🍊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 $18m Series A round from some great investors including Creandum, Peter Thiel and Firstminute to power the next stage of our growth.
🍊About the role
We’re looking for someone experienced in implementing the full trial life cycle for multi-site and/or decentralized trials, who can bring a creative and proportionate approach to trial creation and delivery.
The ideal candidate will have a deep understanding of regulations including ICH GCP and FDA/EMA/MHRA regulatory requirements to help ensure best practice and to successfully lead, train and support trial teams. Experience across a variety of disease areas of Phase I-IV trials, complex trial designs, interventional, medical device and drug trials experience is essential. This is a pivotal role as you will also be supporting the scale-up of our clinical operations team. You will also support our Product and Solutions teams in enhancing our product and winning new business.
You will work closely with the US Director of Clinical Operations, the VP of Clinical Operations, the Associate Director(s) of Study Management and the global Clinical Operations team. We are also hiring for this role in the US.
🍊About you
10+ years experience in Clinical Operations, implementing and successfully delivering trials
Good experience and understanding of ICH GCP and FDA/EMA/MHRA regulatory requirements
Experienced team leader
Previous startup/biotech experience is a plus
Understands commercial aspect so has experience of collaborating with Sponsors, vendors and business development
Experience of creating and implementing regulatory compliant proportionate processes
You have high agency and a bias for action
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
Project Leadership and Delivery
Oversee the day to day running of clinical trial programs and projects, ensuring that they deliver successfully (i.e., conduct trials on time, on budget, in compliance, and of high quality)
Advise on development of Study Management scope and activities to improve efficiency and enable robust interfaces and/or execution.
Create and maintain optimal working practices, SOPs, systems and tools, to ensure robust Study Management execution and stakeholder communications.
Where necessary ensure project continuity through key transition events and staff absences
Coordinate activities and deliverables of all project conduct and proactively identify and manage issues
Reporting and Communication
Responsible for project management components of inspection readiness for all aspects of the project conduct, including Trial Master Files
Provide oversight for development and implementation of project plans in accordance with Lindus Health Controlled Documents
Independently prepare, coordinate, and present project material at internal and external meetings
Direct the activities of assigned Project Support staff and mentor other project management team members and clinical staff; facilitate team building and communication
Implement resource strategies to achieve project goals
Develop contingency planning and risk mitigation strategies to ensure successful delivery of project goals
Training
Business Development
Product
Work closely with the tech and product teams to help design best-in-class trial technology that exceeds customer demands (e.g., EDC, e-Consent, eTMF)
Collaborate to develop formal study requirements that enable rigorous validation of clinical trial software, and contribute to the development and maintenance of our SOPs and policies
🍊What we offer
Make an impact across all areas of our business and fix one of the world’s most broken industries
Competitive salary, plus meaningful stock options
Flexible working - You will be based out of our London office and we encourage you to spend at least 60% of your time per month (averaging 3 days a week) in the office and the remaining time at home.
Unlimited holidays; everyone is encouraged to take off at least 28 days each year
Health & wellbeing - cashback scheme with Medicash (unlimited virtual GP appointments, medical, dental, optician, physio, mental health + more!)
Gympass membership; flexible access to gyms, studios, classes and wellness apps
Enhanced Parental Leave - 12 weeks full pay for primary care giver & 4 weeks full pay for secondary care giver
Cycle to work scheme
Regular team events; recently we’ve been to Legoland, a Bake Off competition, and a Millwall FC home game (decided by popular vote)
Up to ÂŁ1,000 per year towards courses, certifications and development
A new laptop as your main workstation and up to ÂŁ500 towards setting up your home office
🍊Our hiring process
Initial interview with our Director of Talent to present the company mission and vision and answer any of your questions.
Initial interview with the VP of Clinical Operations (30 minutes)
Technical interview with VP of Clinical Operations and a member of the Clinical Operations team (60 minutes)
Values interview with 2 members of the Founding team (60 minutes)
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