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Job description :
Job Responsibilities:
• Oversee the progress of a Clinical Trial, ensuring that it is conducted, recorded and reported in accordance with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP) and the applicable Regulatory requirements
• Administer protocol and related study training to assigned site
• Establish regular lines of communication with sites to manage ongoing project expectations and issues
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Qualifications :
Requirements:
• Degree in Science, with a major in Pharmacy, Biological / Life Sciences or Nursing from a recognized tertiary institution
• A minimum of 3 years clinical monitoring experience, pharmaceutical / CRO industry is a must
• Good knowledge of drug development process, clinical trial monitoring procedures, medical terminology and GCP/ICH guidelines
• Excellent organizational and problem solving skills
• Strong written and verbal communication skills
• Willing to travel when required
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