Conducts Site Selection for potential sites to evaluate their capabilities for conducting a clinical trial
Performs SiteInitiation Visits and ensures site personnel is fully trained on all trial-related aspects.
Implements site management activities to ensure compliance with protocol, GCP, local regulations, and local processes to secure data integrity and patient safety.
Monitors studies as per current legislations, ICH/GCP, and Sponsor(s) standards.
Performs Site Closeout activities per SOPs and applicable regulations to ensure that the site is aware of any follow-up activity and archiving requirements.

• Bachelor's degree in Life Sciences or Health Care
• Good knowledge of international guidelines ICH-GCP as well as relevant local regulations.
• Good knowledge of the drug development process specifically clinical trial/research
• Great planning and organizational skills
• Good communication skills, and ability to influence others.
• Good strategic thinking: Ability to anticipate potential issues and take appropriate actions with or without supervision.
• Fluent in both written and spoken English.
• Having experience in Clinical Trials at least 2 years will be considered favourably.

• Accommodation allowance (in other provinces)
• Fuel/transportation fees
• Telephone bill allowance
• Work from home
• Social security
• Health insurance
• Flexible working hours
• Ordination leave
• Annual trip or party
• Annual bonus