TRABAJO CLINICAL CONTRACTS SPECIALIST SPONSOR

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

Escalate changes that fall outside the documented “fall-back” parameters, if available to the sponsor or to clinical site agreement manager as appropriate...

Arranges for the appropriate destruction of clinical supplies... 1-2 years of clinical trial monitoring experience is preferred... a minimum of 1 year of clinical...

Previous experience in clinical trial regulatory submissions... knowledge of the principles, methods, and procedures of clinical research...

Experienced in clinical trial management systems & tmf management experienced in contracts management and negotiation proficient in english language...

• interfaces with data management centre and/or data management, global clinical solutions representatives to facilitate the delivery of study related documents/material...

Iqvia is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry...

Maintain oversight of contracts and quality agreements on loc level... how you will contribute: responsibilities cover gxp-regulated activities including in-country...

clinical study protocol (csp) through to clinical study report (csr)) in accordance with relevant az sops... experience in all phases of a clinical study lifecycle...

Good understanding of clinical trial contract management...   qualifications bachelor's degree related field req 5-year relevant sponsor or clinical research...

Good understanding of clinical trial contract management... qualifications bachelor's degree related field req 5-year relevant sponsor or clinical research organization...

Knowledge and experience experience in clinical medicine (general or specialist qualifications) with a specialty in hematology and hematopoietic stem cell transplantation...