Sr Analyst/Consultant, RWDS Job in Certara EMEA

  • Full Time
  • EMEA

Website Certara

This Job Listing is about Certara in EMEA 2022

About the job

At Certara, we accelerate medicines to patients by partnering with life science innovators.

Our Integrated And Proprietary End-to-end Platform With Biosimulation, Regulatory Science, And Market Access Solutions Combined With Our Strong Team Of Scientists And Subject Matter Experts Enable Our Clients To Have

In the past 6 years, over 90% of companies that received new drug approvals by the FDA used our software or services.

  • informed decision-making & reduced clinical trial burden
  • higher R&D productivity
  • improved patient outcomes & increased patient access to medicines
  • accelerated regulatory approval

Certara is a global team that fosters and nurtures a diverse and inclusive culture. We are proud to be an Equal Opportunity Employer. The collective sum of our individual differences, life experiences, knowledge, innovation, self-expression, and unique capabilities and talent represents a significant part of our culture, our reputation and our achievement.

Together with our partners, we use biosimulation and technology-enabled services to transform drug discovery and development across all therapeutic areas and innovative therapies.

Job Overview

This is a great opportunity for an early career Epidemiologist/Pharmaco-Epidemiologist/Public Health professional to join a team of highly skilled epidemiologists, statisticians, health economists and consultants. The successful candidate will work closely with other senior scientific staff within the company. This position will allow the Senior Analyst/ Epidemiologist to deepen his/her skills by writing protocols for observational studies using a variety of healthcare databases, primary and secondary data collection, as well as providing scientific and other technical input during conception, conduct and delivery of various research projects.

Main Tasks & Responsibilities

  • Support RWDS project teams and be accountable to the project manager/director for those projects
  • Summarize and synthesize a wide range of medical and statistical information, including disease specific and pharmaceutical product research
  • Develop an understanding of Regulatory/HTA requirements for RWE, at least in the European and/or North American context
  • Support development of study documents (eg. protocols, analysis plans, reports, posters, manuscripts) under guidance from scientific team members and project manager/s
  • Liaise and manage processes with ethics committees, application committees and other relevant stakeholders to support acquisition of data for studies
  • Interpret and communicate the results of clinical/observational studies, health economic models (cost-effectiveness and budget impact) and statistical analyses
  • Undertake primary and secondary research initiatives including the retrieval and analysis of data, competitive product pipeline information, epidemiology trends, etc. according to needs of the project
  • Participates in production of reports, presentations and publications.
  • Critically analyzes data (presents results and provides internal data analysis, both qualitative and quantitative) and provides strategic thinking with respect to interpretation of results
  • Interact with and foster relationships with existing network of scientific/clinical/payer experts and data providers
  • Liaise with other consultants assigned to the project to ensure quality delivery of the project
  • Support senior personnel with activities required for business development from time to time
  • Align with and work within the framework of SOPs for data governance with respect to projects led

Required Qualifications / Experience

  • Minimum of Master’s Degree in Epidemiology, Public Health, Medicine or other related field
  • At least 2 years relevant post-graduate work experience preferred

Required Skills

  • Professional proficiency in English, written and spoken
  • Experience designing/writing protocol for database or other observational studies
  • Ability to work both independently and as part of the team
  • Ability to effectively prioritize and manage multiple tasks and projects

Other Information

This position can be office based or work-from-home in the UK, EU, Canada or USA.

Number of Employees Supervised: None

Percentage of Travel Required: 0-10% travel

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.


Company: Certara

Vacancy Type: Full-time · Associate 

Job Location: EMEA

Application Deadline: N/A

Apply Here