Clinical Research Coordinator
Updated: June 05, 2024 11:17 PM GMT
![Actalent](https://www.paynhire.com/c_logo/ANd9GcSQ272kIm2WXAuf9ey0xtcUTQh2V2_Hv5W6m-XB0cM.png)
Actalent
Sydney, NSDescription:
Perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled and/or seeking enrollment in clinical studies according to the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP). Assist with daily workload planning.
RESPONSIBILITIES
Provide clinical research support to investigators to prepare for and execute assigned research studies, including:
• Review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data;
• Attend all relevant study meetings;
• Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research;
• Recruit and screen patients for clinical trials and maintain subject screening logs;
• Orient research subjects to the study, including the purpose of the study, procedures, and protocol issues such as timelines... More Detail
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