Job Description

**General Description:** We are seeking a highly skilled and dedicated Statistician with a specialized focus on Patient Reported Outcome (PRO) analyses to join our dynamic team. The ideal candidate will have a strong background in statistical methodologies and experience in handling patient-reported data to draw meaningful insights. Functioning as a mentor or manager in the stat group. Located in EU or US. **Essential Functions of the job:** This role is crucial in advancing our understanding of patient experiences and improving healthcare outcomes through rigorous analytical approaches. **Responsibilities:** + Data Management and Analysis: Conduct statistical analyses on patient-reported outcome data, ensuring accuracy, validity, and reliability of results. + Methodological Development: Develop and implement advanced statistical methods and models tailored to patient-reported outcome measures (PROMs). + Research and Reporting: Lead research projects involving PRO analyses, prepare comprehensive reports, and present findings to stakeholders. + Collaboration: Work closely with cross-functional teams, including clinical researchers, data scientists, and healthcare professionals, to integrate PRO data into broader research initiatives. + Data Interpretation: Translate complex statistical findings into actionable insights that can inform clinical practices and policy decisions. + Quality Assurance: Ensure the highest standards of data quality and integrity in all analyses and reports. + Training and Mentorship: Provide guidance and support to junior statisticians and other team members in the area of PRO analyses. **Computer Skills:** Microsoft office apps, SAS and R **Other Qualifications:** + PhD or equivalent degree in statistics/biostatistics or related discipline with a minimum of 5 years relevant work experience, or a Master's degree with a minimum of 7 years relevant work experience (see each box for detailed year requirement). + Experience in the healthcare or pharmaceutical industry. + Familiarity with regulatory guidelines related to patient-reported outcomes. + Published research in peer-reviewed journals on topics related to PRO analyses. + Experience in designing and validating patient-reported outcome measures. + Solid knowledge of statistical analysis methodologies and experimental design. + Solid working knowledge of statistical and data processing software e.g. SAS and/or R. + Strong good presentation, oral and written communication skills. + Ability to learn, being proactive, motivated, and consistently focus on details and execution. + Strong demonstrates interest in statistical research activities and application of novel methods to clinical trial development. + Ability to work in a team environment with clinical team members. + Knowledge of clinical trial design concepts; In-depth knowledge of all phases of the drug development process. + Demonstrated skill in the planning, analysis and reporting of clinical trials. **Travel:** Yes, depends on needs. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

Job Tags

Work experience placement, Work at office,

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