As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
Senior Analyst, Real World Evidence (RWE) (Remote): This is a permanent, remote opportunity that can be worked from anywhere in U.S #LI-REMOTE
Are you ready to discover your extraordinary potential at Fortrea? A career here provides the unique chance to create a lasting impact and difference in patients’ lives. Joining our team will offer you a rewarding career, an opportunity to work in a high-energy, innovative & collaborative workplace, along with access to comprehensive benefits.
Job Overview:
- Providing programming and analysis support for Real World Evidence projects for Fortrea clients.
- • Having good understanding of the various sources on Real World Data to be used in the analysis.
Essential Job Duties:
- Provide programming support for analysis of real-world data from different sources including medical and pharmacy claims data, hospital data, electronic medical record data, and prospective observational study data.
- Contribute to development of programming specifications for conducting the analysis using requirement details and source data.
- Develop/validate analysis datasets from a variety of file and formats from either internal or external vendors as well as using diverse collection of data files in terms of the type, data format and size.
- Develop/validate graphs and tables primarily for exploratory investigations with analysis requirements that may change throughout the life of the project.
- Ensure excellence in the programming of analysis ready datasets, tables, listings, and figures, and associated validation work.
- Develop and maintain required documentation for the assigned deliverables.
- Communicate accurate and timely status updates to project lead and other project team members.
- Present and share knowledge at department meetings.
- Identify processes within programming that will increase productivity, quality, and efficiency.
- And all other duties as needed or assigned.
Qualifications (Minimum Required):
- Bachelor’s or Master’s degree in Computers, Engineering, Statistics, Health Informatics, Life Sciences, Mathematics, Economics, or Econometrics.
- Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
Experience (Minimum Required):
- Typically, 3-5 years of RWE analysis experience in the CRO or Pharmaceutical Industry, or an equivalent combination of education and experience to successfully perform the key responsibilities of the Job.
- Experience in handling data from EHR/Claims databases (Optum, Marketscan, Flatiron etc.) is required.
- Proficiency in SAS and SQL programming.
Preferred Qualifications Include:
- Experience in programming languages such as R and Python.
- Experience with handling big data, non-standard/new data, and complex data.
- Expertise in creating various types of graphs for data presentation.
- Strong analytical mindset and logical thinking capability.
- Positive attitude and willingness to learn and contribute to a team setting and communicate effectively within the team environment.
- Experience in working with real-world data from health insurance claims, retrospective analyses, manual chart reviews, prospective observational studies, and pragmatic clinical trials.
- Good understanding of advanced statistical and econometric methods in theory and practice.
- Ability to take detailed RWE study results and communicate them in a clear, non-technical manner to internal cross-functional teams, using language that resonates with the teams, while maintaining the integrity of key findings.
- Ability to work effectively in a constantly changing, diverse and matrix environment.
US Pay Range: $80,000 - $100,000 USD
Benefits: All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), ESPP, Paid time off (PTO) or Flexible time off (FTO), Company bonus where applicable. For more detailed information, please click here. Application deadline is October 11, 2024.
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
Fortrea is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
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