LAVORO CLINICAL MANAGER

Summary clinical trial supply manager (ctsm) defines and executes an optimal clinical trial supply strategy for a clinical trial including effective risk management...

Accountabilities: work with gcsc planning function to interpret clinical trial drug requests and clinical protocols and to develop supply packaging strategies, timelines...

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

External collaborators include academic and clinical researchers... understanding of clinical trial design, execution, and regulatory requirements (e...

We’re looking for a  senior regulatory affairs manager  to lead and support regulatory activities across europe... senior regulatory affairs manager (remote - eu/uk) ...

Nota: se percepisci la naspi puoi accedere al voucher naspi unopportunit pensata per chi desidera aggiornare le proprie competenze e facilitare il reinserimento...

Ensure that clinical pathways activities align with regulatory standards and internal policies... experience with pathway modelling tools, health economics software...

• superior clinical research operational knowledge... global trial delivery manager services provide for the global coordination of clinical trial management activities...

clinical expertise demonstrate a deep understanding of clinical science supporting our products in electrophysiology & gather/develop data intelligence in our...

clinical research and program management experience working with clinical programs within medical affairs, clinical research, regulatory, cmc or other drug development...

Communication primary communication point for project teams and company departments with regard to clinical data management communication line for clients/vendors...

Excellent knowledge of the clinical trials settings... support the cross-functional team working on clinical trials transparency, with a particular focus on content...

Solid knowledge of good clinical data practices, gcp and regulatory requirements... minimum 5 years of experience in clinical data management in cros or pharmaceutical...

May directly support clinical operations program leads in day-to-day activities for complex and/or business-critical clinical studies (including providing clinical...

You will be a part of the clinical it team and report to the clinical it manager responsible for coordinating both upstream (the product) and downstream (the go...

Ecrts, iss, ise, bimo, p21 checks) and providing support for regulatory questions; lead and organize study level programming and oversight activities for analysis...

Ensure alignment with clinical needs and regulatory requirements... strong understanding of molecular imaging technologies clinical workflows and healthcare purchasing...

With global clinical research locations all over the world opis offers a full range of integrated clinical research services as scientific advice medical writing...