Source description
About the role
As an experienced and strategic Head of Scientific & Statistical Reporting at MS Clinical Research, your role involves leading the scientific reporting and data analytics function. You will oversee the end-to-end scientific report generation, interpret clinical/study data, manage statistical reporting, and lead the Data Analytics team. Your expertise in clinical data interpretation, scientific writing, statistical reporting methodologies, and team leadership will be essential for delivering high-quality reports to sponsors, investigators, and internal stakeholders. Key Responsibilities: - Lead the overall scientific and statistical reporting function across clinical studies and research projects. - Oversee preparation, review, and finalization of scientific reports, analytical summaries, and study outcome documents. - Develop standardized reporting templates, workflows, and quality benchmarks. - Interpret clinical and study data to derive meaningful scientific insights and conclusions. - Lead, mentor, and manage a team of Data Analysts and reporting professionals. - Review and interpret complex clinical/study datasets for reporting purposes. - Manage end-to-end execution of scientific reporting projects within defined timelines. - Establish quality control processes for scientific and statistical reporting. Qualifications Required: - 1012 years of experience in Scientific Reporting, Clinical Data Analytics, Biostatistics, Medical Writing, or related domains. - Strong experience in scientific/study report writing and clinical data interpretation. - Proven experience in leading and managing data/reporting teams. - Proficiency in Excel, SQL, and data analytics/reporting tools. - Excellent written and verbal communication skills. The company prefers candidates with experience in Clinical Research, CRO, Healthcare Analytics, or Scientific Reporting environments. Exposure to eCRF/study data handling, and understanding of regulatory and compliance requirements in clinical research are also valued. Your ability to think analytically, lead teams effectively, interpret statistics, and manage stakeholders will be crucial in this role. As an experienced and strategic Head of Scientific & Statistical Reporting at MS Clinical Research, your role involves leading the scientific reporting and data analytics function. You will oversee the end-to-end scientific report generation, interpret clinical/study data, manage statistical reporting, and lead the Data Analytics team. Your expertise in clinical data interpretation, scientific writing, statistical reporting methodologies, and team leadership will be essential for delivering high-quality reports to sponsors, investigators, and internal stakeholders. Key Responsibilities: - Lead the overall scientific and statistical reporting function across clinical studies and research projects. - Oversee preparation, review, and finalization of scientific reports, analytical summaries, and study outcome documents. - Develop standardized reporting templates, workflows, and quality benchmarks. - Interpret clinical and study data to derive meaningful scientific insights and conclusions. - Lead, mentor, and manage a team of Data Analysts and reporting professionals. - Review and interpret complex clinical/study datasets for reporting purposes. - Manage end-to-end execution of scientific reporting projects within defined timelines. - Establish quality control processes for scientific and statistical reporting. Qualifications Required: - 1012 years of experience in Scientific Reporting, Clinical Data Analytics, Biostatistics, Medical Writing, or related domains. - Strong experience in scientific/study report writing and clinical data interpretation. - Proven experience in leading and managing data/reporting teams. - Proficiency in Excel, SQL, and data analytics/reporting tools. - Excellent written and verbal communication skills. The company prefers candidates with experience in Clinical Research, CRO, Healthcare Analytics, or Scientific Reporting environments. Exposure to eCRF/study data handling, and understanding of regulatory and compliance requirements in clinical research are also valued. Your ability to think analytically, lead teams effectively, interpret statistics, and manage stakeholders will be crucial in this role.