Role Description
We're looking for a Participant Recruitment Coordinator to join our Clinical Operations team on a freelance basis to support the growth of our team and manage participant interactions across our trials. This role requires you to be a Registered Nurse (RN) with active NMC registration.
Qualifications
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You are a Registered Nurse with current, active NMC registration (this is essential for the role).
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You have experience utilising various tech tools; bonus points if these include Calendly, DocuSign, Medi2data, Dialpad, Florence and Sealed Envelope.
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You have experience in patient onboarding and set-up, including running screening calls and patient follow-up.
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You have experience maintaining a tracking system and executing follow-up procedures.
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You have high agency and a bias for action, can adhere to protocol timelines and stay flexible in response to shifting work priorities and issues.
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You're passionate and curious about our mission: changing how the healthcare industry operates and how new health treatments are developed.
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You want to learn what life is like at a high-growth, mission-driven VC-funded startup.
Requirements
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Conduct all participant-facing tasks, ensuring a positive trial experience and excellent data accuracy within our platform, Citrus.
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Apply your clinical expertise as a Registered Nurse to support participant safety, clinical judgement and trial conduct.
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Oversee data collection and in-person processes (e.g. MRI scans), ensuring everything runs smoothly.
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Maintain and update participant trackers and the Investigator Site File (ISF).
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Assist the PI with day-to-day trial implementation and respond to CRO queries.
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Respond to any CRO data queries.
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Escalate safety, data integrity or trial operational issues to the TL/CRO team.
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Report AEs and SAEs in line with protocol and regulatory requirements.
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Collaborate effectively with trial teams to ensure seamless participant experiences throughout the trial journey.
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Contribute to team discussions by sharing participant feedback and suggesting process improvements.
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Work cross-functionally with Clin Ops, keeping the TL and STM updated at all times and ensuring other PRCs are aware of trial status.
Benefits
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High-Impact, Mission-Driven Work: Lindus is disrupting an outdated industry, giving you the chance to directly improve patientsโ lives and see tangible results from your work.
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Fast-Paced Growth & Ownership: We recognise hard work and outcomes over anything else. Youโll take on real responsibility, work across different areas, and actively shape the companyโs success.
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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.
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 donโt 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:
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Since March 2021, we've powered 100+ clinical trials involving tens of thousands of patients.
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We recently raised a $55M Series B from Balderton Capital, alongside backing from Creandum, Firstminute, Seedcamp, and Visionaries.