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Life science project manager (clinical trials healthcare projects for samd)

El Cerro
Legit.Health
Publicada el 3 mayo
Descripción

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.

Job Description

We are looking for a Life Science Project Manager focused on clinical trials and healthcare innovation with expertise in software medical devices, eager to drive innovation in digital health.

Responsibilities
* Lead development and implementation of transformative projects in healthcare technology from conception to delivery.
* Bridge the gap between commercial, clinical, and technical teams, translating customer needs into actionable specifications.
* Work with partners (hospitals, CROs, research institutions) to ensure proper study design, execution, and integration of our technology into customer workflows.
* Collaborate with the Deal Owner and Customer Success Manager, focusing on implementation, delivery, execution, and providing clinical, technical, and regulatory advisory to the customer.
* Translate clinical and business needs into clear project plans and specifications, ensuring successful execution across all phases.
* Provide clinical, technical, and regulatory guidance while not managing the full client lifecycle.
* Develop and track detailed project plans, manage changes to scope and schedule, ensuring on‑time and on‑budget execution.
* Collaborate with customers, investigators, CROs, and Sponsors to ensure project success.
* Act as liaison between commercial and product teams, translating needs into technical specs.
* Offer expertise in product documentation, data protection, and regulatory feasibility.
* Conduct functional and technical requirements analysis.
* Provide holistic view of healthcare processes.
* Contribute to product strategy.
Qualifications
* Strong knowledge of Good Clinical Practice (GCP) and clinical research regulations.
* Proven experience in project management, especially in software medical device development in the health or digital health sectors.
* Specific knowledge of AI technologies in health and experience in dermatology or related fields.
* Understanding of medical device regulation and software device regulatory frameworks.
* Basic knowledge of data protection laws (GDPR, HIPAA).
* Deep understanding of the health industry, B2B dynamics, and software medical device regulations.
* Exceptional communication skills, with the ability to explain complex concepts clearly.
* Effective leadership experience with multifunctional teams.
* 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 CDMS, EDC platforms, and clinical trial software (Medidata, REDCap, OpenClinica).
* Knowledge of healthcare processes and systems (HIS/EHR/EMR, RIS, LIS, PACS, ERP) and standards such as FHIR and HL7v2.
* Foundational programming knowledge in PHP, JavaScript, or Python.
Important
* Ability to work autonomously, with discipline and high motivation.
* Proactive, willing to learn, with impact and growth orientation.
* Team player capable of adapting to a fast‑paced environment.
Benefits
* Full‑remote position with flexible working hours.
* Comprehensive remote collaboration tools (Slack, Hangouts).
* Flexible compensation: daycare and restaurant vouchers.
* Flexible vacation: 23 working days + 2 additional days (birthday & December 7) + 2 days for company closure per labor agreement.
* Full‑time contract with starting date as soon as possible.
* Competitive salary based on experience.
* High proficiency in Spanish and English required; additional languages are a plus.
Other information

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.

Please note that this is not an email to submit job applications. We are only processing the data you have provided for specific personnel selection processes. If you wish to apply for a position, please follow the instructions on our official job postings.

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