Our PURPOSE—to enable healthier lives everywhere, every day—is driven by a PASSION to become global champions for women’s health. We succeed by fulfilling our PROMISE to bring The Science of Sure® to life through product quality, clinical differentiation, customer relationships and our team’s talent and engagement.
Toward this end, we offer clinically proven products designed to detect, diagnose and treat disease and other health conditions that primarily affect women—earlier and more accurately than ever to provide ever greater certainty and peace of mind. This focus has fueled our long track record of innovative medical breakthroughs across many therapeutic areas—breast health, cervical health, body composition, gynecologic health, perinatal health, skeletal health and sexual health—touching the lives of more than 230 million women around the world every year. In fact, as global champions for women’s health, no company in the world has done more to fight cervical and breast cancer than Hologic—and we will continue to challenge ourselves to ensure that future generations of women have access to our life-saving innovations.
Job Summary
Under minimal to moderate supervision, the Sr Clinical Data Programmer will be responsible for performing data management and clinical data management programming activities including database build, maintaining data variable libraries, data import and export. Primary responsibilities will include programming edit checks, listings for monitoring data, progress reports, and technical solutions.
Essential Duties and Responsibilities
· Responsible for clinical data management programming activities including creating analysis datasets (as needed), clinical monitoring lists, progress reports (eg., tables, listings) to facilitate data review
· Provides oversight and standardization of externally and internally sourced data
· Implements and maintains automated data transfers
· Creates and maintains standard test cases and data for user acceptance testing
· Maintains standard edit checks, monitoring lists, data variable libraries
· Assists in data management activities and provides technical solutions across all projects
· Administers CDM applications, users accounts, and access levels required to manage clinical data including management of platform upgrades and implementation of new features
· Assists with sample collection and management database
· Recommends and implements systems and new technology to improve quality and efficiency
· Serves as liaison to core team for clinical data management and programming related issues
· Provides improvement for macro library development
· Executes projects according to timelines set by core team
· Communicates with end users to define or implement clinical data management and programming requirements for the clinical study such as data release, delivery schedules, and testing protocols
Qualifications:
· Knowledge of clinical data management principles
· Knowledge of systems used to manage clinical data, Preferred experience with IBM Clinical/Merge
· Understanding of Clinical Study process, including study design, conduct, management and data analysis.
· SAS Programming, Base SAS certification preferred
· Knowledge of programing in a relational database, preferred experience in SQL
Education
· Bachelor’s degree, preferred technology or life science related field
Experience
· 5-8 years of related experience data management or clinical data programing
Contact
Bryan Craig
Office 508.263.8362
Mobile 617.483.3525
bryan.craig@hologic.com
Toward this end, we offer clinically proven products designed to detect, diagnose and treat disease and other health conditions that primarily affect women—earlier and more accurately than ever to provide ever greater certainty and peace of mind. This focus has fueled our long track record of innovative medical breakthroughs across many therapeutic areas—breast health, cervical health, body composition, gynecologic health, perinatal health, skeletal health and sexual health—touching the lives of more than 230 million women around the world every year. In fact, as global champions for women’s health, no company in the world has done more to fight cervical and breast cancer than Hologic—and we will continue to challenge ourselves to ensure that future generations of women have access to our life-saving innovations.
Job Summary
Under minimal to moderate supervision, the Sr Clinical Data Programmer will be responsible for performing data management and clinical data management programming activities including database build, maintaining data variable libraries, data import and export. Primary responsibilities will include programming edit checks, listings for monitoring data, progress reports, and technical solutions.
Essential Duties and Responsibilities
· Responsible for clinical data management programming activities including creating analysis datasets (as needed), clinical monitoring lists, progress reports (eg., tables, listings) to facilitate data review
· Provides oversight and standardization of externally and internally sourced data
· Implements and maintains automated data transfers
· Creates and maintains standard test cases and data for user acceptance testing
· Maintains standard edit checks, monitoring lists, data variable libraries
· Assists in data management activities and provides technical solutions across all projects
· Administers CDM applications, users accounts, and access levels required to manage clinical data including management of platform upgrades and implementation of new features
· Assists with sample collection and management database
· Recommends and implements systems and new technology to improve quality and efficiency
· Serves as liaison to core team for clinical data management and programming related issues
· Provides improvement for macro library development
· Executes projects according to timelines set by core team
· Communicates with end users to define or implement clinical data management and programming requirements for the clinical study such as data release, delivery schedules, and testing protocols
Qualifications:
· Knowledge of clinical data management principles
· Knowledge of systems used to manage clinical data, Preferred experience with IBM Clinical/Merge
· Understanding of Clinical Study process, including study design, conduct, management and data analysis.
· SAS Programming, Base SAS certification preferred
· Knowledge of programing in a relational database, preferred experience in SQL
Education
· Bachelor’s degree, preferred technology or life science related field
Experience
· 5-8 years of related experience data management or clinical data programing
Contact
Bryan Craig
Office 508.263.8362
Mobile 617.483.3525
bryan.craig@hologic.com
