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—transforming how people think about developing new treatments so patients can access breakthrough treatments faster.

Since March 2021, we've powered 100+ clinical trials involving tens of thousands of patients.

What it's like to work here

• High-Impact, Mission-Driven Work: Disrupt an outdated industry and directly improve patients’ lives.
• Fast-Paced Growth & Ownership: Take on real responsibility across different areas.
• Collaborative, No-Ego Culture: Work with smart, driven people in a supportive, informal environment.

Role

Research Physician – provide medical expertise supporting design, execution, and monitoring of clinical research studies. Combines hands‑on medical oversight with strategic collaboration across Clinical Operations, Product, and Commercial teams.

About You

• Qualified physician with active medical registration.
• Business proficient in speaking German.
• Experience in clinical research, including trial design and execution.
• Knowledgeable in GCP, ICH guidelines, and regulatory requirements.
• Experience with medical monitoring and safety oversight in clinical trials.
• Comfortable reviewing and assessing adverse events and safety data.
• Can make informed medical decisions regarding participant safety and study continuation.
• Strong communication skills and enjoy working collaboratively across multidisciplinary teams.
• Adaptable and excited about working with technology to improve clinical trial delivery.
• Experience in a CRO, biotech or pharmaceutical setting is a plus.

Medical Oversight and Safety

• Medical monitoring and safety oversight for ongoing clinical trials.
• Review and assess adverse events, safety data, and protocol deviations.
• Medical decisions regarding participant safety and study continuation.
• Support Clinical Operations team in obtaining regulatory approvals and ensuring protocol compliance.

Trial Design and Execution

• Support design and execution of clinical trials.
• Advise on protocol development and study feasibility from a medical perspective.
• Recruit, screen and monitor safety of study participants.
• Collect clinical data according to study protocols.

Collaboration and Documentation

• Work closely with Clinical Operations, Biostatistics, Product, Data and Commercial teams.
• Maintain detailed research documentation and ensure ethical standards.
• Analyze research findings and contribute to manuscripts for publication.
• Collaborate with research coordinators and other healthcare professionals.

Strategic Support

• Support Commercial activities including bid development and bid defenses.
• Work with product team to develop and test Lindus Health's software solutions.
• Contribute medical expertise to help progress Lindus Health's strategic objectives.

What we offer

• High-impact clinical trials.
• Collaborate with industry-leading medical professionals and sponsor teams.
• Flexible scheduling and project variety.
• Competitive contractor rates.
• Established infrastructure and resources.
• Stable, well-funded organisation.
• Comprehensive support from our medical team.
• Flexibility of working as a contractor.

Hiring Process

• Interview with our Clinical Ops and Medical Talent Partner (20 mins).
• Interview with VP Medical or lead Research Physician (30 mins).

Seniority level

Mid-Senior level

Employment type

Contract

Job function

Health Care Provider

Industries

Research Services