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), Pharma D, 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
