LAVORO CLINICAL TRIAL MANAGER CRO

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

• 6-8 years clinical trial management experience in the pharmaceutical industry or cro... global trial delivery manager services provide for the global coordination...

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...

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

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

Study documents managed through edms) and supports the cpm in ensuring the compliance of the clinical trial with internal sops and applicable regulations - prepare...

Senior regulatory affairs manager (remote - eu/uk)  are you a regulatory expert with a passion for oncology clinical trials? join a global cro with over 40 years...

The global clinical operations program director (gpd) is a core global role within the clinical operations function of late stage r&d (biopharmaceuticals and oncology)...

Gra, etc) and external key opinion leader/ investigator    management of the interaction with external cro and consultants to support the clinical pharmacology...

• experience in clinical research experience in the pharmaceutical industry or cro... •   ensures study (s) compliance by maintaining and updating trial management...

Strong knowledge of ich-gcp, clinical trial lifecycle, regulatory requirements, and cro/vendor management... experience required at least 8–10 years of experience...

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

Drive negotiation and administration of master clinical trial agreements... accountabilities: manage negotiations, finalization and administration of master clinical...

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

•          6 years of relevant experience in clinical trial operations in the pharmaceutical industry, cro, or equivalent related experience required, as deemed...

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

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

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