Committed clinical research professional. Demonstrated ability to support management and coordinate the tasks of multiple clinical research studies. Possess excellent communication skills and the ability to present results in a clear and actionable format for investigators, sponsors, regulatory bodies, or other consulting professionals.Clinical Trial Management with a demonstrated history of working in the research industry.I have experience in Pre-study activities, (Feasibility, Site Selection Visit), Study Start-Up, EC submission, Essential Document generations on a priority basis, Subject recruitment and retention, Ensuring proper documentation in the Source Document in real-time, accountability and distribution of IP, Site / Sponsor’s relations, EC communication, regulatory requirements. Audit preparation activities and Good knowledge of ICH-GCPAdhere to research SOPs, GCP & Protocol to ensure the integrity of data & protection of rights, safety & well-being of enrolled subjects in clinical trials.Areas of expertise – Oncology, Ophthalmology, Pulmonology, Orthopedics, COVID-19, Rare Diseases.looking forward to working & coordinate with a strong team in clinical research wherein, I can learn & develop my professional experience & put up my maximum effort to make the work done perfectly by using all my skills from my previous experience.