Summary
Date Posted: Wednesday, September 29, 2021 , Base Salary: Not Disclosed

JOB DETAILS:

Africa Medical and Behavioral Sciences Organization (AMBSO) www.ambso.org is a ‘Private Not for profit (PNFP) organization working in partnership with Uro Care Hospital, with its Head offices at Nansana, along Hoima Road and satellite offices in Hoima and Masaka. AMBSO conducts a wide range of activities of public health interest including clinical research, community-based health surveillance research; programs for health care service delivery and capacity building among health care workers and community health workers.
With funding from Gilead Sciences Inc. and in collaboration with MUJHU care limited, AMBSO will participate in a six year multi-site PURPOSE 1 study that is aimed at evaluating the efficacy of Lenacapavir (LEN) and Emitricitabine/Tenofovir Alafenamide (F/TAF) in preventing HIV transmission among adolescent girls and young women (AGYWs) at high risk of acquiring HIV infection. AMBSO is seeking for qualified, committed and reliable professionals to work at its Masaka and Hoima research sites. Applications are therefore invited from interested persons to fill the position listed above.

Location: Hoima and Masaka sites
Reporting to: Study Principal Investigator

Key Duties and Responsibilities:
• To conduct real time evaluation and verification that all requirements for the quality of the trial related activities have been fulfilled.
• To ensure that data is generated, documented and reported in compliance with the current approved protocol, Good Clinical Practice (GCP) and the applicable regulatory requirements.
• To ensure that all study participants have written signed informed consent forms before enrolment into the study.
• Support regulatory supervision and other monitoring visits by giving guided access to requested data.
• Assist Study Coordinators in compilation and submission of the regulatory documents to the relevant Regulatory Authorities.
• To ensure that all trial related data is accurate, consistent, and reliable and has been processed correctly, ready for electronic data capture.
• Participate in staff training and retraining.
• To discuss and participate in documentation of major deviations or violations with the Investigators and research supervisors for corrective and preventive actions.
• Any other duties as assigned from time to time.

Essential Qualifications/ requirements:
• A registered health professional e.g Medical Officer, Pharmaceutical Scientist, Nurse or
Midwife, Clinical Officer or related Qualification with at least 3 years working experience in
a busy Research Institution setting.
• Prior experience with clinical trials or Implementation Science Research is desirable.
• Evidence of training in Good Clinical Practice (GCP) and Human Subject Protection (HSP).
• The applicant should be computer literate especially with Microsoft Computer packages.
• Excellent communication, organizational and interpersonal skills
• The ideal candidate must be someone who pays attention to detail, able to multi-task and
willing to work longer hours.

Work Hours: 8

Experience in Months: 36

Level of Education: Professional Certificate

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Job application procedure

Qualified and interested applicants should submit their application letter, valid academic documents and detailed resume (CV) with three recognizable referees to: Uro Care-AMBSO office-Nansana (Behind Bukomero Seven sisters building, Nakuule Zone). Emails: info@ambso.org. (PDF file only).

Applications should be handed in not later than 5:00pm 15th October, 2021. NB: Please clearly
indicate the Research site that you are applying for (either Masaka or Hoima)

Only shortlisted candidates will be contacted.

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