TRABAJO CLINICAL STUDY MADRID, MADRID

Deep knowledge of international clinical trial regulations (ich-gcp, fda, ema)... supervise clinical trial monitoring, investigational product handling, and patient...

Excellent understanding of the clinical study process including monitoring... reports study progress/update to the global study associate director/ global study...

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

Implementation of study amendment-and changes in study related processes)... knowledge of clinical trials - knowledge of clinical trial conduct, and skill in applying...

Day to day responsibilities will include: support clinical research studies and maintain a safe study environment according to health and safety policies under the...

The study project manager ii achieves these objectives by bringing scientific acumen, strategic asset level thinking, innovation, expertise in clinical study operations...

clinical trial manager icon plc is a world-leading healthcare intelligence and clinical research organization... collaborate with cross-functional teams to establish...

This is your opportunity to shape how we operate, influence leadership decisions, and help deliver better outcomes for patients through smarter, more agile clinical...

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...

In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; e... the obesity medical strategy lead is a subject matter expert...

The cardiovascular medical strategy lead is a subject matter expert with experience in clinical research and clinical trials who will be a champion for cardiovascular...

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

• superior clinical research operational knowledge... • 6-8 years clinical trial management experience in the pharmaceutical industry or cro...

What you will be doing: monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and good clinical practice (gcp) standards...

Preferred:previous experience as in-house cra, study start-up specialist, or regulatory specialist, clinical research coordinator... support enrollment, site communications...

What you will be doing: supporting in-house cra activities related to the day-to-day running of clinical trials as defined by the study budget...