RemoteOtterRemoteOtterExplore 18 Remote Sdtm Jobs
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.
AbbVie
AbbVie is seeking a Senior Analyst for Clinical Data Systems to enhance clinical trial data management and ensure project delivery.
ClinChoice
Join ClinChoice as a Senior Principal Statistical Programmer and contribute to impactful clinical research.
AbbVie
Lead the development and maintenance of electronic data capture systems for clinical trials.
A.B
Arcus Biosciences
Join a growing Biometrics team as a Senior Clinical Programmer, responsible for data management and programming in clinical trials.
Welcome to the Tarsanet Internal Career Center!
The Associate Director, Clinical Data Management leads data management for clinical studies, ensuring data integrity and quality.
Recursion
Join Recursion as an Associate Director/Director of Statistical Programming to lead statistical programming efforts in clinical development.
BridgeBio
Lead statistical programming activities for clinical trials at QED Therapeutics.
C.P
Centessa Pharmaceuticals
The Director/Sr. Director in Statistical Programming will lead statistical programming efforts and contribute to clinical development in a remote role.
D.S
Daiichi Sankyo
The Associate Director will lead statistical programming efforts to support clinical trials and regulatory submissions in the pharmaceutical industry.