Employment Type……….Government (permanent) employment basis 

Required No , ……………… 02(two)

Job Grade…………………XIV

Directorate………………. Clinical trial Directorate

Salary……………………9,056.00(ETB nine thousand fifty six)

House Allowance………. Birr 2500 (two thousand five hundred)

Mobile Allowance……….Birr 250(two hundred fifty)

Internet Allowance……… Birr 250(two hundred fifty)

Role and Responsibilities

The Quality assurance /Quality Control officer will be responsible for maintaining QA/QC activities for clinical trial projects. Such activities would include:

• To maintain quality management system for study projects and to develop and to implement monitoring and audit processes, ensuring that all systems are in line with target requirements
• To ensure the trials are conducted, data is generated, documented and reported in compliance with the current approved protocol, good clinical(GCP) and the applicable regulatory requirements.
• Conduct audit/monitoring before the trial, when the trial is ongoing and after the trial is completed or terminated requirements for the quality of the trial related activities have been fulfilled.
• To assist with the preparation for inspections/audits by regulatory authorities
• To ensure that all study participants have written signed consent and/ or assent forms, in the most appropriate language
• Review/audit all trial related documents and prepares monitoring/audit report and follow up.
• Ensure availability, accessibility and adequacy of study supplies and/or equipment incl. IP documentation and accountability.
• To ensur that the trial sites have adequate and up to date essential documentation at all times of the study execution.
• To ensure that all trial related data is accurate, consistent, reliable and has been processed correctly, ready for electronic data capture.
• To ensure that all agreements are in writing with the parties involved in the trial.
•  To follow the institution/CRO established written SOPs as well as those procedures that are specified by the sponsor for monitoring aspecific trial.
• To discuss any major deviations or deficiencies with the investigator(s), Monitor(s) and Research supervisor(s) for corrective and preventive action.
• Conduct clinical trial system audit

Job Requirements

• BSc Degree in Pharmacy, Public health, nursing with demonstrated experience 2 years related experience.

How to Apply

Interested applicants who fulfilled the above requirements should  send the following through ethiojobs.net with in ten /10/working days since the vacancy posting.

Ø A CV/resume (not more than 6 pages)

Ø  A cover letter (not more than one page)

Ø A one /two pages table summarizing your educational background, technical skills and competencies to facilitate the screening process.

         Female applicants are encouraged