Senior Statistical Programmer - Real World Evidence and Epidemiology
Cytel, Cambridge, Massachusetts, us, 02140
Join our dynamic team as a Senior Statistical Programmer, where you will play a crucial role by:
Supporting the Epidemiology team through the preparation of Real World Data, providing strategic insights into data analytics, and assisting stakeholders with diverse epidemiological analyses.
Conducting detailed statistical analyses under the supervision of experienced epidemiologists and statisticians, focusing on data coding, algorithm development, dataset integration, and the application of robust statistical software.
Enhancing our statistical programming capabilities to innovate processes related to data standardization, visualization, and reporting for observational data.
Collaborating effectively with Medical Affairs, Global Patient Safety and Risk Management, and Clinical Development on observational studies and regulatory assessments.
Building and nurturing strong partnerships with internal and external stakeholders in conjunction with Epidemiologists.
Managing and prioritizing work across multiple projects efficiently to meet diverse stakeholder needs.
Ensuring clear communication for successful and timely project execution.
Applying your technical expertise and problem-solving skills in a proactive manner to support our goals.
Your key responsibilities will include: Assisting in the development of study protocols and analytical plans that leverage extensive Real World Data sources.
Partnering with data vendors to obtain relevant data extracts that align with research study protocols.
Creating analytical databases from data extracts to streamline the data analysis process effectively.
Executing analyses that adhere to established methodologies articulated in study protocols.
Generating comprehensive tables and figures for presentations aimed at researchers, clients, and for study documentation.
Presenting findings in an engaging and coherent manner to both internal teams and external clients.
Assisting in the creation of study reports and other essential documentation.
Possibly overseeing team members as our team evolves.
We seek candidates who have: A Master's degree or PhD in a relevant field such as epidemiology, biostatistics, statistics, bioinformatics, or economics, with at least 5 years of experience in Real World Evidence analytics within the pharmaceutical sector, CRO, or academia.
Intermediate to expert skills in SQL, complemented by expertise in SAS or R programming.
A strong understanding of Real World Evidence data sources including Optum, Truveta, and UK Biobank; experience with clinical trial or registry data will be a plus.
Familiarity with relational databases and comprehensive knowledge of claims and ancillary file formats.
Expertise in applied statistical methods, including various regression analyses and survival analyses.
Strong project management abilities; capable of balancing multiple projects and meeting deadlines.
Confidence in engaging with both internal and external stakeholders.
Excellent written and verbal communication skills, with the ability to effectively summarize and present critical insights.
Cytel Inc. is committed to being an Equal Employment / Affirmative Action Employer. All applicants are considered for positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law.
Conducting detailed statistical analyses under the supervision of experienced epidemiologists and statisticians, focusing on data coding, algorithm development, dataset integration, and the application of robust statistical software.
Enhancing our statistical programming capabilities to innovate processes related to data standardization, visualization, and reporting for observational data.
Collaborating effectively with Medical Affairs, Global Patient Safety and Risk Management, and Clinical Development on observational studies and regulatory assessments.
Building and nurturing strong partnerships with internal and external stakeholders in conjunction with Epidemiologists.
Managing and prioritizing work across multiple projects efficiently to meet diverse stakeholder needs.
Ensuring clear communication for successful and timely project execution.
Applying your technical expertise and problem-solving skills in a proactive manner to support our goals.
Your key responsibilities will include: Assisting in the development of study protocols and analytical plans that leverage extensive Real World Data sources.
Partnering with data vendors to obtain relevant data extracts that align with research study protocols.
Creating analytical databases from data extracts to streamline the data analysis process effectively.
Executing analyses that adhere to established methodologies articulated in study protocols.
Generating comprehensive tables and figures for presentations aimed at researchers, clients, and for study documentation.
Presenting findings in an engaging and coherent manner to both internal teams and external clients.
Assisting in the creation of study reports and other essential documentation.
Possibly overseeing team members as our team evolves.
We seek candidates who have: A Master's degree or PhD in a relevant field such as epidemiology, biostatistics, statistics, bioinformatics, or economics, with at least 5 years of experience in Real World Evidence analytics within the pharmaceutical sector, CRO, or academia.
Intermediate to expert skills in SQL, complemented by expertise in SAS or R programming.
A strong understanding of Real World Evidence data sources including Optum, Truveta, and UK Biobank; experience with clinical trial or registry data will be a plus.
Familiarity with relational databases and comprehensive knowledge of claims and ancillary file formats.
Expertise in applied statistical methods, including various regression analyses and survival analyses.
Strong project management abilities; capable of balancing multiple projects and meeting deadlines.
Confidence in engaging with both internal and external stakeholders.
Excellent written and verbal communication skills, with the ability to effectively summarize and present critical insights.
Cytel Inc. is committed to being an Equal Employment / Affirmative Action Employer. All applicants are considered for positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law.