Clinical Research Associate Ii

The Clinical Research Associate II (CRA II) is responsible and accountable for site monitoring and site management. Has responsibility for clinical studies according to Company, and/or Sponsor Standard Operating Procedures, and local regulatory guidelines. Assures the implementation of project plans, as assigned. Act in the project role of a Local Project Coordinator or Lead CRA as assigned.

Essential Job Duties:
 The below statements are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities, skills and 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

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

 General On-Site Monitoring Responsibilities

 Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study

 Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements

 Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review

 Monitor data for missing or implausible data

 Ensure the resources of the Sponsor and Labcorp are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines, including managing travel expenses in an economical fashion according to Labcorp travel policy

 Ensure audit readiness at the site level

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

 Prepare accurate and timely trip reports

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

 Undertake feasibility work when requested

 Participate in and follow up on Quality Control Visits (QC) when requested

 Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks as instructed by supervisor

 Might be requested to work in a client facing environment

 Track and follow up on Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAE

 Independently perform CRF review; query generation and resolution against established data review guidelines on Labcorp or client data management systems as assigned by management

 Assist with training, of new employees, e.g. co-monitoring

 Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable), and may act as a local client contact as assigned

Fortrea is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

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