Medical Expert, Clinical Sciences

Overview

Galderma is an emerging pure‑play dermatology leader with a science‑based portfolio of premium flagship brands and services that span the full spectrum of the dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology.

Job Title
:
Medical Expert, Clinical Sciences

Location
:
Boston, MA;
Miami, FL; or remote on the East Coast.

The Medical Expert, Clinical Sciences provides scientific and medical input to clinical development programs, collaborating with cross‑functional teams to ensure clinical activities align with regulatory standards, Good Clinical Practice, and company objectives. The role supports the development and writing of clinical documentation, medical insight during study conduct, and data interpretation.

• Works as part of a diverse, cross‑functional team responsible for the design, implementation, execution, and documentation of clinical studies supporting regulatory and business objectives.
• Provides scientific and clinical input (e.g., rationale, objectives, endpoints) to clinical development plans, Target Product Profiles, study outlines, protocols, investigator brochures, and other clinical documentation.
• Contributes as a therapeutic‑area scientific and medical expert in discussions with internal stakeholders (e.g., Clinical Development, Global Medical Affairs, Regulatory, and Product Strategy).
• Supports communication with external stakeholders (e.g., clinical investigators, CROs, and key opinion leaders) under guidance from senior colleagues or project leads.
• Provides medical support and safety medical monitoring during study conduct, addressing medically relevant questions and ensuring clinical data quality and integrity.
• Contributes to preparation of presentation materials for investigator meetings, protocol training sessions, and scientific advisory boards.
• Participates in the review and interpretation of clinical data in collaboration with study and development teams.
• Supports preparation of study reports, clinical summaries, and regulatory submissions as needed.
• Collaborates with Global Clinical Safety in evaluating the drug or device benefit‑risk profile, risk management activities and assists in documentation of safety‑related findings.
• Performs other duties as assigned.

• MD (or equivalent) required.
• At least 2–3 years of industry experience required.
• Experience in aesthetic dermatology or medical aesthetics preferred; injectable aesthetics experience advantageous.
• Strong knowledge of international guidelines ICH/GCP, and basic knowledge of GMP/GDP.
• Familiarity with global regulatory standards for medical devices and/or drugs.
• Strong understanding of the clinical development process, data management, and risk management principles.
• Fluent in English (written and oral).

The base salary range is $170,000–265,000, depending on experience, skill set and location. In addition to base salary, employees may participate in an annual short‑term incentive program based on corporate performance. The benefits program includes health insurance, a 401(k) plan with employer match, paid time off, hybrid work schedules and more.

• If your profile is a match, we will invite you for a first virtual conversation with the recruiter.
• The next step is a virtual conversation with the hiring manager.
• The final step is a panel conversation with the extended team.

This job description does not list all the duties of the job. You may be asked by your supervisors or managers to perform other duties. You will be evaluated in part based on your performance of the tasks listed in this job description. The employer has the right to revise this job description at any time. This job description is not an employment contract, and either you or the employer may terminate employment at any time, for any reason.

In addition, reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.