TRABAJO CLINICAL ASSOCIATE SPONSOR DEDICATED

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

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

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

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

• superior clinical research operational knowledge... clinical trial management and central trial oversight services provide for the regional/global coordination...

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

Demonstrated capability to consistently deliver clinical trials...   description: a senior clinical research associate (senior site manager) serves as the primary...

Member of the medicine development team and of clinical study team(s)... as a specialized biopharmaceutical company, we are dedicated to rare diseases...

As a specialized biopharmaceutical company, we are dedicated to rare diseases... member of the medicine development team and of clinical study team(s)...

Arranges for the appropriate destruction of clinical supplies... 1-2 years of clinical trial monitoring experience is preferred... a minimum of 1 year of clinical...

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

As an associate clinical specialist, you will provide expert clinical products and technical assistance to physicians and ep lab staff... exhibit an ability to troubleshoot...

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

Escalate changes that fall outside the documented “fall-back” parameters, if available to the sponsor or to clinical site agreement manager as appropriate...