Sr. Clinical Scientist

Monday to Friday 8 am to 4 pm ESTServes as a key role within the *** Aesthetics Research and Development team, the (Senior ) Clinical Scientist is responsible for contributing scientific and strategic expertise to our global clinical programs. Liaising with cross-functional study teams, this position requires a highly motivated, scientifically driven leader to contribute to the development of clinical strategy study design and execution, and data analysis and interpretation, delivering clear, consistent, and comprehensive results toward the registration of new aesthetic products and/or Client aesthetic indications.This position is initially offered as a six month fixed term contract with the potential to be considered for permanent employment thereafter, subject to business needs and individual performance.Should the candidate express interest in a permanent position, a relocation to Raleigh, NC would be required and is expected to be completed within three months of the start date, subject to mutual agreement and applicable policies Job Title/Position Direct Reports to Role Job Code (Senior) Clinical Scientist Reports To Function Division Matthias Hofmann Clinical Director Global Ax Career Band Job Grade Cost Center Location Employment Status CU1G25013 Raleigh, NC Contractor/ Temp Job Summary Serves as a key role within the Client's Aesthetics Research and Development team, the (Senior ) Clinical Scientist is responsible for contributing scientific and strategic expertise to our global clinical programs. Liaising with cross-functional study teams, this position requires a highly motivated, scientifically driven leader to contribute to the development of clinical strategy study design and execution, and data analysis and interpretation, delivering clear, consistent, and comprehensive results toward the registration of new aesthetic products and/or Client aesthetic indications.This position is initially offered as a six-month fixed-term contract with the potential to be considered for permanent employment thereafter, subject to business needs and individual performance.Should the candidate express interest in a permanent position, a relocation to Raleigh, NC would be required and is expected to be completed within three months of the start date, subject to mutual agreement and applicable policies. Responsibilities No. Major Duties Description 1 ccountable for contributing scientific expertise to the trial design phase of clinical projects under developmentProvide scientific and strategic input across various stages of clinical development to achieve market approval for new products and/or Client indications.a. Duties performed as a member of a cross-functional team of internal and external experts and in support of the clinical director.b. Projects are focused on medical devices, drugs, biologics, and/or other products for human use.c. Projects may span from in-development to post-marketing studies and products.Coordinate and integrate data and information from a variety of sources (e.g., internal and external studies, research documentation, and published literature) to support various clinical development initiatives.Consolidate input from internal and external contributors to develop appropriate key messaging.Support early-phase development activities, including curation, review, and interpretation of preclinical, exploratory data.Provide scientific guidance and technical expertise within teams, across departments, and across functions by providing strategic, actionable direction, creating a strong sense of team unity and identity, and providing positive, constructive feedback.Identify and troubleshoot study-specific issues, competing priorities, and clinical or scientific challenges.Ensure effective, accurate, and timely communication of key issues and progress to the team and senior management.Support planning and preparation for internal and external stakeholder meetings (e.g., workshops/summits, investigator meetings, scientific advisory boards, and regulatory meetings) 2 ccountable for authorship of various clinical documents, including clinical study outlines, clinical investigation plans and amendments, clinical investigation reports and investigators brochures, if applicable. Write, review, edit, and approve high-quality and timely clinical documents, contributing scientific/technical expertise related to clinical development and document preparation.Demonstrate understanding and interpretation of data generated from a variety of sources, including clinical study data and study results (i.e., tables, figures, and listings) and peer-reviewed literature and provide meaningful scientific interpretation and feedback to team members and other stakeholders.Communicate with and work effectively and productively with multidisciplinary, international teams while executing project plans.Ensure documents comply with current local and international regulations, laws, scientific and regulatory guidance, Good Clinical Practice, and internal policies and procedures.Proactively identify risks and escalate current/active/future issues; propose and enact solutions, developing contingency plans as needed.Ensure the successful execution and presentation of critical documents to leadership. 3 ccountable for contributing scientific expertise to the trial set-up and execution phases of clinical projects, including results interpretation and reporting Support, as a member of a cross-functional team the selection of relevant COAsSupport and provide scientific input for activities related to the development/validation of project specific COAs 4 ccountable for contributing scientific expertise to regulatory activities Provide scientific input for clinical parts of key regulatory and project documents (e.g., Clinical Evaluation Plan (CEP) and Report (CER), Instructions for Use, and Post-Market Clinical Follow-up Plan (PMCFP) and Report (PMCFR).Provide scientific input for appropriate disclosure of clinical trial data in public registries. 5 ccountable for contributing scientific expertise to the presentation and publication of clinical trial results Prepare and present trial data, to internal and external stakeholders, using clear, concise, and consistent result summaries.Provide scientific and written expertise for manuscripts, abstracts, and poster submissions in collaboration with R&D, Medical Affairs, and Commercial colleagues.Demonstrate knowledge of Good Publication Practices and editorial policies and apply expertise to publishing projects 6 ccountable for providing oversight of external medical writing vendors Effectively manage assigned writing projects, including projects outsourced to vendors.Oversee and review work of external writers to ensure Client's SOPs are followed, correct templates are used, and quality is maintained. Essential Skills Lead Self Lead Others Time Management Digital AcumenProblem SolvingEmotional IntelligenceResiliencyCommunication LeadershipCollaborationProject ManagementMotivate & Influence Technical & Functional SkillsDemonstration of excellent verbal and written English, including understanding of English language usage in clinical/technical environments and standardized-writing styles.Understanding of clinical product development, clinical trials, and global regulatory submissionsKnowledge of FDA and/or EMA regulations, GCP, ICH guidelines, and/or ISO 14155Able to work on multiple projects simultaneously, while maintaining competing priorities, timelines, and quality of deliverablesReadily adaptable to changes in priorities Minimum Qualifications MSc in Life Sciences Preferred Qualifications PhDDr PHMD Travel Requirements Up to 5 % Physical Requirements This position requires you to sit, stand and perform general office functions. You may also be required to lift up to twenty-five pounds occasionally. Bending, stooping and reaching are also frequently required. Equal Employment Opportunity It is our policy to provide equal employment opportunity for all applicants and colleagues. This policy includes our commitment to ensure that all employment decisions are made without regard to race, color, religion, gender, national origin, disability, pregnancy, veteran status (including Vietnam era veterans), age, sexual orientation, gender identity, or any other non-job-related characteristic protected by law.