Data Analyst 2

Certara; Secunderabad; On-site; INR 500,000 - 700,000; Full time

Job summary

Certara seeks a skilled professional to interpret clinical trials data and contribute to database products used in meta-analyses across therapeutic areas such as Metabolic & CV, Neuroscience, Autoimmune, Oncology, and Respiratory.

The role requires strong pharmacology knowledge, experience with systematic literature review, and familiarity with R; training in statistics and data analysis will be provided to advance in the organization.

Qualifications

• Masters in Pharmacology or Pharmaceutics with relevant experience.
• Pharma D, Clinical Practice, or MPH with epidemiology focus is acceptable.
• Experience in information science, systematic literature reviews, health economics, or pharma industry is preferred.
• Knowledge of pharmacology and clinical research is essential.
• Understanding of clinical development phases and data standards is advantageous.

Responsibilities

• Develop and contribute to clinical database products across therapeutic areas with high quality for meta-analysis.
• Annotate trial design, treatments, demographics, and outcomes from literature for data integration.
• Digitize results from graphs on various scales with precision.
• Collaborate with lead consultants, data analysts, and quality managers to ensure database rules and quality processes.
• Engage in training programs (Statistics, R, systematic reviews, data analysis) to grow professionally.

Skills

Team collaboration

Communication

Interpersonal skills

Learning agility

Education

Masters in Pharmacology

Pharma D

Masters in Public Health

Epidemiology

Tools

R

Job description

About Certara

Certara accelerates the potential of bringing medicines to market and to patients using biosimulation software, technology, and services to transform traditional drug discovery and development. Our clients include more than 2,400 biopharmaceutical companies, academic institutions, and regulatory agencies across 70 countries.

Overview

About Certara

Certara accelerates the potential of bringing medicines to market and to patients using biosimulation software, technology, and services to transform traditional drug discovery and development. Our clients include more than 2,400 biopharmaceutical companies, academic institutions, and regulatory agencies across 70 countries.

Our goal is to enable the life sciences industry’s use of data, modeling, and analytics to make better decisions across the various phases of discovery and drug development.

Our software and scientists incorporate modern advances in scientific understanding, drug development experience, data analysis, and AI resulting in significant opportunities to decrease the cost and increase the probability of success for new drug approval and commercialization.

This job entails interpretation of Clinical trials data across various therapeutic areas and actively contribute to the development of database products that support informed decision making at various stages of clinical development and post approval phases using modelling and simulation approaches.

This job necessitates a profound knowledge of pharmacology and clinical research, experience in development/process of clinical databases for conducting systematic literature review and meta-analysis (pair wise, network and model based meta-analysis).

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), 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

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.