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Health Associate Researcher (Study Physician)

Armauer Hansen Research Institute

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Health Care

Public Health

Addis Ababa

Position

2021-10-20

to

2021-11-01

Required Skills
Required skills have not yet been specified for this position this job
Fields of study
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Full Time

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Job Description

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

Required No , ……………… 01(one)

Job Grade…………………XVI

Directorate………………. Clinical trial Directorate

Salery……………………11,305.00(ETB eleven thousand three hundred five)

House Allowance………. Birr 6000 (six thousand)

Mobile Allowance……….Birr 500(five hundred)

Internet Allowance………Birr 500 ( five hundred fifty)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 ensure 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, and 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 specific 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 and 4 publications points.

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

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