B.Sc Lifescience Job as Clinical Research Associate at MS Clinical Research – Apply Now!
Are you a Lifescience graduate with clinical trial experience? MS Clinical Research Pvt Ltd is hiring a Clinical Research Associate (CRA) with 3+ years of experience to support high-quality clinical trials. Join a dynamic team dedicated to improving healthcare outcomes through regulatory-compliant research and innovation. Apply now to advance your career in clinical research!
About MS Clinical Research Pvt Ltd
MS Clinical Research (MSCR) is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. We are committed to conducting high-quality clinical trials and contributing to the development of innovative medical solutions.
Job Title: Clinical Research Associate (CRA)
Job Summary:
We are seeking a highly motivated and experienced Clinical Research Associate (CRA) with a minimum of 2-3 years of relevant experience…
Key Responsibilities:
Site Management:
Conduct site initiation, routine monitoring, and close-out visits to ensure compliance with the study protocol, Good Clinical Practice (GCP), and regulatory requirements. Build and maintain strong relationships with investigative sites, investigators, and study coordinators.
Clinical Trial Monitoring:
Perform routine monitoring visits to assess site performance, data integrity, and regulatory compliance. Ensure timely resolution of data queries and issues
identified during monitoring visits.Protocol Compliance:
Ensure that all study activities are conducted in accordance with the approved protocol, SOPs, and applicable regulatory guidelines. Collaborate with investigators to address and resolve protocol-related queries.
Regulatory Compliance:
Assist in the preparation and submission of regulatory documents to ethics committees and regulatory authorities. Stay informed about changes in regulatory requirements and update study teams accordingly.
Data Management:
Collaborate with data management teams to ensure accurate and timely data collection and entry.
Perform source data verification and data validation activities.
Safety Reporting:
Monitor and report adverse events in compliance with regulatory requirements and safety reporting procedures. Ensure that safety reports are submitted to relevant authorities and stakeholders.
Training and Support:
Provide training and support to site staff on study protocols, data collection, and regulatory compliance. Act as a resource for investigators and site staff throughout the duration of the study.
Requirements:
- Education: Bachelor’s degree in a relevant Lifescience field.
- Experience: Minimum of 3 years as a Clinical Research Associate.
- Regulatory Knowledge, Communication Skills, Organizational Skills, Team Collaboration, Travel.
Benefits:
- Competitive salary and benefits package.
- Opportunities for professional development and advancement.
- Collaborative and dynamic work environment.
Join our team at MS Clinical Research and contribute to the advancement of clinical research and the development of innovative healthcare solutions.
Keywords: Clinical Research Associate, CRA, Clinical Trials, Healthcare, Regulatory Compliance, Data Management, B.Sc Lifescience Job, Lifescience
