TRABAJO CLINICAL TRIAL SPONSOR DEDICATED

Knowledge of clinical trials - knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i...

clinical trial management and central trial oversight services provide for the regional/global coordination of clinical trial management activities for internally...

clinical trial administrator, single sponsor dedicated job overview: cta performs daily administrative activities, in conjunction with the clinical research associates...

Member of relevant clinical sub teams (cst), clinical trial teams (ctt) and an ad hoc attendee at product development team (pdt) meetings active collaboration with...

Join us in our exciting journey!! we currently require a motivated, passionate and enthusiastic clinical trials professional to join our rapidly growing clinical...

clinical research associate iqvia spain is looking for talented and motivated team member to join our sponsor dedicated team as junior cra...

Senior clinical research associate iqvia is the human data science company oriented to drive human health outcomes forward... good clinical practice (gcp) and international...

Ensure appropriate clinical trial supply plans are implemented and managed... experience in executing a wide range of clinical trial activities (from initiation...

trial start-up, maintenance and close out... our ctl's each work for a single sponsor... linical trial leaders at parexel fsp play a pivotal role in supporting,...

Ensure compliance with cdisc sdtm standards for clinical data... collaborate with cross-functional teams to support clinical data needs... additional benefits: home-based...

Experience working with clinical trial sites... this individual will report into global clinical operations, and will interface directly with the study clinical...

Senior clinical research associate will partner with the local trial manager (ltm), clinical trial assistant (cta) and clinical trial manager (ctm) to ensure overall...

Years of clinical trial monitoring experience is preferred... a minimum of 1 year of clinical trial monitoring experience is required...

The clinical research lead (crl) is responsible for the management of clinical sites being considered and/or participating in lilly clinical trials for the assigned...

You are skills set corresponding with preferentially 2+ years relevant clinical trial experience or equivalent... experienced in clinical trial management systems...