Clinical Trial Management: Oversee the planning, implementation, and execution of clinical trials in compliance with regulatory guidelines, good clinical practices (GCP), and study protocols.
Project Planning: Develop detailed project plans, timelines, and budgets for clinical research studies.
Regulatory Compliance: Ensure that all clinical research activities adhere to applicable regulatory requirements and ethical standards.
Site Selection and Management: Identify and select clinical trial sites, manage site relationships, and ensure smooth site operations.
Participant Recruitment: Develop strategies for participant recruitment and retention to meet enrollment goals for clinical trials.
Data Management: Ensure accurate and timely collection, analysis, and reporting of clinical trial data.
Safety Monitoring: Implement safety monitoring protocols to ensure the well-being of trial participants.
Collaboration with Investigators: Work closely with principal investigators and medical professionals involved in the research studies.
Vendor Management: Collaborate with external vendors, such as contract research organizations (CROs), to support clinical trial activities.

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5 -10 Years in Clinical Research (Mainly in Ethics Committee)
MSc Clinical Research/ Life Science

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Manager – Clinical Research