Job DescriptionJob Title: Clinical Research Associate (CRA)/ Senior Clinical Research Coordinator
nCompany: MS Clinical Research Pvt Ltd
nExperience: Minimum 3 years
nAbout Us
nMS Clinical Research (MSCR) is a leading clinical research organization committed to advancing scientific innovation and improving healthcare outcomes. We conduct high-quality clinical trials that adhere to global standards of excellence and contribute to the development of breakthrough medical solutions.
nJob Summary
nWe are seeking an experienced and proactive Clinical Research Associate (CRA/ Sr. CRC) with a minimum of 5 years of relevant experience in clinical trial monitoring and site management. The CRA will be responsible for overseeing the conduct of clinical trials, ensuring regulatory compliance, maintaining data integrity, and mentoring junior CRAs and CRCs. This role requires exceptional organizational, analytical, and communication skills, along with the ability to build robust site relationships and ensure study success.
nKey Responsibilities
nSite Management & Oversight
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Conduct and oversee site initiation, interim monitoring, and close-out visits in accordance with study protocols, GCP, and applicable regulatory guidelines.n
Build and maintain robust qualified relationships with investigators, site coordinators, and key stakeholders.n
Proactively identify and resolve site issues to ensure quality and compliance.n

nClinical Trial Monitoring
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Perform comprehensive monitoring visits to assess site performance, data accuracy, and adherence to protocol.n
Ensure timely follow-up on monitoring findings, query resolution, and documentation in compliance with SOPs.n
Support risk-based monitoring activities and provide oversight to ensure data reliability.n

nProtocol & Regulatory Compliance
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Ensure that all trial activities comply with study protocols, SOPs, and local/international regulations.n
Participate in the preparation an

📌 Senior Clinical Research Associate Vasanthanagar
🏢 MS CLINICAL RESEARCH
📍 Vasanthanagar