

• Lead Statistical Strategy Design: Take ownership of statistical strategy and analysis for clinical trials across multiple therapeutic areas and phases. Create and implement statistical Standard Operating Procedures. Collaborate closely with sponsors and the wider clin ops teams to ensure tailored solutions. • Advanced Statistical Programming and Analysis: Lead statistical programming efforts for complex clinical trials, ensuring high-quality analysis and reporting. • Cross-Functional Leadership: Serve as an internal Subject Matter Expert (SME) for statistical methodologies, trial design, and data management. Provide guidance to cross-functional teams, including Clinical Operations and Data Management, and external stakeholders. • Line Management and Mentorship: Take responsibility for line managing and/or mentoring junior team members. Help develop internal processes and best practices to ensure high quality results as our customer base grows. • Stakeholder Communication: Communicate statistical findings effectively to both internal and external stakeholders, ensuring clarity and understanding across both technical and non-technical audiences.

🍊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 Health 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. Job Description 🍊Our mission All new medicines need to undergo clinical trials to show they’re safe and effective. But today’s clinical trial infrastructure is stuck in the past, and the cost of developing new medicines has skyrocketed as a result. Patients have to wait longer and pay more for new treatments. Our mission is to fix this; we use software to help innovative companies run faster, more reliable, and patient-friendly clinical trials. We’re still a young company, but we’ve already had a big impact. Since founding the company in March 2021 we’ve helped run over 80 clinical trials involving tens of thousands of patients, with a customer NPS of 100. We recently raised a $55m Series B round from Balderton Capital, with support from Creandum, Firstminute, Seedcamp, and Visionaries. 🍊About the role We’re looking for a Participant Recruitment Coordinator to join our Clinical Operations team on a Fixed Term Contract to support the growth of our team and manage the participant interactions of our trials. 🍊About you We’d like to hear from you if… - You have experience in utilizing various tech tools; bonus if these include Calendly, Docusign, Medi2data, Dial Pad, Florence and Sealed Envelope - You have experience in patient onboarding and set up; including running screening calls and patient follow up - You have experience of maintaining a tracking system and executing follow-up procedures - You have high agency and a bias for action and are able to adhere to protocol timelines and able to be flexible in response to work priorities and issues - You are passionate and curious about our mission; changing how the healthcare industry operates and how new health treatments are developed - You want to learn what life is like at a high-growth, mission-driven VC funded startup You belong here! If your experience and interests match with some of the above, we want you to apply. 🍊What you’ll focus on - Conduct all participant facing tasks, ensuring a positive trial experience and excellent data accuracy within our platform, Citrus - Oversee data collection and in-person processes (e.g. MRI scans) are conducted smoothly - Maintain and update participant trackers and Investigator Site File (ISF) - Assist PI with day-to-day trial implementation and respond to CRO queries - Respond to any CRO data queries - Escalate safety, data integrity or trial operational issues to the TL/CRO team - Reporting AEs and SAEs - Collaborate effectively with trial teams to ensure seamless participant experiences throughout the trial journey - Contribute to team discussions by sharing participant feedback and suggesting process improvements - Cross Functional working with Clin Ops - keeping TL and STM updated at all times and other PRCs aware of trial status 🍊What we offer (US) - 20 days holiday allowance per annum (pro rataʼd to length of contract) - $800 monthly health insurance contribution - Enhanced Parental Leave - 16 weeks at full pay for primary caregivers and 6 weeks at full pay for secondary caregivers (at 1 year of employment) - Please note you will not be required to join company off sites or company wide meetings in this role. 🍊Our hiring process We believe hiring should be transparent, respectful of your time, and give you a real feel for what Lindus Health is like. Here's what to expect: - Online Logical Reasoning and Problem Solving test (20 minutes) - Initial conversation with our ClinOps Talent Partner (15 minutes) Get to know each other, discuss the role, and answer any questions about Lindus - Technical/functional interview with two members of our Clinical Operations team (45 minutes) This will include a task you’ll need to prepare in advance of the interview and talk to - Values interview with 2 team members of leadership (30 minutes) A chance to get to know each other and explore how our values align We will only contact you from lindushealth.com email addresses. Please check the spelling of emails which appear to come from Lindus Health carefully before responding. We will never ask for your financial information over email. 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

🍊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 Health 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 dynamic Sub-Investigator to support a live US clinical trial while serving as an active advocate and advisor for Lindus Health. This is an immediate need for an active study, combining hands-on protocol execution with strategic advisory contributions to help position Lindus Health competitively in the US market. Unlike traditional Sub-Investigator positions, this role requires someone who can articulate and champion Lindus Health's innovative approach to clinical trials, contribute meaningfully to bid proposals and client presentations and serve as a credible voice for our capabilities in the market. 🍊About you We’d like to hear from you if… - You are a board-certified psychiatrist or physician with substantial psychiatry clinical trial experience. You must hold a current, unrestricted medical license (MD, DO, or equivalent) in at least one of the following states: Ohio, Georgia, Michigan, New Jersey, Washington, Massachusetts, Indiana, Maryland, Missouri, Wisconsin, or Colorado. - You're GCP-certified with demonstrated clinical research experience and understanding of ICH-GCP guidelines and FDA regulations - You're a dynamic communicator who can credibly champion Lindus Health's approach in client-facing situations - You're responsive, engaged, and bring strategic insights beyond basic protocol execution - You're business-minded with genuine enthusiasm for clinical research innovation You belong here! If your experience and interests match with some of the above, we want you to apply. 🍊What you’ll focus on - Champion Lindus Health: Actively participate in bid proposals, represent our values in client-facing situations, and help us win business with your clinical credibility and advocacy - Provide medical oversight: Conduct clinical research activities in accordance with GCP guidelines, supervise investigational product testing, and ensure informed consent and protocol compliance - Ensure participant safety: Monitor and promptly report adverse events, protocol deviations, and any safety concerns throughout all phases of the trial - Manage study documentation: Complete case report forms accurately and timely through our Citrus platform, maintain comprehensive study records, and ensure proper investigational product handling - Collaborate across teams: Work closely with Clinical Operations, Product, and Commercial teams while responding promptly to all information requests and maintaining transparent communication 🍊 What we offer Make an impact across all areas of our business and fix one of the world’s most broken industries. - Work on high-impact clinical trials - Collaborate with industry-leading medical professionals and sponsor teams - Enjoy flexible scheduling and project variety - Competitive contractor rates - Leverage our established infrastructure and resources - Work with a stable, well-funded organisation - Contribute your expertise to meaningful research - Receive comprehensive support from our medical team - The flexibility of working as a contractor 🍊Our hiring process - Initial conversation with Cam, our Medical Talent Partner (20 minutes) - Technical interview with Luke, our VP of Medical (30 minutes) We will only contact you from lindushealth.com email addresses. Please check the spelling of emails which appear to come from Lindus Health carefully before responding. We will never ask for your financial information over email. 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

🍊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 Health 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 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. 🍊 About you We'd like to hear from you if... - 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 You belong here! If your experience and interests match with some of the above, we want you to apply. 🍊 What you'll focus on - 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 🍊What We Offer (US) We believe in rewarding the people who are building the future of clinical research. Financial & Growth: - 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) Health & Wellbeing: - $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 Culture & Connection: - 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 🍊Our Hiring Process We believe hiring should be transparent, respectful of your time, and give you a real feel for what Lindus Health is like. Here's what to expect: Criteria a 15 minute critical thinking and problem solving test Introduction with Sophie, Talent Lead (30 mins) Get to know each other, discuss the role, and answer any questions about Lindus Expertise interview with Elaine AD deployment (30 minutes) Technical interview with with a Solutions Architect (Connor, Tatiana, or Shreya) and a Solutions Engineer (Fabiha, Roman, Sara or Nate) (60 minutes) Values interview with a co-founder and Veronica VP Deployment (30 mins) - A chance to get to know each other and explore how our values align We will only contact you from lindushealth.com email addresses. Please check the spelling of emails which appear to come from Lindus Health carefully before responding. We will never ask for your financial information over email. 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

• Oversee a portfolio of 3-5 active trials, supporting Project Leads to ensure trial success through effective resourcing, timeline management, and strategic guidance. • Manage commercial matters within agreed SOW parameters, own sponsor account relationships, and play a pivotal role in the handover of projects from Business Development to Clinical Operations. • Shape working practices, develop SOPs, lead training programs, and serve as an escalation point for complex trial challenges. • Ensure effective oversight of trial delivery and maintain high standards across the portfolio.