RemoteOtterRemoteOtterExplore 27 Remote Sdtm Jobs
ClinChoice
Join ClinChoice as a Principal Statistical Programmer / Analyst Consultant to lead programming activities for oncology clinical trials.
ClinChoice
Join ClinChoice as a Clinical R Programmer Consultant, focusing on developing SDTM and ADaM datasets remotely.
E.S
eClinical Solutions
The Senior Statistical Programmer will lead programming efforts in clinical trials, focusing on data transformation and statistical analysis.
ClinChoice
Join ClinChoice as a Principal Statistical Programmer Consultant, overseeing statistical programming deliverables in a client-facing role.
Prokidney
The Programming Contractor develops SAS programming code for statistical analysis in pharmaceutical and biotech projects.
ClinChoice
Seeking a Principal Programmer to ensure compliance with FDA and CDISC standards for clinical data submissions.
ClinChoice
Join ClinChoice as a Lead Statistical Programmer in a remote role, focusing on medical affairs and contributing to significant studies.
SERVIER MONDE
Join Servier as a Principal Statistical Programmer, leading statistical programming for clinical studies with a focus on quality and regulatory compliance.
Alira Health SAS
The Statistical Programmer II will support statistical programming activities for clinical projects, ensuring high-quality deliverables.
AbbVie
The Manager, Clinical Data and Reporting Standards is responsible for developing data and reporting standards for clinical trials at AbbVie.
AbbVie
The Senior Manager, Data Standards is responsible for developing and governing data and reporting standards for clinical trials at AbbVie.
Indero
Join Indero as an intern to assist in clinical data management for trials in dermatology.
AbbVie
AbbVie is seeking a Senior EDC Lead to drive the development of clinical data systems and standards.
AbbVie
The Senior Manager, Data Standards leads the development and governance of clinical data standards for AbbVie's clinical trials.
AbbVie
The Senior Analyst, Data Standards is responsible for developing data and reporting standards for clinical trials at AbbVie, ensuring compliance with CDISC standards.