Clinical Research Associate II: Bring your career to life at Fortrea! at Fortrea

Sydney, New South Wales, Australia -

Full Time

Start Date

Immediate

Expiry Date

15 Mar, 26

Salary

0.0

Posted On

15 Dec, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Trials, Site Monitoring, Regulatory Guidelines, Data Integrity, Patient Safety, Quality Control, Adverse Event Reporting, Study Management, Travel Management, Communication, Teamwork, Problem Solving, Documentation, Time Management, Technical Skills, AI Technology

Industry

Biotechnology Research

Description

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) · Note: This role is for upcoming future opportunities that may arise at Fortrea Learn more about our EEO & Accommodations request here. Didn’t find what you were looking for? Join our Global Talent Network to stay connected with Fortrea, drive innovation and contribute to our mission of advancing life-saving therapies for patients worldwide. Follow us and stay updated about Fortrea on LinkedIn, Facebook, X, Instagram, YouTube and Glassdoor. At Fortrea, we're all about turning the “impossible” into "I'm possible." Together, we break barriers to deliver exceptional service to our patients, fueled by a shared commitment to teamwork and excellence. Regardless of your role, we're all family, working together to achieve extraordinary results. At Fortrea, your career isn't just a job – it's a journey of making the exceptional possible, every day.

Responsibilities

The Clinical Research Associate II is responsible for all aspects of study site monitoring, including routine monitoring and closeout of clinical sites, and ensuring compliance with regulatory requirements. They also prepare trip reports and track Serious Adverse Event reporting.