Clinical Research Associate I IQVIA India

1.0 - 5.0 years

0 Lacs

delhi

On-site

As a Clinical Research Associate -I, your role will involve performing monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations, guidelines, and sponsor requirements. Your essential functions will include conducting site monitoring visits, working with sites to drive subject recruitment plans, administering protocol and study training to sites, and evaluating the quality and integrity of study site practices. You will also be responsible for managing the progress of assigned studies, maintaining documentation regarding site management, collaborating with study team members, and supporting the development of project subject recruitment plans. To qualify for this position, you must have a degree in BPharm, MPharm, BDS, BAMS, or BHMS. Additionally, you should have at least 1-2 years of on-site monitoring experience and a good knowledge of applicable clinical research regulatory requirements such as Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Furthermore, you should possess good therapeutic and protocol knowledge, computer skills including proficiency in Microsoft Word, Excel, and PowerPoint, as well as written and verbal communication skills. Organizational, problem-solving, time management, and financial management skills are also important for this role. Lastly, you should be able to establish and maintain effective working relationships with coworkers, managers, and clients.,

Posted 2 days ago

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