Descripción de la oferta
Biorce is a pioneering Healthtech company dedicated to revolutionizing drug development through the power of AI. We are passionate about accelerating medical advancements and improving patient outcomes.
Our team comprises seasoned clinical research professionals, data scientists, and AI experts, working collaboratively to bridge the gap between cutting‑edge technology and real‑world clinical needs.
With an unwavering commitment to revolutionize healthcare, we envision a world where all patients benefit from accelerated and cost‑effective access to treatments. Biorce is poised to redefine the landscape of healthcare, shaping a future where innovation and accessibility converge for the betterment of humanity.
About the Role
Following rapid and successful global expansion, we are continuing to grow our presence in Barcelona and seeking a Product Owner to help drive our AI‑driven clinical trial solutions.
This person will play a critical role in transforming complex clinical workflows into seamless, automated tools that ensure study safety and efficiency. You will be the bridge between scientific rigor and technical execution, ensuring our squad builds the right features for the right users at the right time.
Who We’re Looking For
A detail‑oriented product specialist with a deep understanding of the clinical trial landscape. Someone who excels at translating technical and scientific data into actionable product requirements. This person should be able to take end‑to‑end accountability for a product area, making high‑impact trade‑off decisions in a fast‑paced, agile environment.
Key Responsibilities
End‑to‑End Ownership: Lead the monitoring product across all stages, from discovery and scoping through to delivery and iteration.
Backlog Management: Translate high‑level goals into a clear, prioritised backlog and actionable user stories for the engineering squad.
Cross‑Functional Alignment: Collaborate with Scientific, Engineering, and Design teams to ensure technical feasibility and operational coherence.
Requirement Refinement: Break down complex workflows—like risk detection and protocol deviation flags—into structured, simple requirements.
Performance Optimisation: Continuously improve product performance based on feedback from live studies and internal stakeholders.
Stakeholder Reference: Act as the primary product reference point for your squad, ensuring everyone understands the “what” and the “why.”
Requirements
Must-haves:
Proven experience as a Product Owner or Product Manager in SaaS or data‑heavy environments.
Deep knowledge of clinical trial processes, specifically Monitoring, RBQM/RBM, or Clinical Operations.
Expertise in breaking down complex data workflows (thresholds, KRIs, alerts) into user‑centric requirements.
Strong stakeholder management skills with the ability to simplify complex scientific topics for technical teams.
Nice‑to‑Haves:
Direct professional experience as a CRA, CTM, or in Clinical Data Management.
Familiarity with CTMS/eTMF updates and automated query generation logic.
Experience working in a high‑growth “squad‑based” agile model.
Why Join Us
A dynamic work environment with an international team, where collaboration and diversity thrive.
Work alongside top talent, united by a shared purpose and committed to making a real impact.
Comprehensive private health coverage to ensure your physical and mental well‑being.
Hybrid work model offering flexibility to balance your professional and personal life.
Company events to celebrate achievements and enjoy time together.
Get equipped with a MacBook to enhance your productivity and work experience.
Our office is pet‑friendly! You’ll likely be greeted by a few wagging tails upon arrival.
By submitting this application, I agree that my personal data will be collected, processed, and retained by the company solely for the purposes of managing and assessing my candidacy.
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