Clinical Research Professional
5 days ago
At IQVIA, we seek a skilled Clinical Research Associate to ensure that sites are conducting studies and reporting data as required by the study protocol, applicable regulations, and sponsor requirements.
This role involves performing site monitoring visits, working with sites to adapt subject recruitment plans, administering protocol training, and evaluating the quality of study site practices.
You will manage the progress of assigned studies by tracking regulatory submissions, recruitment and enrollment, case report form completion, and data query generation and resolution.
Key Responsibilities- Perform site monitoring visits in accordance with contracted scope of work and regulatory requirements.
- Work with sites to adapt subject recruitment plans and track their progress.
- Administer protocol training to assigned sites and establish regular lines of communication.
- Evaluate the quality of study site practices and escalate quality issues as necessary.
- Manage the progress of assigned studies by tracking various metrics.
- Bachelor's Degree in a scientific discipline or healthcare preferred.
- At least 1 year of on-site monitoring experience.
- Good knowledge of clinical research regulatory requirements and therapeutic knowledge.
- Excellent communication and organizational skills.
- Ability to establish and maintain effective working relationships.
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Clinical Research Associate
5 days ago
Kwai Tsing District, Hong Kong SAR China IQVIA Argentina Full timeJob DescriptionThe Clinical Research Associate will be responsible for monitoring and managing research sites to ensure compliance with study protocols, regulations, and sponsor requirements.Key responsibilities include:Performing site monitoring visits to verify adherence to protocol and regulatory requirements;Working with sites to develop and track...
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Clinical Research Associate
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kwai tsing district, Hong Kong SAR China IQVIA Argentina Full timeJob OverviewIn this role as a Clinical Research Associate, you will be responsible for ensuring the proper conduct of clinical studies at assigned sites. Your primary goal will be to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations, and sponsor requirements.
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Clinical Research Associate
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kwai tsing district, Hong Kong SAR China IQVIA Argentina Full timeJob Overview Perform 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 and guidelines, and sponsor requirements. Essential Functions Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with...
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Clinical Research Associate
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Kwai Tsing District, Hong Kong SAR China IQVIA Argentina Full timeJob OverviewPerform 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 and guidelines, and sponsor requirements.Essential FunctionsPerform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with...
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Research Site Manager
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kwai tsing district, Hong Kong SAR China IQVIA Argentina Full timeAbout the RoleWe are seeking a highly skilled Clinical Research Associate to join our team at IQVIA Argentina. In this role, you will be responsible for ensuring the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.You will work closely with sites to monitor their progress,...
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Kwai Tsing District, Hong Kong SAR China IQVIA Argentina Full timeJob OverviewThis position involves overseeing the conduct of clinical research studies at various sites, ensuring that they are performed in accordance with established protocols, regulations, and sponsor requirements.Main duties include:Conducting regular site visits to monitor compliance with study protocols and regulatory requirements;Developing and...
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