Jobs at Djinni

Binariks is looking for an experienced Subject Matter Expert / Product Manager with deep domain knowledge in clinical data and regulatory standards (eCRF, CDISC SDTM) to embed directly within the client's product organization. Working under the supervision of a Senior or Lead Product Manager, you will help translate complex clinical and regulatory requirements into clear, actionable product specifications for specific features of a research software platform.
Our client develops secure, standards-compliant digital health solutions that empower researchers and public health institutions to advance evidence-based medicine. The company builds scalable research infrastructures, supports international standards such as FHIR, OMOP, and CDISC, and collaborates with some of the world’s leading clinical institutions.


What We’re Looking For:
 

• 5+ years of experience as a Product Owner / Product Manager / Clinical Product Specialist, ideally in clinical research, EDC/eCRF, CTMS, or healthcare data platforms
• Hands-on experience with eCRF design (form definition, edit checks, CRF lifecycle, study build) using EDC platforms such as Medidata Rave, Veeva Vault CDMS, OpenClinica, REDCap, Castor, or equivalent
• Solid working knowledge of CDISC SDTM (and ideally CDASH, ADaM, Define-XML, ODM-XML) and how clinical data flows from collection to submission
• Familiarity with clinical research operations: protocols, study lifecycle, data management plans, monitoring, and the role of CROs and sponsors
• Strong understanding of regulatory and quality frameworks relevant to clinical data: GCP/ICH E6, 21 CFR Part 11, GDPR/HIPAA, with awareness of EMA/FDA submission expectations
• Experience with Agile development methodologies and tools (Jira, Confluence, etc.)
• Excellent communication and stakeholder management skills, with the ability to bridge technical and clinical/regulatory audiences
• Professional written and spoken English
  
   

Your Responsibilities:
 

• Act as the domain expert on clinical data capture and regulatory data standards — bringing eCRF design experience and a working knowledge of CDISC SDTM (and ideally CDASH, ADaM, ODM-XML) into product discussions
• Prepare detailed product requirements, user stories, and acceptance criteria for specific features, working under the supervision of the Senior / Lead Product Manager
• Translate complex clinical and regulatory standards into product specifications that engineering, design, and data teams can implement with confidence
• Manage and groom the backlog for the assigned feature areas, ensuring alignment with the broader product roadmap and strategic objectives set by the Lead Product Manager
• Facilitate sprint planning, backlog refinement, and release cycles using Agile methodologies.
• Collaborate with clinical researchers, study managers, data managers, and biostatisticians to gather requirements, validate prototypes, and refine workflows
• Ensure features meet regulatory expectations (GDPR, HIPAA, GCP/ICH E6, 21 CFR Part 11 where applicable) and support seamless data standardization, traceability, and interoperability
• Define and monitor product metrics for the assigned feature areas, providing regular updates to stakeholders

Would be a plus
 

• Bachelor's or Master's degree in Life Sciences, Health Informatics, Biostatistics, Computer Science, Bioinformatics, or a related field
• Spoken and written German
  
   

Binariks is looking for an experienced Senior Mobile Engineer (React Native) to embed directly within one of the client's existing product teams. You will work side by side with in-house engineers, designers, QA specialists, and product managers to ship features that bring research-grade digital health products into the hands of patients, clinicians, and study participants.
Our client develops secure, standards-compliant digital health solutions that empower researchers and public health institutions to advance evidence-based medicine. The company builds scalable research infrastructures, supports international standards such as FHIR, OMOP, and CDISC, and collaborates with some of the world’s leading clinical institutions.

What We’re Looking For:
 

• 5+ years of professional experience as a mobile or frontend engineer, with at least 2+ years hands-on with React Native in production
• Proven experience shipping native or cross-platform mobile apps on Android (iOS experience is a strong plus)
• Solid command of TypeScript / JavaScript, HTML, and CSS, plus the React ecosystem (hooks, modern state management, navigation libraries)
• Experience integrating native modules and bridging to platform APIs; familiarity with Bluetooth Low Energy or device/wearable SDKs is highly desirable
• Strong focus on performance, semantic markup, accessibility, and security
• Experience with mobile testing (unit, component, end-to-end) and CI/CD pipelines for mobile releases (Fastlane, App Store / Play Store distribution)
• Experience in Healthcare projects (knowledge of GDPR, HIPAA)
• Professional written and spoken English

Your Responsibilities:
 

• Build and ship state-of-the-art mobile features in React Native — writing accessible, performant, maintainable, and well-tested code following clean-code principles
• Develop, test, and review code; contribute to mobile architecture, navigation, state management, and offline-first patterns
• Implement modules that connect to wearable sensors and devices via Bluetooth Low Energy (BLE) and via the SDKs of mobile phones, smart watches, and other wearables
• Contribute to the existing Wear OS companion app (Kotlin) where collaboration with the mobile team requires it
• Apply strong UI craftsmanship to deliver digital health products and prototypes that meet our quality and accessibility standards
• Engage with security, privacy, and regulatory requirements (GDPR, HIPAA) when handling patient or study data on the device
• Collaborate closely with UX Design, Backend Engineering, QA, and Product Management as part of an integrated team

Would be a plus

• Experience with Kotlin and Wear OS / Android Wearable APIs
• Exposure to digital health, clinical research, or regulated environments
• Familiarity with healthcare data standards (FHIR, OMOP) and patient-data privacy obligations
• Experience working in a staff-augmentation or embedded-consultant model
• University degree in Computer Science, Software Engineering, or a related field, or equivalent professional experience
• Spoken and written German