Clinical Research Associate

Job description

About the Role The Clinical Research Associate (CRA) is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, complete, and verifiable from the source documents. The CRA is the primary contact between the Investigational Sites, Novotech, and Sponsor. Key responsibility of a CRA is as a site relationship manager ensuring that clinical trials are conducted in accordance with ICH GCP guidelines, local and global regulatory requirements, and Novotech/Client SOPs. Experience and Qualifications: - Graduate in a clinical or life sciences-related field. Relevant experience/qualifications in allied professions may also be considered. - Must have good time management skills, attention to detail, be able to work well in a team, and be computer literate. - Preferably experience of working in the research, pharmaceutical industry or a related field per job level as follows: - At least 2-3 years of Clinical Research Associate experience in the Clinical industry. - Excellent interpersonal and team skills with a genuine commitment to contributing to the development of innovative treatments Responsibilities: Novotec...