Ideal Candidate Profile:
➢ A minimum of 2+ years clinical trials experience as study-coordinator, with a good knowledge of ICH/GCP guidelines
➢ ICH/GCP valid training
➢ Good knowledge of English language
➢ Team player with strong presentation and leadership skills
We are looking for a person with a high level of professionalism, complex personality, with vision and persuasion, a person who, through hard work and dedication to the profession, can lead to the promotion of high quality health services.
➢ Supporting the Principal Investigator and Subinvestigators’ team with clinical studies activities
➢ Liaise with CRAs to ensure the performance of clinical studies ; ensure quality standards; resolve logistic and practical issues clinical trial related and promote the team-working environment
➢ Develop a good knowledge of the study protocol and other relevant documentation
➢ Interact with CCBR Clinic staff regarding objectives and status of clinical projects
➢ Ensure regulatory compliance with ICH/GCP guidelines, and company SOP's
• motivating salary package
• training and development programs
• stimulating professional environment
Part of a multinational company with an experience of over 10 years in healthcare and medical
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