Scientific Project Manager
il y a 4 semaines
icometrix is a fast-growing company focused on impacting the lives of people with neurological conditions through its unique AI solutions that assist radiologists and neurologists in the reading of brain MRI and CT scans. The headquarters are based in Leuven, Belgium, but icometrix already has a US team present.
Our customers include hospitals and pharmaceutical companies. The icobrain solutions for people with multiple sclerosis, Alzheimer's disease & other forms of dementia, stroke, brain trauma, and epilepsy, are already impacting clinical care decisions in many hospitals worldwide. Recently, based on the submitted evidence by icometrix, a new CPT III reimbursement code was issued by the AMA in the US, which is driving adoption of icobrain as the standard of care significantly.
The icometrix team includes enthusiastic, team-oriented and multi-cultural colleagues with a range of technical and medical backgrounds. We enjoy an innovative and challenging working environment and are driven by our core values: impact, trust, collaboration, respect, and crazitivity.
Icometrix acts throughout the healthcare system from providers, payers and pharmaceutical industry, as our AI solutions support improved personalised medicine of neurological disorders. As such, icometrix' studies team entails both icometrix' specific evidence studies as well as services for strategic pharmaceutical partnerships and trials. As scientific project manager, you will manage such studies, engage with key stakeholders and focus on generating impactful scientific evidence.
What will you do?- Coordinate clinical studies and trials towards generating optimal clinical and health economic evidence of the icometrix portfolio.
- Boost our neuro-imaging services to support optimal engagement of radiologists, neurologists, or other physicians aligned with the evidence strategy of icometrix.
- Take a pro-active lead in the evidence dissemination plan (including scientific writing).
- Manage milestones, deliverables, timelines, budget, and quality to allow optimal implementation of our imaging services and ePRO services.
- Monitor progress, report and present study status, timelines, budget and quality of your deliverables to the Project Team, Management and Customer.
- Lead study-specific decision-making, develop improvements for increasing study efficiencies and co-ordinate issue detection and resolution.
- Coordination of external partners (sites, additional vendors, both sponsor related as icometrix related).
- GCP compliant delivery and assure optimal coordination and communication for optimal implementations.
- Prepare and support potential audits and inspections.
- Have a critical view on the study results and Reporting proactively to the Team Manager on critical study-related issues.
- Monitor closely project related elements linked to data management, Risk assessment and execution, contribution for submission ethics committees.
- Participate in the development and coaching of less experienced staff.
- Master's degree or equivalent through working experience (preference for neuroimaging and/or engineering).
- Good stakeholder management and communication skills.
- Strong background in imaging and neurology is a plus.
- Experience in Clinical Trials is wishful.
- Clinical research or project management experience.
- Fit with our values and culture.
- Entrepreneurial and customer-oriented personality.
- Eager to learn with positive energy and a results-oriented attitude.
- Use problem-solving skills and appropriate resources to deal with requests and problems.
- Work accurately and independently as well as within a multidisciplinary team.
- A market conform wage.
- A job advancing healthcare and technology.
- A job in an innovative, growing company with a worldwide impact.
- A chance to work with experts in different areas and exchange ideas.
- An opportunity to have a direct impact on our product.
- An innovating and challenging environment.
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