Follow and comply with the Company’s established procedures and policies.
Follow and comply with the Company’s QMS, ISMS and PIMS requirements.
Responsible for confidentiality, integrity, availability and safeguarding of data.
Responsible for reporting of security incidents and PIMS breaches as applicable.
CRF/DCF tracking.
Develop test scripts and execution logs for User Acceptance Testing (UAT).

🎯 Requirements

Bachelor’s degree in clinical/pharmacy/biological/mathematical sciences or nursing (2 yrs clinical exp).
Working knowledge of GCP, clinical research, and regulatory terminology.
Solid understanding of clinical drug development process.
Detail-oriented.
Strong communication and team coordination.
Training on QMS/ISMS/PIMS requirements.

🎁 Benefits

Flexible Working Hours
Team events and end of year party
Employee satisfaction survey for feedback
Health Insurance

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