A multinational company located in Nasr City is looking for Experienced Clinical Research Associate (Full-time).

Qualification : Bachelor of Pharmaceutical.

Experience : Minimum 2 years of experience as a Clinical Research Monitor.

Skills : Knowledge of GCP principles, Clinical studies procedures and guidelines.

Responsibilities:

• Ensure the delivery of Phase II or Phase III clinical trial within the time frame, and are conducted in accordance with G.C.P and applicable ethical and regulatory requirements, SOPs and project Gantt chart.

• Act as the main line of communication with the principal investigators and his/her team and the CRO.

• Follow up the procedures for manufacturing, dispensing, and return of investigational product(s) and ensure that they are safe, adequate and properly documented in accordance with local regulations and the trial protocol

Job Requirements: Knowledge of GCP principles, Clinical studies procedures and guidelines.

If you are interested , please send your CV to [email protected]

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