Senior Data Manager

🍊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• High-Impact, Mission-Driven Work: Lindus is disrupting an outdated industry, giving you the chance to directly improve patients’ lives and see tangible results from your work.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

Lindus Health is looking for a Senior Data Manager who treats data management as a technical discipline, one that can be executed with precision, consistency and a genuine commitment to quality. You will own a portfolio of concurrent trials end-to-end, taking full responsibility for data quality from first patient visit through database lock. You will write scripts where manual review would otherwise slow things down, and build repeatable workflows in place of one-off reports. You will be the primary sponsor-facing contact for data management planning and data quality, and will work closely with study teams to ensure data quality requirements are reflected throughout.

This is a unique opportunity for someone with extensive data management expertise at a tech-enabled Clinical Research Organization. You will contribute operational feedback that helps shape how data management within our end-to-end trial delivery platform, Citrus, evolves.

🍊 About you

We would like to hear from you if...

• You have 5+ years of clinical data management experience, including at least 2 years leading studies independently through lock

• You have deep hands-on experience with EDC platforms and can review build specifications and edit check logic with a critical eye; you understand how build decisions affect downstream data quality

• You are comfortable working with data programmatically; experience with scripting languages such as Python, R, or SQL is a plus, and you are expected to develop these skills on the job

• You have working knowledge of CDISC standards, particularly CDASH; SDTM familiarity is valued

• You have experience with external data transfers and reconciliation across multiple data sources

• You have strong working knowledge of GCP, ICH E6, and 21 CFR Part 11

• You have direct sponsor-facing experience and are comfortable owning that relationship independently

• You thrive in a startup environment that challenges the norms of typical CROs

• You have high agency and a bias for action

• You are passionate about our mission: changing how the healthcare industry operates and how new health treatments are developed

🍊 What you'll focus on

• Own assigned studies end to end, including defining critical data items, the data management plan, query lifecycle, external data reconciliation, and database lock

• Manage the full query lifecycle from generation through resolution, working directly with sites and sponsor data teams

• Lead proactive data review to ensure key study milestones remain on target

• Review build specifications to ensure they yield high-quality data capture on assigned studies, including edit check logic

• Participate in UAT, ensuring the study build meets the requirements of the protocol prior to go-live

• Perform ongoing safety data review and facilitate medical coding (MedDRA, WHODrug) in collaboration with the medical team

• Build sponsor-facing reports using programmatic data access (e.g., Python, R, SQL), interpreting data trends and tailoring outputs to sponsor expectations

• Serve as the primary DM contact for sponsors on assigned studies, managing the relationship and data communications independently; escalate to the AD DM when needed

• Conduct all data management activities in accordance with relevant regulations and Lindus SOPs

• Maintain study documentation to a standard that holds up under audit or inspection

• Flag SOP gaps encountered during study execution and contribute to revisions when asked

• Provide structured feedback on platform limitations that affect data quality or site burden, and translate operational experience into actionable input for the product team

• Share learnings with peers and newer team members through the work

We will only contact you from lindushealth.com email addresses. Please check the spelling of emails which appear to come from Lindus 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