Job Description
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
Join Us as a Central Review Manager – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
As part of our global team, you’ll have the opportunity to perform centralized report review and approval of PSA, SI, ME, and CO reports on assigned projects in accordance with procedural documents and guidelines.
What You’ll Do:
• Performs review of clinical monitoring visit reports for allocated projects ensuring consistency across protocols and/or regions and escalates any protocol, site, and/or CRA issues or trends noted during the report review process to CL.
• Liaises with clinical monitoring staff for prompt trip report review submission and approval as per the stipula...
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
Join Us as a Central Review Manager – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
As part of our global team, you’ll have the opportunity to perform centralized report review and approval of PSA, SI, ME, and CO reports on assigned projects in accordance with procedural documents and guidelines.
What You’ll Do:
• Performs review of clinical monitoring visit reports for allocated projects ensuring consistency across protocols and/or regions and escalates any protocol, site, and/or CRA issues or trends noted during the report review process to CL.
• Liaises with clinical monitoring staff for prompt trip report review submission and approval as per the stipula...