Key Responsibilities:


Ensure adherence to ICH-GCP, local regulations, and ethical standards.
Monitor compliance with study protocols, SOPs, and sponsor requirements.
Identify deviations, non-compliances, or risks, and ensure CAPA (Corrective and Preventive Actions) are implemented.
Support inspection readiness for audits by regulatory authorities and sponsor.
Train clinical trial staff on GCP, SOPs, and QA best practices.
Provide ongoing QA guidance and support to research teams.
Identify and escalate quality issues or trends affecting trial integrity.
Develop and implement quality improvement initiatives based on audit findings and process reviews.
Assisting in preparing the project for monitoring of quality assurance Activities;
Assisting in carrying out internal audits on quality compliance and follow-up audits;
Oversee daily quality checks and error resolution


Vacancy Requirements:


Bachelor’s Degree in Biomedical Sciences, Nursing, Health sciences or any other relevant field from a recognized Institution;    Mandatory
Proficient in computer applications;    Mandatory
One year of relevant experience in clinical research, or quality management.    Mandatory
Planning skills;    Mandatory
Creativity and innovation skills;    Mandatory
Analytical skills;    Mandatory
Communication and reporting skills;    Mandatory
Interpersonal skills;    Mandatory
Ability to work independently and Team player.    Mandatory