Medical Research Director

Lead 1. Research Project Leadership

· Design, coordinate, and supervise internal research projects.

· Coordinate with external research centers on basic, preclinical, and applied research projects related to new active ingredients, formulations, etc.

· Assess scientific, clinical, and economic feasibility of R&D projects.

· Ensure technical and regulatory quality of studies conducted in collaboration with universities, hospitals, or research centers.

· Drive innovation and knowledge transfer into the product development pipeline.

· Evaluate external research or co development licensing projects.

· Lead the preparation, submission, and coordination of the Profarma Plan.

2. Clinical Research Management

· Design, coordinate, and supervise clinical trials.

· Ensure compliance with Good Clinical Practice (GCP), European and Spanish regulations, and AEMPS guidelines.

· Coordinate interactions with investigators, CROs, ethics committees, and dermatology centers.

· Review and approve clinical trial protocols, informed consents, reports, and scientific publications.

· Lead dissemination of clinical results and strengthen the company's scientific presence at national and international congresses.

3. Medical Affairs & Healthcare Engagement

· Lead the Medical Affairs function and align its activity with corporate strategic objectives.

· Build strong relationships with dermatologists, scientific societies, hospitals, and Key Opinion Leaders (KOLs).

· Provide medical and scientific support to Marketing, Commercial, and Communication teams, ensuring rigor and ethical standards.

· Oversee medical review of promotional materials, product technical sheets, and claims.

· Promote internal medical training on products, dermatological conditions, and clinical trends.

· Attend medical congresses and support scientific collaborations with the international division.