
11 - 50 employés
Fondée en 2002
🏥 Santé
💼 Conseil
📦 Logistique
Healthcare • Consulting • Logistics
Praxis est une entreprise dédiée à la connexion des patients avec des opportunités significatives d'essais cliniques. En mettant l'accent sur la création de programmes de recrutement sur mesure, Praxis utilise une variété d'outils spécialisés et une vaste expérience dans divers domaines thérapeutiques pour s'assurer qu'ils atteignent les bons patients dans le monde entier. Fondée en 2002, l'entreprise souligne l'importance de l'engagement des patients et utilise des analyses de données sophistiquées pour améliorer le parcours des patients dans la recherche clinique.
🕒 il y a 1 mois
🇺🇸 États-Unis – Télétravail
💵 $205 000 - $225 000 / an
⏰ Temps Plein
🟠 Senior
👔 Directeur
🦅 Parrain de Visa H1B
👻 Score fantôme 20%
🗣️🇺🇸🇬🇧 Anglais requis
D'où vient cette offre
Publiée sur la page carrières de Praxis, pas via un site d'emploi
Repérée par Remote Rocketship il y a 1 mois
Toujours ouverte sur le site de Praxis. Vérifiée il y a 8 heures.

11 - 50 employés
Fondée en 2002
🏥 Santé
💼 Conseil
📦 Logistique
Healthcare • Consulting • Logistics
Praxis est une entreprise dédiée à la connexion des patients avec des opportunités significatives d'essais cliniques. En mettant l'accent sur la création de programmes de recrutement sur mesure, Praxis utilise une variété d'outils spécialisés et une vaste expérience dans divers domaines thérapeutiques pour s'assurer qu'ils atteignent les bons patients dans le monde entier. Fondée en 2002, l'entreprise souligne l'importance de l'engagement des patients et utilise des analyses de données sophistiquées pour améliorer le parcours des patients dans la recherche clinique.
• Drive the drug-device combination program end to end from device design and verification through risk management and design history file ownership • Set strategy, build integrated timelines, manage risk, and maintain scope, quality, and deadlines • Shape the FDA regulatory strategy while coordinating device and drug considerations • Keep the program inspection ready and submission ready at every stage • Translate between pharmaceutical development and device engineering so both advance in lockstep • Align and mobilize scientific, regulatory, quality, clinical, and operations teams across disciplines and seniorities • Serve as the day-to-day interface with the technology partner • Direct and integrate external device and regulatory consultants • Perform hands-on technical problem solving across electronics, software, electrochemistry, and delivery hardware • Present progress, risks, and decisions to executive leadership
• Personally led the technical development of a drug-device combination product spanning device design and engineering, verification and validation, human factors, and combination product risk management • Experience taking specific combination products or delivery systems from early development through design transfer, submission, or launch • Demonstrable FDA device regulatory experience, including 21 CFR Part 4, design controls, and premarket submissions • Background or experience in electrical engineering projects or a closely related field, with genuine technical depth • Working understanding of pharmaceuticals and devices and how they come together • Knowledge of combination product quality systems (ISO 13485), risk management (ISO 14971), human factors/usability engineering (IEC 62366), on-body/wearable delivery system requirements (ISO 11608, including Part 6), and medical electrical equipment safety (IEC 60601) • Evidence of leading people and programs while also delivering technical work personally • Ability to coordinate diverse specialists and work with external partners and consultants • Comfort and credibility presenting to and being challenged by senior leadership • Highly desirable technical breadth in electronics and embedded hardware design, software/firmware development, electrochemistry, implantable or body-worn device development, wearable/transdermal delivery device development, or combination product DHF/technical file/design control documentation ownership • Comfort operating iteratively, adapting quickly, and making progress amid ambiguity • Ability to build trust across organizations, take ownership, follow through, give and receive direct feedback, and work with urgency while maintaining quality and compliance
• 99% of the premium paid for medical, dental and vision plans • Company-paid life insurance • Company-paid AD&D • Disability benefits • Voluntary plans to personalize coverage • Dollar-for-dollar 401(k) matching up to 6% on eligible contributions • Long-term stock incentives • ESPP • Discretionary quarterly bonus • Extremely flexible wellness benefit • Generous PTO • Paid holidays • Company-wide shutdowns
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