A Clinical Research Associate (CRA) is a professional who plays a crucial role in the field of clinical research. Their primary responsibility is to ensure that clinical trials are conducted in compliance with regulatory guidelines, protocols, and good clinical practice (GCP) standards. Here are some of the key tasks and responsibilities of a Clinical Research Associate:
Study Start-up: CRAs contribute to the initiation of clinical trials by assisting with site selection, conducting pre-study visits, and ensuring that investigators and study sites are adequately prepared to conduct the research.
Site Monitoring: CRAs conduct regular site visits to monitor the progress of clinical trials. They verify that the trial is being conducted in accordance with the approved protocol, applicable regulations, and GCP guidelines. This involves reviewing and verifying source documents, ensuring proper documentation and record-keeping, and assessing the adherence to study procedures and regulatory requirements.
Data Collection and Quality Control: CRAs review and validate the accuracy, completeness, and consistency of clinical data collected during the trial. They ensure that data is appropriately entered into electronic data capture (EDC) systems and resolve any data discrepancies or inconsistencies.
Participant Safety and Rights: CRAs are responsible for ensuring the safety and welfare of trial participants. They verify that informed consent procedures are followed, adverse events are reported and managed appropriately, and that participants' rights and well-being are protected throughout the study.
Regulatory Compliance: CRAs work closely with regulatory authorities and ethics committees to ensure that all regulatory submissions, including ethics committee approvals and informed consent forms, are accurate and up to date. They also assist in preparing and reviewing study-related documentation, such as study protocols, case report forms, and study reports.
Collaboration and Communication: CRAs collaborate with various stakeholders involved in clinical trials, including investigators, study coordinators, study sponsors, and contract research organizations (CROs). They provide guidance, support, and training to site staff, and maintain effective communication to address any issues or concerns that arise during the trial.
Overall, the role of a Clinical Research Associate is to ensure the integrity, quality, and compliance of clinical trials, thereby contributing to the generation of reliable and scientifically sound data for the evaluation of new medical treatments or interventions.
Aberdeen (the Granite City) earned its reputation as the "energy capital of Europe "for its significant involvement in the Oil and Gas industry over the last 40 years. Many of the industry key players have a considerable presence in the City and use it as a base for work in the North Sea and beyond. Aberdeen has the largest heliport in the world and an important service ship harbour port serving offshore oil rigs, Aberdeen is often called the "Oil Capital of Europe". The number of jobs created by the energy industry in and around Aberdeen has been estimated at over half a million. The majority of the largest oil fields in the UK sector of the North Sea were found in the waters to the north and east of the Scottish mainland, with the more northerly fields found to the east of the Orkney and Shetland islands. Now, the city is gearing up for the next – and potentially most critical – phase of its evolution, using its proven oil and gas infrastructure and expertise to become a world leader in renewable energy. Significant knowledge and experience in offshore project management, underwater cables and foundations, semi-submersibles, moorings, autonomous vehicles and robotics is transferable and essential to the commercial-scale success of offshore wind and other offshore renewable energy.