Offer summary

Qualifications:

5+ years of experience in statistics/biostatistics within clinical or medical research., Extensive experience with statistical programming tools (e.g., SAS, R) and regulatory guidelines (e.g., CDISC standards)., Strong leadership abilities with experience in managing reports and mentoring teams., Exceptional written and verbal communication skills to convey complex statistical findings..

Key responsibilities:

Lead the design and implementation of statistical strategies for clinical trials across various therapeutic areas.

Oversee statistical programming efforts, ensuring high-quality analysis and reporting.

Serve as a Subject Matter Expert for statistical methodologies and provide guidance to cross-functional teams.

Communicate statistical findings effectively to both internal and external stakeholders.

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 100 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 Senior Biostatistician to input on how we design and execute statistical components of clinical trials at Lindus Health. This role is central to continually improving our Biostatistics capabilities as our customer base grows significantly over the coming years, and is our second full-time Biostatistics hire.

You’ll work closely with our Clinical Operations team and management, as well as sponsor-side teams and our Solutions and Deployment teams.

🍊About you

We’d like to hear from you if…

You bring 5+ years of experience in statistics/biostatistics within the clinical or medical research field.
You have extensive experience with statistical programming tools (e.g., SAS, R) and regulatory guidelines (e.g., CDISC standards).
You possess strong leadership abilities, with experience managing reports, leading teams or projects and providing mentorship.
You are an exceptional written and verbal communicator, with the ability to communicate complex statistical findings to diverse audiences.
You can work independently while managing multiple projects and priorities.
You are driven by a deep passion for the healthcare industry and commitment to driving innovative treatments.

🍊What you’ll focus on

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.

🍊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
Unlimited holidays; everyone is encouraged to take off at least 28 days each year
Health insurance coverage through our PEO Trinet
$40 monthly wellness allowance, which you can spend on a wellhub membership, or wellness activities and expenses of your choice!
Enhanced Parental Leave: 16 weeks full pay for primary caregiver and 6 weeks full pay for secondary caregiver
$2,000 Learning and Development allowance each year to put towards courses, certifications, and development
Regular whole company and team events, both in person and virtually.
Access to gym and retail discounts through our benefits platform Happl
Monthly lunch voucher for our remote teams
Charity events and fundraising opportunities through our charity partnership with the Forward Trust

🍊Our hiring process

Initial conversation with our Talent team (30 minutes)
Second meeting with our Biostatistics team (30 minutes)
Technical interview with Rianna (Senior Trial Manager) and Nick (Lead Biostatistician) (45 mins)
Values interview with a Cofounder and a member of the leadership team (30 minutes)
Stakeholder virtual meeting with Emma Ogburn, VP of Clinical Operations (15 minutes)

We try to arrange for at-least one interview to be in-person so you can see our office and meet more of the team.

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