...Study Design: The Clinical Research Associate would be expected to:
Assist with the identification and selection of investigators to... ...and guidelines in the relevant regions.
Basic...
...Align to a regulatory submission strategy in the clinical development part of the projects.
ORGANIZATION STRUCTURE
Reports to: VP - Clinical development
Relationships (Internal): Manager & all other ...
...Description
. Directs and delegates to assigned Global Trial Management staff as applicable.
. Drives study execution utilizing available... ...and costs.
. Maintains and updates dat...
...The Document Coordinator is responsible for managing and executing on centralized activities in support of global trials with an emphasis on clinical documentation.
The Document Coordinator will interact with cli...
...The Senior Manager of Biostatistics is a member of cross-functional development teams and contributes to trial design, protocol development, analysis planning, interpretation of results, and prep...
...Responsible for Clinical execution and management of all aspects of assigned clinical studies (interventional and non-interventional, from... ...and operational procedures. Might be required ...
...for CT under the EU Regulation.
Position Responsibilities
Manage the signing of clinical trial documentation such as powers of attorney, expected to be able to coordinate many signing at the same time.
Prov...
...individuals with the dedication, integrity, and creative spirit needed to thrive in our organization.
Job Description Summary
The Director, Clinical Operations, Phase 1 – India provides support through experti...
As a Clinical Research Associate you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Clinical Research Associate
Shanghai office based
Wha...
