Associate, Study Management II//CTM II
Core
Execute elements of clinical studies in compliance with quality standards and support the Study Project Manager in leading cross-functional teams.
Role type
Associate Study Manager (Clinical Trial Management)
Builds
Clinical study blueprints, protocols, and associated systems/documents
Domain
Pharmaceutical clinical research
Deliverable
client delivery
Required skills
Clinical study execution, cross-functional team support, study status reporting, vendor management, training development, issue resolution, process improvement
Preferred skills
Analytical thinking, critical thinking, communication
Technologies
CTMS, eCRFs, IRT, CSR
Responsibilities
Prepare Clinical Study Team meetings (Agenda/Minutes), update cross-functional team and stakeholders on study status, support development of clinical study blueprint/protocol and documents, manage external vendors, generate study-related training, identify and resolve study issues, participate in process improvement initiatives
