Descripción de la oferta
About Us
Legit.Health deploys computer vision and artificial intelligence technology to enable lifesaving diagnosis and therapies for visible diseases. Our goal is to enable universal access to high‑quality diagnosis and follow‑up of pathologies and to offer affordable health assistance to everyone everywhere.
About the Role
We are looking for a passionate Life Science Project Manager focused on clinical trials, healthcare innovation, and software medical devices. You will lead transformative projects from conception to delivery, bridging commercial, clinical, and technical teams, translating customer needs into actionable specifications and ensuring solutions meet high standards, budget, time constraints, and regulatory requirements.
Key Responsibilities
Lead development and implementation of transformative projects in healthcare technology.
Translate customer needs into actionable specifications and ensure solutions meet high standards, budget, time constraints, and regulatory requirements.
Collaborate with partners (hospitals, CROs, research institutions) to design, execute, and integrate technology into workflows.
Work alongside the Deal Owner and Customer Success Manager to focus on implementation, delivery, and clinical/regulatory advisory.
Develop and track detailed project plans, manage scope changes, schedule, and ensure successful execution within constraints.
Daily customer interaction with investigators, CROs, and sponsors.
Act as liaison between commercial and product teams, facilitating communication.
Provide technical/regulatory advisory to customers regarding software medical device use cases, technical aspects, regulatory feasibility, and data protection.
Assess project needs and specifications for alignment with product objectives and customer expectations.
Offer a comprehensive perspective of healthcare processes to support solution development.
Define development requirements and produce accurate product documentation.
Participate in product strategy definition and adjustment.
Required Qualifications
Strong knowledge of Good Clinical Practice (GCP) and clinical research regulations.
Proven experience in project management, especially in software medical device development within health, biotech, or digital health sectors (hospitals, CROs, sponsors, research institutions).
Specific knowledge of AI technologies applied to health and experience in dermatology or related fields.
Understanding of medical device regulation and familiarity with software medical device regulatory frameworks and compliance.
Basic knowledge of data protection laws (GDPR, HIPAA).
Deep understanding of the health industry, B2B dynamics, and specific regulations for software medical devices.
Exceptional communication skills to interact effectively with technical teams, healthcare professionals, and business stakeholders.
Leadership experience leading multifunctional teams in dynamic environments.
Degree in Business Administration, Health Management, Biotechnology or related field. Project management certification (PMP, PRINCE2) highly valued.
Nice to Have
Experience with data transfer specifications, database structures, and system integrations in clinical or research studies.
Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) platforms, and clinical trial software (Medidata, REDCap, OpenClinica).
Knowledge of healthcare processes and management systems (HIS/EHR/EMR, RIS, LIS, PACS, ERP) and standards (FHIR, HL7v2).
Foundational programming knowledge (PHP, JavaScript, Python).
Important
Able to work autonomously, with discipline and high motivation and energy.
Proactive, willing to learn, and eager to grow.
Team player capable of adapting to changes in a fast‑paced environment.
Benefits and Working Conditions
Full‑remote position with flexible working hours.
Full‑time contract, starting ASAP.
Competitive salary based on experience.
Flexible vacation policy: 23 working days per year + 2 additional company days + 2 days for company closure.
Flexible compensation: daycare and restaurant options.
Language requirements: high proficiency in Spanish and English (written & spoken); additional languages a plus.
Working in a fast‑growing start‑up environment within an international context.
Data Processing Statement
In compliance with the provisions of the data protection regulations, we inform you that the personal data you have provided with your resume will be processed in a mixed manner (automated or not) by AI Labs Group, S.L., with NIF B****** and address in Gran Vía, 1, BAT Tower, Bilbao (Bizkaia), ***** (hereinafter, Legit.Health). The purpose of this data processing is the management of Legit.Health's personnel selection processes and is based on your prior consent. Your data will be kept for one year, after which we will proceed to cancel it. You are also informed that no automated decisions will be made. Your data will not be transferred to third parties. At any time you can exercise your rights of access, rectification, deletion, portability, limitation, or opposition, by writing to the email *****. We also inform you that you can go to the Control Authority to assert your data protection rights.
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