Field Clinical Specialist provides education, training, and clinical support for Inari products in hospital settings, collaborating with account managers and medical teams.
Compensation
Base/Draw + commission: $130,000 and may be eligible to earn commission and/or bonuses + benefits.
Responsibilities
Educate physicians on device handling, implantation and troubleshooting techniques related to Inari products.
Develop, lead and/or facilitate training sessions and in-service education programs in the hospital environment.
Identify therapy adoption opportunities in collaboration with Regional and Account Managers in local geographies.
Communicate highly technical information clearly and effectively during fast-paced procedures.
Act as a clinical interface between the medical community and the Company.
Requirements
Bachelor’s degree preferred or Associates Degree in nursing or clinical required
Support product innovation, claims, labelling and compliance across Danone and the MADE Group
Locations (2)
Sydney, New South Wales, Australia
Melbourne, Victoria, Australia
Responsibilities
Conduct first-line reviews of formulations, ingredients, labels, claims and communication materials against regulatory requirements and company guidance
Support compliance assessments and identify matters requiring escalation to senior Regulatory Affairs colleagues
Maintain accurate regulatory documentation, records and assessments
Support the development and maintenance of regulatory guidance documents and resources
Provide regulatory support for innovation and renovation projects
Requirements
Bachelor's degree in Food Science, Nutrition, Biomedical Science, dietetics or another relevant scientific discipline
Coordinate and track day‑to‑day regulatory activities for MedSurg / Apheresis products, ensuring compliance with local and international regulations.
Responsibilities
Coordinate, obtain, notarize, legalize, compile and distribute documentation required to support international regulatory submissions.
Organize, maintain and archive regulatory submission files and records within RIMSys.
Maintain and update product registration metadata in regional and national regulatory databases, including EUDAMED and applicable national databases.
Communicate and coordinate with internal stakeholders, distributors and other external partners regarding regulatory documentation and registration activities.
Contribute to the preparation and maintenance of EU Technical Files and ensure appropriate documentation is stored within the Agile document repository.
Requirements
Bachelor’s degree in Life Sciences, Regulatory Affairs, Quality, Business Administration, or a related field
Coordinate the collection, tracking, review, and maintenance of site regulatory and essential documents to support site activation and ongoing study requirements.
Compensation
The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):
United States of America - $60,000.00 - $119,000.00
Responsibilities
Coordinate the collection, tracking, review, and maintenance of site regulatory and essential documents to support site activation and ongoing study requirements.
Partner with study teams, sites, and functional stakeholders to ensure timely completion of start-up activities and activation milestones.
Review study-specific regulatory documentation, identify gaps or quality issues, and drive corrective actions prior to final approval.
Support the development, adaptation, and review of country- and site-specific informed consent documentation.
Facilitate site identification and feasibility activities, including confidentiality agreements, feasibility questionnaires, and site qualification efforts.
Requirements
Bachelor's degree in medical, biological, physical, health, pharmacy, or another related scientific discipline
Coordinate the collection, tracking, review, and maintenance of site regulatory and essential documents to support site activation and ongoing study requirements.
Compensation
The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):
United States of America - $60,000.00 - $119,000.00
Responsibilities
Coordinate the collection, tracking, review, and maintenance of site regulatory and essential documents to support site activation and ongoing study requirements.
Partner with study teams, sites, and functional stakeholders to ensure timely completion of start-up activities and activation milestones.
Review study-specific regulatory documentation, identify gaps or quality issues, and drive corrective actions prior to final approval.
Support the development, adaptation, and review of country- and site-specific informed consent documentation.
Facilitate site identification and feasibility activities, including confidentiality agreements, feasibility questionnaires, and site qualification efforts.
Requirements
Bachelor's degree in medical, biological, physical, health, pharmacy, or another related scientific discipline
Contributing to Magnetic Resonance Imaging (MRI) pulse sequence development, translating novel concepts into robust product solutions for clinical MR applications.
Compensation
The base salary range for this role is EUR 50,750.00 - EUR 79,750.00. This role is eligible for 3% short term incentive
Responsibilities
Developing, adapting and innovating MR pulse sequences to enable new clinical contrasts and improve image quality, clinical functionality and usability
Bringing clinical MR features from research stage through advanced development to the market
Translating clinical and technical needs into product requirements, prototyping and demonstrating feasibility
Creating software designs aligned with product requirements and software architecture
Engineering concepts into robust product solutions, including implementation, automated testing and verification
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