Galderma is the emerging pure-play dermatology category leader present in approximately 90 countries. We deliver an innovative science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981 we have dedicated our focus and passion to the human bodys largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin we are in shapes our lives we are advancing dermatology for every skin story.

We look for people who focus on getting results embrace learning and bring a positive energy. They must combine initiative with a sense of teamwork and collaboration. Above all they must be passionate about doing something meaningful for consumers patients and the healthcare professionals we serve every day. We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company we embrace diversity and respect the dignity privacy and personal rights of every employee.

At Galderma we actively give our teams reasons to believe in our bold ambition to become the leading dermatology company in the world. With us you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled direct impact.

The Senior Medical Expert Clinical Sciences is responsible for providing scientific input leadership and expertise to clinical programs including leadership and strategy to the Clinical Development Plan and execution of clinical protocol(s).

ESSENTION FUNCTIONS:

• Works as part of a diverse cross-functional team accountable for the design implementation execution and submission/approval of a Clinical Development Plan to support decision milestones regulatory requirements and budget targets.

• Provides clinical/medical strategy and input (i.e. scientific rationale objectives end points) to clinical development plans Target Product Profiles study outlines and protocols investigator brochures investigator meetings briefing packages CTDs draft labels and other documentation as required.

• Serves as therapeutic area scientific and clinical/medical expert with external stakeholders (e.g. regulatory authorities trial investigators & site staff CRO key opinion leaders advisory boards patient advocacy groups) and internal stakeholders (e.g. Research and Development Global Medical Affairs Global Product Strategy)

• Advises investigators and/or CROs on medically relevant questions emerging during study execution

• Develops presentation materials for trial-related advisory boards investigator meetings and protocol training meetings.

• Supports ongoing review of clinical trial safety data medical monitoring activities final analysis and interpretation in collaboration with development team members

• Supports development team on medical/scientific aspects of data review SSRM coding edit checks CRF DMC and other study documents.

• Evaluates continuously the drug/medical device benefit risk profile including the aspects of relevance to patients in clinical studies as well as external stakeholders (e.g. health authorities) in collaboration with Global Clinical Safety team

• Supports publications and clinical communication strategy in conjunction with Global Medical Affairs

• Serve as member of the inspection readiness team in preparation of a regulatory inspections.

• Other duties as assigned

EDUCATION KNOWLEDGE & SKILLS:

• MD required

• At least 3-5 years of industry experience required

• Dermatology or medical aesthetics clinical development experience required injectable aesthetics experience preferred

• Excellent knowledge of international guidelines ICH/GCP basic knowledge of GMP/GDP

• Excellent knowledge of relevant global regulations

• Excellent understanding of the drug and medical device development and risk management processes

• Excellent understanding of Clinical Trial Management including monitoring study drug handling and data management

• Fluent in English (written and oral)

Employers Rights:

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 upon 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 a contract for employment 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.