TRABAJO CLINICAL TRIALS ASSOCIATE HOMEBASED

London, basel or barcelona role type: hybrid working, #li-hybrid the associate clinical development director (oncology)  (assoc... ≥ 2 years of contribution to and...

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

Collaborate with cross-functional teams to ensure high-quality execution of clinical trials... skilled in analyzing and presenting complex clinical data...

Extensive experience as a clinical research associate, with a strong understanding of clinical trial processes and regulatory requirements... what you will be doing:monitoring...

Serve as a resource for the department, ensuring scientific integrity and regulatory compliance in the application of statistical methodology to clinical trials...

We are looking for a clinical research associate (cra ii) to join our a-team (hybrid)... main responsibilities: independently manage all aspects of monitoring for...

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

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

Understanding of scientific and clinical issues related to the design and implementation of clinical trials and interpreting trial results particularly in respiratory...

Provide good clinical practice (gcp) guidance to day-to-day questions arising from clinical trials deliverables... actively leverage audit/inspection outcomes/trends...

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

Working relations:  core study team global clinical lead / clinical development lead/ early clinical lead global safety lead data monitoring committee / steering...

• indepth understanding of clinical programming and/or statistical programming processes and standards... • experience in working in cross-functional, multicultural...

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

Minimum of 5 years' experience in clinical medicine, in addition to 4 years' clinical trials experience as an investigator or in the pharma, cro, or biotech...

Excellent understanding of the clinical study process including monitoring... proven ability to lead and motivate cross-functional teams to deliver clinical trials...