Skills

Communication Leadership Python Data Analysis Data Mining Risk Management Research Literature review Regression Programming Analytics Data Science Mathematics

Job Specifications

Title: Associate Director, Epidemiology Analytics

12 month contract

Remote - US Based in EST - must be able to come to client site in NJ 1 x quarter

Pay Rate $90/hr - $93/hr

Contracting with this sponsor client offers a strong mix of professional growth, flexibility, and purpose. As a global pharmaceutical leader known for innovation in oncology, cardiovascular medicine, and antibody-drug conjugates, they provide the opportunity to work on cutting-edge projects that make a real impact on patient lives. Competitive pay, flexible schedules, and the chance to collaborate with international teams, gaining valuable global experience. If you are interested in a rewarding contract opportunity to contribute meaningfully while growing professionally, apply now!

RESPONSIBILITIES

Provide data management of diverse data (e.g., real-world setting and clinical trial) to set up epidemiologic data sets for various approaches, quantitative epidemiologic data analysis, interpretation of results, visualization of results, and generate manuscripts to disseminate findings
Conduct statistical analyses for epidemiological research and safety queries, including but not limited to:

o Descriptive summary and multivariable regression o Exploratory analysis for safety endpoints in clinical trial data

o Setup and analysis of case-control and cohort study designs o Signal detection analysis in spontaneous reports (e.g., FAERS, EVDAS)

o Signal detection/evaluation analysis in RWD

o Data mining (including free-text mining of unstructured data fields) using diverse data sources and methods

o Development of automation platform (e.g., R Shiny App)

o Literature review and meta-analysis

Collaborate with cross-functional teams to evaluate and manage adverse events and risks associated with pharmaceutical products. Participate in cross-functional meetings and provide input and guidance as needed. Participate in the preparation and submission of regulatory documents related to drug safety.
Maintain and manage project plans to provide deliverables on time.
Collaborate with global epidemiology teams to ensure consistency and quality in safety reporting and processes. Maintain compliance with all applicable regulations and guidelines related to pharmacovigilance and drug safety. Stay informed about emerging safety issues and contribute to the development of risk management strategies
Mentor and provide guidance to junior team members.

Skills:

Experience in epidemiologic methods and data analysis (pharmaceutical industry in safety or associated service provider experience is preferred)
Proficiency with programming in R, SAS, or Python for data mining and epidemiologic analysis
Strong written, oral and electronic communication skills
Excellent leadership skills, with the ability to work effectively in a collaborative team environment
The ideal candidate will have a strong background in both biostatistics and epidemiology (or other medical fields)

Education: * Master's degree (with 7+ years of experience) or PhD (with 4+ years of experience) in Biostatistics, Data Science, Statistics, Applied Mathematics, Epidemiology or related field

Ref: #568-Clinical

About the Company

At Joule, we believe our world is filled with possibilities - where character, integrity, and commitment drive our purpose. For over 30 years, Joule has been a trusted partner to industry-leading clinical, scientific, and healthcare organizations by providing innovative workforce solutions and delivering top talent. Operating at the forefront of the life sciences arena, Joule's relentless approach enables our clients to rapidly and effectively execute critical initiatives and major projects. Joule is a System One division. Know more