Overview Certara accelerates medicines using proprietary biosimulation software, technology, and services to transform traditional drug discovery and development. Its clients include more than 2,000 biopharmaceutical companies, academic institutions and regulatory agencies across 62 countries. The Associate Director, Data Sciences, leads the development, quality assurance, and delivery of clinical trial outcome databases across therapeutic areas. This role combines strategic planning, technical expertise , project management, and stakeholder engagement to support evidence synthesis, meta-analysis, and data-driven insights. Responsibilities Database & Quality Assurance : Oversee database development, curation, QC, and deployment to platform (e.g., CODEX); ensure accurate data extraction from literature and plots; validate QC documentation and manage change impact. Technical Expertise : Conduct systematic literature reviews using PICOS, ontologies, and data standards; refine search strategies; apply clinical trial knowledge; perform R-based quality checks and exploratory analyses. Project Management : Lead planning and delivery of database products; manage resources, timelines, and change controls; ensure clear communication with clients and internal teams. Team Leadership : Mentor teams ; drive process improvement, agile practices, and learning initiatives; support hiring and onboarding. Stakeholder Collaboration : Align with clients and internal teams on expectations; review project metrics and identify enhancements. Continuous Learning : Stay current with advancements in statistics, R, SLR, and data science; contribute to innovation. Qualifications Master s or PhD in Pharmacology, Pharmaceutical Sciences, or related fields. 10+ years of experience in SLR, clinical trial databases, or health economics ( 6 + years for PhD holders). Strong knowledge of clinical research, trial design, PICOS, and pharma data standards. Proficiency in R; knowledge of Python and statistical methods is a plus. Key Competencies Collaboration Communication Mentorship Adaptability Client Focus Certara bases all employment-related decision on merit, taking into consideration qualifications, skills, achievement, and performance. We treat all applicants and employees without regard to personal characteristics such as race, color, ethnicity, religion, sex, sexual orientation, age, nationality, marital status, pregnancy, physical or mental condition, genetic information, military service, or other characteristic protected by law. ","qualifications":" Master s or PhD in Pharmacology, Pharmaceutical Sciences, or related fields. 10+ years of experience in SLR, clinical trial databases, or health economics ( 6 + years for PhD holders). Strong knowledge of clinical research, trial design, PICOS, and pharma data standards. Proficiency in R; knowledge of Python and statistical methods is a plus. Key Competencies Collaboration Communication Mentorship Adaptability Client Focus Certara bases all employment-related decision on merit, taking into consideration qualifications, skills, achievement, and performance. We treat all applicants and employees without regard to personal characteristics such as race, color, ethnicity, religion, sex, sexual orientation, age, nationality, marital status, pregnancy, physical or mental condition, genetic information, military service, or other characteristic protected by law. ","responsibilities":" Database & Quality Assurance : Oversee database development, curation, QC, and deployment to platform (e.g., CODEX); ensure accurate data extraction from literature and plots; validate QC documentation and manage change impact. Technical Expertise : Conduct systematic literature reviews using PICOS, ontologies, and data standards; refine search strategies; apply clinical trial knowledge; perform R-based quality checks and exploratory analyses. Project Management : Lead planning and delivery of database products; manage resources, timelines, and change controls; ensure clear communication with clients and internal teams. Team Leadership : Mentor teams ; drive process improvement, agile practices, and learning initiatives; support hiring and onboarding. Stakeholder Collaboration : Align with clients and internal teams on expectations; review project metrics and identify enhancements. Continuous Learning : Stay current with advancements in statistics, R, SLR, and data science; contribute to innovation. " , "skills":"UNAVAILABLE" , "workHours":"UNAVAILABLE" , "jobBenefits":"" , "
Overview Certara accelerates medicines using proprietary biosimulation software, technology, and services to transform traditional drug discovery and development. Its clients include more than 2,000 biopharmaceutical companies, academic institutions, and regulatory agencies across 62 countries. We are the largest Clinical Pharmacology & Pharmacometric organization in the world, which enables us to assure that various career pathways are offered that match the ambition and personal interests of our employees! As one of Certara s divisions, we deliver value by integrating advanced simulation approaches into the most crucial drug development deliverables - to inform internal decision-making and strengthen global regulatory submissions. Leveraging our experience in working on thousands of drug development projects on behalf of hundreds of biopharma companies, we bring a track record of success and a broad range of expertise to each assignment. Responsibilities Play a key role in the development of clinical database products in various therapeutic areas like Metabolic & CV, Neuroscience, Autoimmune, Oncology, Respiratory etc., with a very high quality that support Meta-analysis (Pair wise, Network and Model based meta-analysis) Analyze and annotate the information pertaining to trial design, treatments, demographics and outcomes data (biomarker, clinical, safety and quality of life outcomes) for full time course from clinical literature (Journals, conference abstracts, Regulatory reviews etc.) Digitize the results from graphs for outcomes reported on linear, logarithmic and semi-log scales with precision Perform the above consistently with a very high quality Work with lead consultant, peer data analyst and Quality manager to understand and contribute to database rules, specifications and quality process Undergo relevant training programs (Statistics, R coding, Systematic literature review and Data analysis methods) and excel in these skill enhancement programs to grow in the organization ladder Qualifications Masters in Pharmacology or Pharmaceutics (with relevant experience), PharmaD, Clinical Practice, Masters in Public Health, and Epidemiology Minimum 1-2 years of experience in the areas of Information science, Systematic Literature review, Health-economics, and public health sectors, pharmaceutical industry experience preferred Strong knowledge of Pharmacology and clinical research is a must Knowledge of clinical development and post approval phases, PICOS approach, trial designs, Pharma Industry data standards/ontologies Knowledge of statistics, data management tools like R, is an added advantage Skills & Abilities: Comfortable in a team environment and able to communicate with and collaborate with peer scientists Excellent interpersonal skills Strong learning skills to be able to support databases in multiple disease areas Certara bases all employment-related decision on merit, taking into consideration qualifications, skills, achievement, and performance. We treat all applicants and employees without regard to personal characteristics such as race, color, ethnicity, religion, sex, sexual orientation, age, nationality, marital status, pregnancy, physical or mental condition, genetic information, military service, or other characteristic protected by law. ","qualifications":" Masters in Pharmacology or Pharmaceutics (with relevant experience), PharmaD, Clinical Practice, Masters in Public Health, and Epidemiology Minimum 1-2 years of experience in the areas of Information science, Systematic Literature review, Health-economics, and public health sectors, pharmaceutical industry experience preferred Strong knowledge of Pharmacology and clinical research is a must Knowledge of clinical development and post approval phases, PICOS approach, trial designs, Pharma Industry data standards/ontologies Knowledge of statistics, data management tools like R, is an added advantage Skills & Abilities: Comfortable in a team environment and able to communicate with and collaborate with peer scientists Excellent interpersonal skills Strong learning skills to be able to support databases in multiple disease areas Certara bases all employment-related decision on merit, taking into consideration qualifications, skills, achievement, and performance. We treat all applicants and employees without regard to personal characteristics such as race, color, ethnicity, religion, sex, sexual orientation, age, nationality, marital status, pregnancy, physical or mental condition, genetic information, military service, or other characteristic protected by law. ","responsibilities":" Play a key role in the development of clinical database products in various therapeutic areas like Metabolic & CV, Neuroscience, Autoimmune, Oncology, Respiratory etc., with a very high quality that support Meta-analysis (Pair wise, Network and Model based meta-analysis) Analyze and annotate the information pertaining to trial design, treatments, demographics and outcomes data (biomarker, clinical, safety and quality of life outcomes) for full time course from clinical literature (Journals, conference abstracts, Regulatory reviews etc.) Digitize the results from graphs for outcomes reported on linear, logarithmic and semi-log scales with precision Perform the above consistently with a very high quality Work with lead consultant, peer data analyst and Quality manager to understand and contribute to database rules, specifications and quality process Undergo relevant training programs (Statistics, R coding, Systematic literature review and Data analysis methods) and excel in these skill enhancement programs to grow in the organization ladder " , "skills":"UNAVAILABLE" , "workHours":"UNAVAILABLE" , "jobBenefits":"" , "
Overview About Certara Certara accelerates medicines using proprietary biosimulation software, technology, and services to transform traditional drug discovery and development. Its clients include more than 2,000 biopharmaceutical companies, academic institutions and regulatory agencies across 62 countries. We are the largest Clinical Pharmacology & Pharmacometric organization in the world, which enables us to assure that various career pathways are offered which match the ambition and personal interests of our employees! As one of Certara s divisions, we deliver value by integrating advanced simulation approaches into the most crucial drug development deliverables - to inform internal decision-making and strengthen global regulatory submissions. Leveraging our experience in working on thousands of drug development projects on behalf of hundreds of biopharma companies, we bring a track record of success and a broad range of expertise to each assignment. Responsibilities Play a key role in the development of clinical database products in various therapeutic areas like Metabolic & CV, Neuroscience, Autoimmune, Oncology, Respiratory etc., with a very high quality that support Meta-analysis (Pair wise, Network and Model based meta-analysis) Analyze and annotate the information pertaining to trial design, treatments, demographics and outcomes data (biomarker, clinical, safety and quality of life outcomes) for full time course from clinical literature (Journals, conference abstracts, Regulatory reviews etc.) Digitize the results from graphs for outcomes reported on linear, logarithmic and semi-log scales with precision Perform the above consistently with a very high quality Work with lead consultant, peer data analyst and Quality manager to understand and contribute to database rules, specifications and quality process Undergo relevant training programs (Statistics, R coding, Systematic literature review and Data analysis methods) and excel in these skill enhancement programs to grow in the organization ladder Qualifications Masters in Pharmacology or Pharmaceutics (with relevant experience), PharmaD, Clinical Practice, Masters in Public Health, and Epidemiology Minimum 1-2 years of experience in the areas of Information science, Systematic Literature review, Health-economics, and public health sectors, pharmaceutical industry experience preferred Strong knowledge of Pharmacology and clinical research is a must Knowledge of clinical development and post approval phases, PICOS approach, trial designs, Pharma Industry data standards/ontologies Knowledge of statistics, data management tools like R, is an added advantage Skills & Abilities: Comfortable in a team environment and able to communicate with and collaborate with peer scientists Excellent interpersonal skills Strong learning skills to be able to support databases in multiple disease areas Certara bases all employment-related decision on merit, taking into consideration qualifications, skills, achievement, and performance. We treat all applicants and employees without regard to personal characteristics such as race, color, ethnicity, religion, sex, sexual orientation, age, nationality, marital status, pregnancy, physical or mental condition, genetic information, military service, or other characteristic protected by law. ","qualifications":" Masters in Pharmacology or Pharmaceutics (with relevant experience), PharmaD, Clinical Practice, Masters in Public Health, and Epidemiology Minimum 1-2 years of experience in the areas of Information science, Systematic Literature review, Health-economics, and public health sectors, pharmaceutical industry experience preferred Strong knowledge of Pharmacology and clinical research is a must Knowledge of clinical development and post approval phases, PICOS approach, trial designs, Pharma Industry data standards/ontologies Knowledge of statistics, data management tools like R, is an added advantage Skills & Abilities: Comfortable in a team environment and able to communicate with and collaborate with peer scientists Excellent interpersonal skills Strong learning skills to be able to support databases in multiple disease areas Certara bases all employment-related decision on merit, taking into consideration qualifications, skills, achievement, and performance. We treat all applicants and employees without regard to personal characteristics such as race, color, ethnicity, religion, sex, sexual orientation, age, nationality, marital status, pregnancy, physical or mental condition, genetic information, military service, or other characteristic protected by law. ","responsibilities":" Play a key role in the development of clinical database products in various therapeutic areas like Metabolic & CV, Neuroscience, Autoimmune, Oncology, Respiratory etc., with a very high quality that support Meta-analysis (Pair wise, Network and Model based meta-analysis) Analyze and annotate the information pertaining to trial design, treatments, demographics and outcomes data (biomarker, clinical, safety and quality of life outcomes) for full time course from clinical literature (Journals, conference abstracts, Regulatory reviews etc.) Digitize the results from graphs for outcomes reported on linear, logarithmic and semi-log scales with precision Perform the above consistently with a very high quality Work with lead consultant, peer data analyst and Quality manager to understand and contribute to database rules, specifications and quality process Undergo relevant training programs (Statistics, R coding, Systematic literature review and Data analysis methods) and excel in these skill enhancement programs to grow in the organization ladder " , "skills":"UNAVAILABLE" , "workHours":"UNAVAILABLE" , "jobBenefits":"" , "