Description
Location: Los Angeles, CADuration: 12 Months
Key Summary
-Oversea lead data manager working on studies within specific drug area
-Successfully meet all deliverables, on time with a high standard of quality
-Ensure CDM procedures and processes comply and meet business requirements
-Review of all study related documents within a project area
-Communication within your assigned product teams globally and cross-functionally
-Support electronic submission activities
-Lead CDM activities for assigned project team
Necessary Experience
-Hyper linking and submission management experience, including experience with publishing software (i.s. Adobe Professional) and Inspection
-Experience is a must; related experience in CDM, working with FSP model, use/oversight of EDC systems (RAVE, InForm)
This is a great opportunity to lead CDM activities and work cross-functionally for the world's largest biopharmaceutical company as a Clinical Data Manager representing CDM internally and externally. If interest, please contact me immediately and send over your latest CV to be considered for an interview. I look forward to hearing from you.
Warm regards,
Joyce
Keywords:
Los Angeles, California, Clinical Data Manager, Clinical Data Management, RAVE, InForm, CDM, Biotechnology, Pharmaceutical, Biopharmaceutical, Global, Multinational, Adobe Professional
To find out more about Real please visit www.realstaffing.com