About Us
Based in Barcelona and Treviso, INDIBA Group stands at the forefront of global leadership in Aesthetics, Beauty, Rehabilitation, Sports, Intimate Health, Pharma, and Animal Health solutions, with a rich 40-year history of scientific innovation.
Our cutting-edge 448 kHz frequency technology is the cornerstone of our therapies, empowering individuals to enhance their lives and recover from injuries across various sectors.
With the integration of K-LASER, a global leader in medical lasers, we are committed to advancing treatments, embracing new technologies, and expanding our global presence in medical research.
Our mission is revitalizing lives, and our teams work daily towards this goal.
What are we looking for?
We seek a senior leader to oversee the Medical Affairs & Training Department. This strategic role combines regulatory and clinical responsibilities with scientific communication and training leadership. The ideal candidate will have deep medical expertise, stakeholder engagement skills, and the ability to translate clinical insights into business value while supporting our company positioning.
Responsibilities
1. Lead the development and strategic use of clinical evidence to support product registration and ensure compliance with global medical device regulations.
2. Oversee the preparation of clinical documentation, including trial protocols, regulatory submissions, and reports to health authorities and notified bodies.
3. Supervise clinical trials and post-market surveillance, maintaining relationships with key opinion leaders and investigators.
4. Represent the medical department in audits, inspections, and quality reviews requiring scientific expertise.
5. Provide scientific support and strategic guidance to internal departments such as Commercial, Marketing, R&D, Regulatory, and Quality.
6. Guide the development of scientific materials, publications, and conference contributions to enhance our position in the medical community.
7. Lead the Training team to deliver high-quality programs aligned with clinical data, product claims, and corporate goals.
8. Monitor emerging clinical trends and innovations to inform product development and positioning.
9. Ensure the effectiveness of the medical vigilance system in collaboration with relevant departments.
Candidate Requirements
1. Minimum of 10 years’ experience in Pharmaceutical, Medical Devices, or regulatory consultancy sectors, in areas such as Medical/Scientific Department, Clinical Research, Medical Writing, or Scientific Marketing.
2. Experience in writing clinical reports (expert reports, review reports, clinical/pharmacological/pharmacovigilance studies, phase III/IV studies).
3. Degree in Health Sciences (Medicine, Pharmacy, Human Biology, or Biomedical Science); postgraduate studies in Pharmaceutical, Cosmetic, or Aesthetic/Rehabilitation Medicine are a plus.
4. Strong knowledge of clinical research methodology.
5. Fluent in Spanish and English, both verbal and written; additional languages are a plus.
What We Offer
* Full-time, permanent contract.
* Location: Sant Cugat del Vallés.
* Hybrid work model.
* Attractive remuneration package and fringe benefits.
* Multinational, flexible environment.
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