Innitius is a medical device startup developing CerviSense a CE-marked intravaginal probe that measures cervical biomechanics to support antenatal clinical decision-making across three obstetric indications: Threatened Preterm Labor Preterm Labor Screening and Induction of Labor.
We are entering our first commercial deployment phase. This is not a support role it is a founding field role that will determine whether our first clinical pilots succeed or fail.
Tasks
You will take signed hospital agreements and convert them into active high-quality clinical pilots. By December we need 710 hospitals running CerviSense in Spain and Germany with normative curve data that is clinically robust and publishable.
Lead end-to-end on-site deployment of CerviSense at each assigned hospital
Coordinate with Principal Investigators and their clinical teams to define workflows patient selection criteria and data collection procedures
Train midwives obstetricians and nursing staff; ensure consistent application technique across all operators
Troubleshoot device and application issues in real time
Ensure data quality meets the standards required for normative curve construction and peer-reviewed publication
Build clinical adoption your KPI is not installation it is that the device becomes part of the routine workflow
Provide structured field feedback to product clinical affairs and regulatory teams
Requirements
Degree in Biomedical Engineering Nursing (Clinical Specialist track) or a related health sciences discipline
25 years of experience in a clinical applications field specialist or clinical affairs role in the medical device industry
Proven ability to train clinical users and translate technical specs into practical clinical workflows
Familiarity with GCP data quality standards and MDR 2017/745Able to operate autonomously in complex hospital environments across two countries
Spanish and English required. German is a plus.
High availability for field travel across Spain and Germany
Benefits
base salary performance-based variable tied to pilot activation and data quality outcomes
First commercial deployment of a CE-marked device your work has direct clinical impact in maternal and perinatal care
Lean mission-driven team where decisions are yours to make and results are visible
Direct reporting line to the CEO
If you are someone who walks into a hospital and earns clinical credibility fast operates without hand-holding and understands that a successful deployment means adoption not just installation we want to talk.
Innitius is a medical device startup developing CerviSense a CE-marked intravaginal probe that measures cervical biomechanics to support antenatal clinical decision-making across three obstetric indications: Threatened Preterm Labor Preterm Labor Screening and Induction of Labor.We are entering our ...
Innitius is a medical device startup developing CerviSense a CE-marked intravaginal probe that measures cervical biomechanics to support antenatal clinical decision-making across three obstetric indications: Threatened Preterm Labor Preterm Labor Screening and Induction of Labor.
We are entering our first commercial deployment phase. This is not a support role it is a founding field role that will determine whether our first clinical pilots succeed or fail.
Tasks
You will take signed hospital agreements and convert them into active high-quality clinical pilots. By December we need 710 hospitals running CerviSense in Spain and Germany with normative curve data that is clinically robust and publishable.
Lead end-to-end on-site deployment of CerviSense at each assigned hospital
Coordinate with Principal Investigators and their clinical teams to define workflows patient selection criteria and data collection procedures
Train midwives obstetricians and nursing staff; ensure consistent application technique across all operators
Troubleshoot device and application issues in real time
Ensure data quality meets the standards required for normative curve construction and peer-reviewed publication
Build clinical adoption your KPI is not installation it is that the device becomes part of the routine workflow
Provide structured field feedback to product clinical affairs and regulatory teams
Requirements
Degree in Biomedical Engineering Nursing (Clinical Specialist track) or a related health sciences discipline
25 years of experience in a clinical applications field specialist or clinical affairs role in the medical device industry
Proven ability to train clinical users and translate technical specs into practical clinical workflows
Familiarity with GCP data quality standards and MDR 2017/745Able to operate autonomously in complex hospital environments across two countries
Spanish and English required. German is a plus.
High availability for field travel across Spain and Germany
Benefits
base salary performance-based variable tied to pilot activation and data quality outcomes
First commercial deployment of a CE-marked device your work has direct clinical impact in maternal and perinatal care
Lean mission-driven team where decisions are yours to make and results are visible
Direct reporting line to the CEO
If you are someone who walks into a hospital and earns clinical credibility fast operates without hand-holding and understands that a successful deployment means adoption not just installation we want to talk.