TRABAJO CLINICAL SITE ASSOCIATE

London, basel or barcelona role type: hybrid working, #li-hybrid the associate clinical development director (oncology)  (assoc... investigator’s brochures, health...

You’ll gain exposure to various therapeutic areas and clinical study types, creating an excellent foundation for growth in global clinical operations, regulatory...

Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution... extensive experience as a clinical...

clinical project manager, study director/coordinator, clinical research associate, patient/site engagement companies) • bs or msc... at least three years experience...

Skilled in analyzing and presenting complex clinical data... monitor scientific and competitive developments to guide clinical strategy... collaborate with cross-functional...

We are looking for a clinical research associate (cra ii) to join our a-team (hybrid)... ·       activities around regulatory affairs, site activation and study-startup...

• strong knowledge of clinical trial contract management... qualifications • bachelor's degree related field req • 4 to 7 years’ relevant sponsor or clinical...

Qualifications • bachelor's degree related field req • 5 year relevant sponsor or clinical research organization clinical site contracting experience, including...

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... your responsibilities will include:...

Job description national travel required performs on-site or remote pre-study, initiation, interim, and close-out monitoring visit activities to ensure that facilities...

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

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

The objectives of the global development scientist associate director/director will be set by the global clinical product lead in agreement with global clinical...

The objectives of the global development scientist associate director/ director will be set by the global clinical product lead in agreement with global clinical...

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

Strong monitoring experience in oncological clinical trials... position summary: the manager clinical monitoring (gcm) offers an additional development path for...