LAVORO CLINICAL TRIAL STUDY START

clinical trial experience required (sponsor or cro)... experience with medical device clinical trials... in collaboration with the study team, leads the proactive...

Minimum 2 years of experience as a clinical study associate/clinical trial assistant or study coordinator proven organizational and administrative skills...

Strong knowledge of clinical trial processes and ich-gcp guidelines related to csr... key responsibilities: manage and oversee the organization and preparation of...

The tm clinical science group is comprised of expert clinical scientists who lead the clinical study protocol concept, design, and execution from fih through ph...

Develops expertise and understanding of clinical trials documentation, requirements, regulations, operational procedures, study file requirements, regulatory requirements...

clinical research certification (acrp or socra, clinical coordinator/cra certification) preferred... key responsibilities: study start-up and study conduct activities...

​contributes to global project and clinical team strategy and deliverables working on the asset strategy, clinical development plan, clinical protocols and other...

​ ​synopsis / protocol development, study execution, & study interpretation oversees all clinical science activities relating to the preparation / approval of synopses...

Identify and implement areas for process optimization and delivery tools to promote study team preparedness for end-to-end clinical trial delivery compliance...

O    synopsis / protocol development, study execution, & study interpretation ·        drives clinical science activities relating to the preparation / approval...

Synopsis / protocol development, study execution, & study interpretation drives clinical science activities relating to the preparation / approval of synopses, protocols...

clinical research associate (sr... and study specific training meetings... monitors activities at clinical study sites to assure adherence to gcp, ich, sops, and...

And study specific training meetings... monitors activities at clinical study sites to assure adherence to gcp, ich, sops, and study protocols...

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

This pivotal position reports directly into the study start up (ssu) country head and is responsible to lead, mentor and provide governance to the study start-up...

You will be responsible for oversight of clinical trial protocols at a site level and will collaborate closely with a local trial manager (country project manager)...

Ich-gcp) and relevant clinical r&d concepts... may perform reporting solutions role creating study specific reports translating clinical study team needs aggregating...

They are looking for a clinical affairs program manager europe... overall responsibility for design of clinical trials including protocol development, clinical trial...

Experience with sponsors, cros and outsourced clinical trial activities... solid knowledge of drug development and clinical trial processes, including related standards...

Establish and maintain methods to initiate study start up planning... use knowledge of clinical trial operations with clinical trial contracting experience preferred...