As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in ~100 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
Fortrea CRAs enjoy:
Monitoring cutting edge global clinical trials
Have experienced & supportive managers to help grow CRA knowledge and skills
Career development pathways
Opportunities to work for dedicated sponsors (FSP) and full service (FSO)
Access to AI assisted technology to ease their workload
As a CRA your responsibilities include:
Responsible for all aspects of study site monitoring including routine monitoring and closeout 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
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
Ensure the resources of the Sponsor and Fortrea 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 Fortrea travel policy
Ensure audit readiness at the site level
Prepare accurate and timely trip reports
Participate in and follow-up on Quality Control Visits (QC) when requested
Track and follow-up on Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
To join Fortrea as a CRA2 you will require:
University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure). An equivalent amount of experience can be substituted as appropriate.
Demonstrated experience of at least 18 months in onsite monitoring global clinical trials from SIV to Close-out
Understanding of local regulatory guidelines
Happy to travel interstate to attend site monitoring visits
Happy to split there time working from an office and home (Hybrid)
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Note: This role is for upcoming future opportunities that may arise at Fortrea
Learn more about our EEO & Accommodations request here.
