Study Coordinator Trainer

Covance Inc Located in: Chantilly,  Virginia
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As the #1 ranked bioanalysis services provider for drug development, Covance is seeking an Study Coordinator Trainer for their BioAnalytical group in Chantilly, VA.

This position requires 4 years of study coordinator experience in a GLP regulated lab, preferably large molecule Bioanalysis, and strong leadership skills. In this role you will be responsible for training and mentoring less experienced staff in all aspects of the study coordination position. As well as assisting in the development of departmental policies, procedures, and training manuals.

Other responsibilities Include:
•Assists SD/PI in monitoring the financial status of ongoing studies, as appropriate.
•Develops an area of expertise within the department, serves as a resource by providing individual and group training and written instructions.
•Backs up Study Coordination Supervisor by leading team meetings and taking minutes as appropriate.
•Develops new report formats as needed, including client specific formatting.
•Drives process improvement to increase the efficiency of daily/routine procedures, reporting methods, and departmental practices.
•Serves as the primary contact in communication and interaction with other departments and clients as applicable.
•Updates and maintains project tracking systems as appropriate. Provides input on new technologies, system changes, and enhancements.
•Participates in and assists Study Director/Principal Investigator (SD/PI) with pre-initiation and other study related meetings, including scheduling and leading meetings as required.
•Responsible for report preparation, including table and figure preparation.
•Assists in interpreting and evaluating data for reports.
•Maintains well documented, organized, and up-to-date study files including study schedule, protocol, and correspondence, as applicable.
•Reviews QAU report audits and submits audit responses for approval as appropriate.
•Reviews client comments and makes decisions, including appropriate study personnel as necessary, to ensure that all necessary report/raw data clarifications are completed.
•Drives report productions through finalization, including archival of data as appropriate.
•Prepares for, participates in and learns to host routine client visits.
•Manages data transfer to clients as requested.
•Monitors and schedules study phases in coordination with SD/PI.



Covance Inc. is proud to be the only drug development company with a full range of research and development services—from lead optimization, to commercialization and life cycle management. Covance, headquartered in Princeton, NJ, is the drug development business of LabCorp with global operations in more than 30 countries.


Seniority Level:
Experienced - Not Management
  Clinical Research / Affairs,  R&D / Science,  Medical Affairs
Preferred Industry Background:
Managing a team of:
Required Travel:

Base Salary:
Other Compensation: