The role serves as a lead Clinical Programmer responsible for managing multiple project timelines and delivering software solutions for drug development
Job Summary
The role serves as a lead Clinical Programmer responsible for managing multiple project timelines and delivering software solutions for drug development.
Candidates will act as a senior technical subject matter expert supporting clinical programming staff on tools like Medidata Rave, Oracle Inform, and SAS.
Syneos Health offers a supportive culture with career development opportunities, peer recognition, and a commitment to building an inclusive workplace.
Matching Summary
The role serves as a lead Clinical Programmer responsible for managing multiple project timelines and delivering software solutions for drug development.
Skills & Requirements
Must-have
6+ years DM SAS Clinical Programming experience
SAS listings and macro creation
Data imports and acquisition
Study build and SAS mapping
Electronic Data Capture (EDC) support
Oversight of 4-5 concurrent studies
Nice-to-have
Preferred Lead experience
Excellent communication skills
Experience in matrix-structured environment
PL/SQL, C#, or VB programming knowledge
Ability to travel up to 25%
Key Requirements
Bachelor's degree preferred
Base and Advanced SAS certification preferred
Minimum 6 years of DM SAS Clinical Programming experience