...Job Description
Role Summary
The Site Care Partner is the main Pfizer point of contact for investigative sites throughout a study... ...Pfizer at government presentations and also a...
• Close interaction and collaboration with study team lead and study team members during study lifetime, Review of vendor related protocol sections during protocol development. Collaborate with Vendor startup manager to the development of Study Speci...
...the impact you could have.
Job Purpose:
The SSO Clinical Project Manager (CPM) is accountable for the day-to-day planning, executing... ...and diverse teams representative of the patien...
...The Lead Data Manager (LDM) within the ERGOMED Data Management (DM) department is responsible for providing oversight of all DM parts of a project from study start-up to database lock by working in a collaborative t...
...The Clinical Project Leader (CPL) / Local Study Manager (LSM) is part of the Clinical Study Unit (CSU), and is accountable for the strategic... ...area in terms of study management and conduc...
...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...
Designation: Clinical Data Management
Full Time Opportunity
Location: Multiple
Job Description:
- Understand and follow study start-up, conduct, and close out activities per the standard process, which will be made known to Service Provid...
...members during study lifetime, Review of vendor related protocol sections during protocol development. Collaborate with Vendor startup manager to the development of Study Specification Worksheet (SSW) to facilitate ...
