Experience with edc systems like veeva vault or rave
Leadership of small programming teams
This role involves managing a team responsible for bioinformatics programming aspects of clinical trials from design through analysis and reporting
Job Summary
This role involves managing a team responsible for bioinformatics programming aspects of clinical trials from design through analysis and reporting.
The successful candidate will act as a lead programmer or project lead, overseeing both statistical and programming aspects while representing the department to clients.
Joining this global team offers opportunities for professional development, collaboration, and making a real difference in scientific breakthroughs.
Matching Summary
This role involves managing a team responsible for bioinformatics programming aspects of clinical trials from design through analysis and reporting.
Skills & Requirements
Must-have
Strong SAS programming skills
Experience with EDC systems like Veeva Vault or Rave
Leadership of small programming teams
Knowledge of ICH Statistical and reporting guidelines
Understanding of GCP and clinical trial design
Nice-to-have
Ability to adapt to changing priorities
Experience contributing to bid defenses
Willingness to present at industry conferences
Strong problem-solving and communication skills
Key Requirements
MS/MA degree in CS, Statistics, or related field with 3+ years experience
Bachelor's degree in CS, Statistics, or related field with 5+ years experience
Preferred: 6 years clinical trial experience as a statistical programmer
Preferred: At least 1 year of leadership experience