Galderma
Sr Clinical Scientist Dermatology
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Clinical Development Lead – Clinical Development, Study Design & Conduct
About Galderma
Galderma is the emerging pure-play dermatology leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services spanning:
- Injectable Aesthetics
- Dermatological Skincare
- Therapeutic Dermatology
For nearly 40 years, we have focused our passion and expertise on the skin—the body’s largest organ—to meet individual needs through superior outcomes in partnership with healthcare professionals. Driven by our belief that the skin we are in shapes lives, we commit to advancing dermatology for every person’s unique story.
At Galderma, we seek driven, collaborative professionals who:
- Focus on delivering results
- Embrace continuous learning
- Energise their teams
- Bring initiative and teamwork
- Are passionate about impacting lives—consumers, patients, and clinicians.
We empower growth—individual and professional—while ensuring business needs are met now—and for the future. Our culture respects diversity, dignity, and individuality while fostering an environment where bold ambitions drive every team.
The Opportunity
At Galderma, work anywhere else feels different. Our unique blend of integrated dermatology offerings (Aesthetics, Consumer, Prescription) distinguishes us. We recognise and reward meaningful contributions. Join us to shape the future of dermatology, gain game-changing experiences, and leave a direct impact.
About the Role
We are seeking a passionate and experienced individual to join our Clinical Development team—focused on study design, execution, and scientific excellence—driving innovation from preclinical research through registration.
Key Responsibilities
🔬 Clinical Development, Study Design & Conduct
- Serve as a scientific quarterback, ensuring that clinical development aligns with regulatory guidance, competitive insights, and evolving drug development strategies.
- Conduct and oversee targeted literature reviews to:
- Inform clinical strategies, study design decisions, and emerging data interpretation
- Lead the development of clinical study designs (Phase I–III), aligning with Galderma’s development plans.
- Ensure protocol and study report accuracy, collaborating with subject matter experts to validate:
- Clinically meaningful study endpoints
- Appropriate eligibility criteria and evaluations
- Regulatory and ethical compliance
- Direct and manage 문의 함께 of cross-functional teams:
- Protocol development and amendments
- Protocol dev structures, CSRs
- Verify document consistency and quality (formatting, terminology) across global collaborations.
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📝 Regulatory & Documentation Trustee
- Partner in authoring and reviewing clinical sections of submissions, e.g.:
- Investigator’s Basebook (IB)
- responses To Health Authority
- Spearhead the annual update of IB and equivalent documents, with cross-team collaboration.
- Present clinical content with regulatory mark excellence to ensure successful filings.
💭 Data Interpretation & Strategic Content NS
- Collaborate with Study Teams, IDMC members, and external experts to:
- Review and interpret complex data effectively.
- Define crucial review tools (e.g., IDMC charters, summary analysis presentations).
- Drive sound scientific discussions during data review to optimise decision-making.
📋 SOP & Standard Streamlining
- Shape and maintain department SOPs and document templates (e.g., protocols, IBs, CSRs, writing guidelines) balancing business needs and regulatory compliance.
Mandatory Skills & Qualifications
Education
- Undergraduate degree in a Life Sciences or Pharmacy-related field required.
- Advanced degree (MSc, PhD, MD, etc.) highly recommended.
- Clinical or health sciences background required for regulatory and study led roles.
Experience
- 5–10 years in clinical research or drug development, within:
- Pharma/Biotech (priorities)
- Contract Research Organizations (CROs)
Hands-on experience with:
- Industry-standard practices, including all relevant phases (I-III):
- Protocols, ICFs (informed consent forms), IBs, eTMFs (electronic files), topic management.
- Management of multi-site, multi-countryrops.
- Collaboration with Medical Writers.
- Understanding interim data outcomes and regulatory teams.
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Core Competenies
- Sharp scientific judgment to critically evaluate:
- Study designs
- Correction data and summaries
- Inspiring written/verbal communication skill—perfect translating complex scientific concepts.
- Precision, quality awareness, impeccable documentation (to comply with slots and life spans).
- Multitasking ability in cross-functional and matrix environments.
- Collaborative mindset—innovative problem-solver with strong rigor; comfortable mediating situations.
Key Personal Traits
- ture high-caliber document reviewing
- Proactive ownership of tasks and relationships with stakeholders.
- We proactively seek different challenger members with ideas—but also positive energy in diverse cultures.
Reviewed and Preferred Qualifications
Technical Insights & Workflows
We value familiarity with/relevant experience in:
- ICH-GCP regulations and related global data standards。
- Accountable document handling precedents as per TMF system training documentation.
- Understanding and/or participation in Governance activities:
- IDMC (Independent Data Monitoring Committees) meetings, interim analyses.
Career Progress & Next Steps at Galderma
If your professional profile matches our requirements, we invite you into a structured period of engagement:
- Virtual introduction to the team (Recruiter)
- H8-diverse panel alignment with the Senior (lead))/Hiring Manager)
- Final interview with extended team along with qualification clarity
Meet Our People
Galderma Cultivates professional excellence through
- Philosophy of Purpose
- Professional respect
- Teamwork, collaboration & friendly support
We celebrate distance—and difference—to inspire inspired achievements.
For more details on developments: Galderma Careers.
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