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RA Executive FDF Dossiers Ultratech India

5.0 - 10.0 years

5 - 9 Lacs

mumbai

Work from Office

Manage and maintain accurate records of clinical trial data. Coordinate with cross-functional teams to ensure timely completion of studies. Develop and implement effective study protocols and case report forms. Conduct site visits to monitor progress and ensure compliance with regulations. Collaborate with stakeholders to resolve issues and improve processes. Ensure data quality and integrity through regular audits and reviews. Job Requirements Strong knowledge of Good Clinical Practice (GCP) and regulatory requirements. Experience with electronic data capture systems and software applications. Excellent communication and interpersonal skills. Ability to work independently and as part of a t...

Posted 1 day ago

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