CRA - Drug Accountability (Unblinded CRA)

Labcorp is seeking an Unblinded CRA for Florida. This is a specialized CRA role which primarily focuses on drug

accountability at a site level across a range of protocols and therapeutic areas.

Essential Job Duties:

Responsible for all aspects of study site monitoring including routine monitoring and close-out of

clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with

vendors; and other duties, as assigned

l

l Responsible for all aspects of site management as prescribed in the project plans

l Travel, including air travel, may be required and is an essential function of the job.

l Prepare accurate and timely trip reports

l Review progress of projects and initiate appropriate actions to achieve target objectives

l Organize and make presentations at Investigator Meetings

l Participate in the development of protocols and Case Report Forms as assigned

l Participate in writing clinical trial reports as assigned

l Interact with internal work groups to evaluate needs, resources and timelines

l Act as contact for clinical trial supplies and other suppliers (vendors) as assigned

l Responsible for all aspects of registry management as prescribed in the project plans

l Undertake feasibility work when requested

Conduct, report and follow-up on Monitor Quality Control Visits (MQC) or Quality Control Visits

(CQC) when requested

l

Independently perform CRF review; query generation and resolution against established data

review guidelines on Covance or client data management systems as assigned by management

Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.

For more information about how we collect and store your personal data, please see our Privacy Statement .