Galderma Laboratories, LP
Medical Science Liaison (Biotech)
Strategic brands in the U.S. include Epiduo® Gel, Epiduo® Forte Gel, Oracea® Capsules, Clobex® Spray, Mirvaso® Gel, MetroGel® Gel, Soolantra® Cream, Vectical® Cream, Tri-Luma® Cream, Cetaphil®, Differin® Gel OTC, Restylane®, Restylane® Silk, Restylane ® Lyft, Restylane® Refyne, Restylane® Defyne, Dysport® and Sculptra® Aesthetic.
For more information, please visit www.galdermausa.com and www.galderma.com.
Galderma is an equal opportunity employer. M/F/D/V.
Develops on-going professional relationships with healthcare practitioners, clinical investigators, and healthcare decision makers to provide medical and scientific support for prioritized disease franchises within Prescription Business Unit. Facilitates Scientific Exchange with External Experts and Professional Societies within the healthcare community regarding new and emerging therapies. Gathers insights from healthcare practitioners on emerging unmet medical needs to facilitate input into the clinical development planning process. When appropriate, identify appropriate clinical investigators and facilitate placement into Galderma sponsored clinical trials.
• Integrate effectively within the Medical Affairs team providing product knowledge and expertise within each supported disease state.
• Prepare and Execute Key External Expert Engagement Plan.
• Develop 1:1 relationships with top scientific influencers and Professional Organizations.
• Produces, coordinates, and manages medical and scientific content for given medical area (e.g., abstracts, posters, publications, medical decks, speaker programs, advisory boards, educational programs, etc.).
• Serves as scientific expert in Galderma products and related medical areas for example at Medical Advisory Boards, Speaker Trainings and Internal Meetings, Field colleague training.
• Attend congresses, prepare summary, and present key perspectives to medical and respective medical/managed care teams.
• Actively contribute scientific insights and recommendations to business colleagues (i.e., colleagues inside and outside US Medical Affairs team) to help achieve company objectives.
• As Subject Matter Experts, provide additional internal review of scientific and promotional material when needed ensuring the integrity of the scientific data used.
• Provide SIG medical colleagues with US-based medical insights for global medical strategy development.
• Represents Galderma at medical meetings, conferences, advisory boards, etc.
Travel & Residency
Fort Worth, TX
• Medical doctor MD, PhD or PharmD.
• Minimum 1-3 years of related medical, regulatory affairs and/or research and development experience in the pharmaceutical, biotechnology, medical device and/or CRO (contract research organization) industry.
• Must have previous academic/research experience.
• Must demonstrate the ability to interface effectively with a variety of technical platforms for the collection, review, and dissemination of medical information.
• Must be proficient with MS Office.
• Ability to travel overnight as needed.
• Must demonstrate excellent interpersonal and communication skills (written and verbal) with strong personal integrity, teamwork abilities, and customer focus.
• Must have a successful track record demonstrating the ability to organize, prioritize and work effectively in a high-pressure, constantly changing environment.
• Solid understanding of FDA, OIG, HIPAA, and other regulatory guidelines relevant to the pharmaceutical industry; related experience within the United States (i.e. understanding of US regulatory environment).
• Knowledge of GCP practices and procedures.
• Expertise in relevant medical area is preferred.
• Demonstrated record of effective high quality scientific/medical publication is preferred.
• Must possess excellent written and verbal communication skills.
• Must possess meeting planning and facilitation skills.