Clinical Research Associate II
Vor 7 Tagen
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. Benefits Monitoring cutting edge global clinical trials 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 Responsibilities 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. Qualifications 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 their 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. #J-18808-Ljbffr
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Remote Study Start-Up Associate II, Clinical Trials
vor 19 Stunden
Council of the City of Sydney, Österreich ICON Clinical Research VollzeitA leading global healthcare organization is seeking a Study Start-Up Associate II to manage clinical trial initiation from home in Australia. The successful candidate will lead regulatory document submissions, liaise with stakeholders for approvals, and support study teams on compliance. A Bachelor's degree in life sciences and 2+ years of clinical research...
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Study Start Up Associate II
vor 19 Stunden
Council of the City of Sydney, Österreich ICON Clinical Research VollzeitStudy Start- Up Associate (home-based in Australia) – Step into a pivotal Study Start-Up Associate II role within ICON’s Early Development team and help drive first-in-human research forward from the comfort of your home-office. ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive...
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Clinical Research Associate 2, Australia
vor 3 Wochen
Council of the City of Sydney, Österreich Emerald Clinical VollzeitClinical Research Associate 2, Australia Join to apply for the Clinical Research Associate 2, Australia role at Emerald Clinical . At Emerald Clinical , we are a global, full‑service Contract Research Organization (CRO) with a rich heritage in the Asia‑Pacific region. We are dedicated to advancing clinical research through scientific expertise and...
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Senior Clinical Research Associate, Australia
vor 3 Wochen
Council of the City of Sydney, Österreich Emerald Clinical VollzeitSenior Clinical Research Associate, Australia Join to apply for the Senior Clinical Research Associate, Australia role at Emerald Clinical At Emerald Clinical Trials , we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia‑Pacific region. We are dedicated to advancing clinical research through scientific...
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Senior Clinical Research Associate, Australia
vor 2 Wochen
Council of the City of Sydney, Österreich Emerald Clinical VollzeitSenior Clinical Research Associate, Australia Join to apply for the Senior Clinical Research Associate, Australia role at Emerald Clinical Trials. Emerald Clinical Trials is a global, full‑service Contract Research Organization (CRO) with a rich heritage in the Asia‑Pacific region. We are dedicated to advancing clinical research through scientific...
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Senior Clinical Research Associate, Australia
Vor 7 Tagen
Council of the City of Sydney, Österreich Emerald Clinical VollzeitSenior Clinical Research Associate, Australia Join to apply for the Senior Clinical Research Associate, Australia role at Emerald Clinical At Emerald Clinical Trials, we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise...
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Clinical Site Associate
Vor 7 Tagen
Council of the City of Sydney, Österreich ICON Clinical Research VollzeitClinical Site Associate - Office based in Sydney ICON plc is a world‑leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Clinical Site...
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Council of the City of Sydney, Österreich Emerald Clinical VollzeitA global clinical research organization is seeking a Clinical Research Associate 2 (CRA2) to coordinate and manage clinical trials. The ideal candidate will have a background in life sciences and 2-5 years of experience in clinical trials monitoring. In this role, you will be responsible for site selection, budget negotiations, and ensuring compliance. Join...
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Senior Clinical Research Associate – Australia
vor 2 Wochen
Council of the City of Sydney, Österreich Emerald Clinical VollzeitA leading Contract Research Organization in Australia is looking for a Senior Clinical Research Associate to manage clinical trials and ensure compliance with regulations. You will be responsible for site selection, trial coordination, and ensuring participant safety. The ideal candidate will have a relevant degree and at least 4 years of experience in...
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Clinical Recruitment Associate
vor 2 Wochen
City of Melbourne, Österreich Pinnacle Clinical Research VollzeitPosition: Clinical Recruitment Associate Location: Springfield, NJ Job Id: 529 # of Openings: 1 Come join our team and make a difference as we blaze the way into the future of medical discovery through world-class clinical research. At Pinnacle Clinical Research, we are committed to driving innovation and advancing medical knowledge. Through our rigorous...
