About the Job:
As a Clinical Research Assoc******** you will be responsible for makingsure that the proper standar******** protocol is being met at all termsof the clinical trial stu******** an******** are to ensure that theschedule******** are being execute******** the manner in which theyshould.
-Responsible for all aspects of study site monitoring including routinemonitoring an********-out of clinical s******** maintenance of studyf******** conduct of pre-study an******** visits; liaise with vendors;an******** ******** as assigned
-Responsible for all aspects of site management as prescribe******** theproject plans
- Recruitment of potential ******** submissions preparat********notifications to regulatory author******** translation ofstudy-relate********, organization of meetings an******** tasks asinstructe******** supervisor
- Negotiate study budgets with potential investigators an******** theCovance legal department with statements of agreements as assigned
- Complete Serious Adverse Event (SAE) report******** process productionof reports, narratives an******** up of SAEs
- Independently perform Case Report Forms (CRF) review; query generationan******** against establishe******** review guidelines on Covance orclient data management systems as assigne******** management
Requiremen********
- Minimum of four (4) years of clinical research monitoring experience(including pre-stu******** ******** routine monitoring an********visits)
- In lieu of the above re******** candidates with > four (4) yearssupervisory experience in a health care setting an******** (3) yearsclinical research experience in the pharmaceutical or CRO industries(including monitoring) may be considered
- Have a full understanding of the Serious Adverse Event (SAE)report******** process production of reports, narratives an******** upof SAEs
About Covance:
Covance Clinical Development Services is base******** anintegrate******** development services that is unique to Covance as weare one of the few truly global drug development companiespositione******** provide comprehensive clinical support fromFirst-in-Human studies through pivotal Phase III global clinical trial
At Covance, you'll discover your professional home to learn, growan********. We offer careers with a purpose in an environment thatvalues ach******** supports a balance between your personal an********l******** an******** you to make meaningful contributions to humanhealthcare.
Why Covance?
At Covance, you can make a difference by helping to deliver life-savingan********-enhancing medicines to people aroun******** world. Ourcommitment to this mission has resulte******** Covance’s impressivehistory of company stability an********. We’ve achieve******** resultsby fostering a work environment that encourages, develops an******** ourteam’s capabilities. Covance’s ongoing success offers team membersunsurpasse******** an******** development opportunities. There’s nobetter time to join us!