Offer summary

Qualifications:

2+ years of experience in statistics or biostatistics, preferably in the medical or clinical research field., Proficiency in statistical programming tools such as STATA or R., Knowledge of regulatory guidelines and CDISC standards is preferred., Strong written and verbal communication skills to explain statistical concepts to non-statisticians..

Key responsibilities:

Assist in developing statistical methods and analysis plans for clinical trials across various therapeutic areas and phases.

Perform statistical programming tasks for the conduct and reporting of clinical trials.

Collaborate with Clinical Operations, Data Management, and other internal teams to provide statistical expertise for trial design and execution.

Communicate complex statistical results clearly to both technical and non-technical 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 are seeking a Biostatistician to join our growing team, offering an exciting opportunity for someone with at least 2 years of experience in statistics or biostatistics within the medical or clinical field. As a key member of our team, you’ll work closely with cross-functional groups to design and implement statistical methods and programming for clinical trials, while gaining valuable exposure to cutting-edge technologies in healthcare.

🍊About you

We’d like to hear from you if…

You bring 2+ years of experience in statistics/biostatistics, preferably within the medical or clinical research field.
You have experience with statistical programming tools (e.g., STATA, R).
You possess knowledge of regulatory guidelines and CDISC standards (preferred).
You are a strong written and verbal communicator with an ability to explain statistical concepts to non-statisticians.
You can work independently, manage your own workload, and stay organised.
You are driven by a passion for healthcare innovation and the mission of changing how the industry operates and develops new treatments.

🍊What you’ll focus on

Statistical Strategy Design: Assist in developing statistical methods and analysis plans for clinical trials across a variety of therapeutic areas and phases, working closely with trial teams, biostatistics leadership and sponsors.
Statistical Programming and Analysis: Perform statistical programming tasks for the conduct and reporting of clinical trials
Cross-Functional Collaboration: Work with Clinical Operations, Data Management, and other internal teams to provide statistical expertise and support for clinical trial design and execution.
Communication and Reporting: Communicate complex statistical results in a clear and understandable manner to both technical and non-technical stakeholders.

🍊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 Emma (VP ClinOps), Rianna (Senior Trial Manager) and Nick (Lead Biostatistician) (45 mins)
Values interview with 2 members of the Executive Team (30 minutes)
Stakeholder virtual meeting with Emma Ogbrun, 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.

Required profile