Clinical research professional with 4 years of experience in clinical research. Knowledge of Canadian Food and Drug Regulations, strong understanding of ICH-GCP, clinical trials, regulatory requirements and applicableSOPs. Also familiar ICH-GCP guidelines from conducting Phase I to IV trials and clearly understands the responsibilities of a clinical research and regulatory affairs professional.
Highly motivated, excellent communication and interpersonal skills while working as an effective team member.
Seeking an opportunity to transfer and demonstrate my skills in Clinical research and regulatory affairs to ensure that drug development processes and clinical trials are conducted in accordance with the applicable local and federal regulatory requirements.