Medical Affairs & Training Director
hace 13 días
Sant Cugat del Vallès
Join to apply for the Medical Affairs & Training Director role at INDIBA Group Join to apply for the Medical Affairs & Training Director role at INDIBA Group Get AI-powered advice on this job and more exclusive features. 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, standing on a rich 40-year history of scientific innovation. 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, standing on a rich 40-year history of scientific innovation. Our cutting-edge 448 kHz frequency technology is the cornerstone of our world-renowned therapies, empowering individuals to enhance their lives and accelerate recovery from injuries across various sectors. With the integration of K-LASER, a global leader in medical lasers, we’ve propelled our commitment to advancing treatments, embracing new technologies, and expanding our global presence in medical research. Revitalizing lives is what we do and what our teams are working on to achieve daily. What are we looking for? We are looking for a senior leader to oversee the Medical Affairs & Training Department for INDIBA Group. This strategic role combines regulatory and clinical responsibilities with scientific communication and training leadership. The ideal candidate will bring deep medical expertise, strong stakeholder engagement capabilities, and the ability to align and transform clinical insights into business value while supporting company positioning. Which will be your responsabilities? • Lead the development, maintenance, and strategic use of clinical evidence to support product registration and ensure compliance with global medical device regulations., • Oversee the preparation of clinical documentation, including trial protocols, regulatory submissions, and reports to health authorities and notified bodies., • Supervise clinical trials and post-market surveillance, maintaining strong relationships with key opinion leaders (KOLs) and investigators to support research and product positioning., • Act as a key medical representative in audits, inspections, and quality reviews requiring scientific justification or expertise., • Provide scientific support and strategic guidance across internal departments including Commercial, Marketing, R&D, Regulatory and Quality., • Guide the development of scientific materials, publications, and congress contributions to reinforce K-LASER and INDIBA's position in the medical community., • Lead the Training team to ensure delivery of consistent, high-quality programs aligned with the latest clinical data, approved product claims, and corporate objectives., • Monitor emerging clinical trends and innovations to inform product development and positioning., • Minimum of 10 years’ experience in Pharmaceutical Laboratory, Medical Devices company or regulatory consultancy, in areas such as Medical / Scientific Department, Clinical Research, Medical Writing, Scientific marketing or equivalent., • Experience in writing clinical reports (expert reports, review reports, clinical, pharmacological, pharmacovigilance, phase III / IV studies, or similar) is essential., • Academic background : Degree in Health Sciences (Medicine, Pharmacy, Human Biology or Biomedical Science). Master's or post-graduate studies aimed at the Pharmaceutical, Cosmetic and / or Aesthetic and Rehabilitation Medicine Industry as well cinical trial monitoring will be valued., • Good command of Clinical research methodology., • Full-time and permanent contract., • Attractive remuneration package. Seniority level Not Applicable Employment type Employment type Full-time Job function Job function Health Care Provider Medical Equipment Manufacturing Referrals increase your chances of interviewing at INDIBA Group by 2x Executive Director, Oncology Cell & Gene Therapies Global Medical Director Therapeutic Dermatology Medical Director, Senior Patient Safety Physician Oncology Associate Director, Medical Governance & Risk Management Global Medical director Immunology and Inflammation – Nemolizumab Senior Clinical Development Medical Director - Renal Senior Clinical Development Medical Director - Renal Associate Medical / Medical Director - Nephrology, EMEA Clinical Development Medical Director - Rheumatology Associate) Medical Director - Neurology Senior) Medical Director - Rheumatology (Client - dedicated), EMEA Manager, Medical Affairs - Iberia (Spain & Portugal) Associate Director, Safety Scientist, Global Patient Safety Associate Director, Safety Scientist, Global Patient Safety Associate Director, Safety Scientist, Global Patient Safety Project Manager / Sr Project Mgr - FSP - EMEA - Global Medical Affairs Sales Manager Europe - Active Medical Devices Director, Statistical Science - Global Medical Affairs / Payer Biometrics We’re unlocking community knowledge in a new way. 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