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Job description :
Job Responsibilities:
* Oversees 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
* Minimum 1 year of clinical monitoring experience in the pharmaceutical / CRO industry.
* For Senior Research Associate position, minimum 3 years clinical monitoring experience, preferably with some experience in leading clinical teams in the region
* 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
* Ability to travel when required
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