Gain real-world skills through online learning and expert-led sessions, preparing you for a successful career in Clinical Research and Medical Coding.
This training enhances their ability to use pharmacovigilance tools and methodologies, crucial for maintaining compliance with regulatory standards and improving overall healthcare outcomes.
Enhance your skills, gain certification, and advance your career in clinical research. Enroll now for in-depth training and real-world applications.
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Coordinates clinical trial activities at research sites, ensuring protocol compliance and patient safety. Acts as a bridge between investigators, sponsors, and ethics committees.
Handles collection, cleaning, and validation of clinical trial data. Works with EDC tools to ensure data accuracy and regulatory compliance.
Processes and evaluates adverse drug reaction reports (ICSRs). Ensures timely reporting to regulatory authorities using PV tools.
Creates clinical trial documents like protocols, reports, and summaries. Requires medical knowledge, strong writing skills, and familiarity with ICH-GCP.
Assists in preparing and submitting regulatory documents for product approvals. Monitors global regulatory guidelines and supports compliance.
Documents real-time patient-physician interactions into electronic medical records. Improves doctor efficiency and accuracy in clinical documentation.
At Cliniversity, we pride ourselves on our outstanding placement record in the clinical research sector. Our students are highly sought after by top CROs and leading research institutions. With a robust training program and hands-on experience, our students are well-equipped to excel in roles such as Clinical Research Associates, Data Managers, and Pharmacovigilance Specialists. Join us and launch your career with confidence, knowing you have the skills and support to succeed in the dynamic field of clinical research!
