"Alerted.org

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.