Sr Clinical Scientist

Job description

Whether it's the unique breadth of our integrated offering that covers Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology products; or our commitment to recognizing and rewarding people for the contribution they make - working here isn't like anywhere else. At Galderma, we actively give our teams reasons to believe in our 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. At Galderma we’re unique and we embrace difference. Whether it’s the unique breadth of our integrated offering that covers Aesthetics, Consumer, and Prescription products; or our commitment to recognising and rewarding people for the contribution they make – working here isn’t like anywhere else. At Galderma, we actively give our teams reasons to believe in our 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. Key Responsibilities Clinical Development, Study Design & Conduct Provide scientific input to ensure clinical development activities are aligned with regulatory guidance, scientific rationale, and the evolving competitive landscape. Conduct and/or oversee targeted literature searches to support clinical development strategy, study design decisions, endpoint selection, and interpretation of emerging data. Lead the development of clinical study designs (Phase I–III, as applicable), in alignment with the overall development strategy. Manage the development of study protocols, protocol amendments, and clinical study reports (CSRs), ensuring scientific accuracy and consistency. Ensure that study endpoints, eligibility criteria, and assessments are clinically meaningful and scientifically appropriate, in collaboration with relevant subject matter experts. Provide scientific direction and oversight to contractor Medical Writers involved in the development of clinical and regulatory documents. Lead the development of the Master ICF and review country‑ and site‑specific ICFs to ensure alignment with the master and local regulatory and ethics requirements. Perform QC to ensure document consistency, accuracy, and formatting. Act as a key point of contact during study execution, providing protocol‑related guidance and clarification to Clinical Operations and study teams. Ensure appropriate filing of authored clinical documents in the TMF in accordance with company procedures. Work closely with Medical Experts, Biostatisticians, Clinical Operations, Safety, Regulatory Affairs, and other stakeholders to ensure integrated study delivery. Data Interpretation & Scientific Contribution Review and interpret clinical data and analyses in collaboration with the Study Team. Support the preparation of internal data review materials, e.g. IDMC charters and presentations. Regulatory & Clinical Documentation Contribute to, and where appropriate author, clinical sections of regulatory documents, including IND/CTA submissions, Investigator’s Brochures (IBs), CSRs, briefing documents, and responses to health authority questions. Manage the annual update of the Investigator’s Brochure (IB) in collaboration with cross‑functional stakeholders. SOP & Template Development Contribute to the development and maintenance of departmental SOPs, clinical document templates (e.g., protocol, IB, CSR), and writing guidelines, ensuring alignment with operational needs and regulatory requirements. Skills & Qualifications Education Bachelor’s degree in Life Sciences, Engineering, or a related field required; advanced degree (Master’s, PhD, or MD) preferred. Clinical or biomedical background relevant to drug development preferred. Experience Typically, 5–10 years of experience in clinical research or clinical development within the pharmaceutical, biotech, or CRO environment. Hands‑on experience contributing to clinical study design, conduct, and documentation (e.g., protocols, ICFs, IBs, CSRs). Experience working in cross‑functional study teams, in close collaboration with Medical Experts and Biostatisticians. Practical understanding of clinical data review and interpretation during study conduct. Experience overseeing or collaborating with Medical Writers and external vendors preferred. Technical & Regulatory Skills Strong knowledge of ICH‑GCP and clinical development regulations. Solid understanding of the clinical development lifecycle and regulatory documentation requirements. Experience with TMF requirements and document lifecycle management. Familiarity with governance activities such as IDMC participation and interim data review is an advantage. Core Competencies Strong scientific judgment and ability to critically evaluate clinical data and study designs. Excellent written and verbal communication skills, with the ability to convey complex scientific concepts clearly. High attention to detail, quality, and consistency in clinical documentation. Ability to manage multiple deliverables in a matrixed, cross‑functional environment. Proactive, collaborative, and solution‑oriented mindset. Next Steps If your application is successful and 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 Our people make a difference At Galderma, you’ll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do. Please add the content of the job posting here. It will be used to attract the best candidates so make sure to include the mission, responsibilities and requirements of the role.