AMAZING opportunity for a consultant specialized in data analytics of Real World Evidence using SAS!
If you looking for...
An opportunity to apply your PhD and the experience you've gained in Real World Evidence?
The opportunity to work closely with a tight knit team of Industry SMEs and gain incredible professional exposure?
The opportunity to review and analyze retrospective RWE and offer strategic holistic solutions to clients?
Then please consider applying to the Senior Associate Real-World Data & Analytics on the PAREXEL Access Consulting Team!
PAREXEL Access Consulting is seeking to find an experienced and passionate consultant with an interest in health economics. The generation of new clients, the ongoing relationship management with existing clients and the successful management of projects are essential to the growth, security and prosperity of the company. The candidate will be expected to play an instrumental part in the ongoing development and direction of real world evidence studies, being encouraged to bring with them ideas and aspirations to drive forward the research studies and the business.
The Senior Associate Real-World Data & Analytics is an extremely exciting and high profile position within one of the fastest growing organizations in the field! The role will offer tremendous exposure and learning opportunities. Additionally, there will be considerable scope for a high performing individual to implement their ideas for growth into the company in a creative and collaborative atmosphere.
Role objectives and aims: •Apply data analytics to support research projects and collaborations within the team. This will include conducting statistical analyses, creating analytic datasets, and performing quality control. •Define analytical variables collaboratively with research scientists and biostatisticians. • Perform analytical tasks using SAS and other analytical tools. • Follow comprehensive quality checking and validation processes. • Create and maintain documentation to document process and data quality issues. •Perform other related duties incidental to work described herein. •Potential for opportunities in database administration including acquisition of potential data sources and follow-on steps of cleaning, aggregating and importing data from a variety of sources; and analyzing data quality and recommendations for remediation of quality issues.
Ideal candidate should possess:
• A Master’s degree or PhD in the area of outcomes research, epidemiology, biostatistics, statistics, health services research, or a related field. • A minimum of 2-3 years’ experience working with large relational databases, processing large administrative healthcare datasets (medical and pharmacy claims), and or clinical databases (Electronic Health Records), creating final analytical databases, conducting secondary data analyses, and developing research study designs. • The candidate should possess strong skills in SAS programming. The ideal candidate will also have experience and training in statistical modeling, and development of programs and macros. Demonstrated evidence of publications will be viewed favorably. Recent Pharmaceutical / CRO experience preferred. • Experience in health economics specialized in Real World Evidence. • Good presentation skills • Strong project management skills • A high degree of written accuracy and attention to detail • Strong communication skills, especially in the relaying of technical information and project concepts. • Flexible, determined and self-motivated
PAREXEL is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
Telecommuting is allowed.
Internal Number: 50074BR
Headquartered near Boston, Massachusetts, PAREXEL has offices in 84 locations in 51 countries with capability to support our clients in over 100 countries around the world, and has approximately 18,900 employees.
We provide the most comprehensive drug development capabilities of any CRO worldwide. Our global regulatory expertise, Phase I-IV clinical research services, integrated eClinical technologies, and advanced commercialization services all work together to move you through the development journey more smoothly and cost-effectively from beginning to end.