ALIMA Is Hiring a Clinical Research Referent for the EBO-PEP Project: 12-Month Opportunity | Apply by 24 November 2026

Overview

ALIMA is seeking an experienced Clinical Research Referent to support the EBO-PEP project, which is a clinical trial investigating post-exposure prophylaxis against the Bundibugyo Ebola virus disease in the Democratic Republic of Congo. The initial duration of the position is 12 months with an immediate start, and the role involves working under the supervision of the Emerging Infectious Diseases research unit coordinator. The location and engagement arrangements are determined based on the selected candidate's profile and potential collaboration with research partner institutions, and the role may involve occasional travel to research sites in the Democratic Republic of Congo.

Who can apply

Applicants must hold higher education qualifications in medicine, pharmacy, paramedical or biomedical sciences, public health, epidemiology, or an equivalent discipline, accompanied by additional scientific or research training. Candidates need confirmed experience in clinical research, specifically in clinical trial methodology and research protocol development, along with experience working with investigators, scientific teams, or research institutions. Individuals must possess an understanding of ethical, regulatory, and methodological requirements for clinical trials, and professional fluency in both written and spoken French and English. Previous experience in infectious diseases, epidemic research, or humanitarian operations serves as an advantage.

What you get

The position offers a 12-month contract with a salary based on ALIMA's salary scale. ALIMA may recruit the successful candidate directly or through an arrangement with a research institution, such as secondment or temporary placement.

Requirements

Candidates are required to coordinate the drafting, review, and updating of the EBO-PEP research protocol, including defining research objectives, methodologies, study procedures, and scientific evaluation methods. The role requires preparing and reviewing scientific documents, coordinating submissions to ethics committees and regulatory authorities, and ensuring compliance with Good Clinical Practice requirements and ICH E6 R3 standards. Additional duties include working with monitoring and data management teams, maintaining working relationships with consortium partners, organizing scientific discussions, monitoring project timelines, supporting research communications and publications, and assisting operational teams with study implementation in the Democratic Republic of Congo.

How to apply

Interested candidates must submit a complete application online before the deadline, consisting of an updated curriculum vitae in PDF format and a motivation letter. Applications are reviewed in the order they are received, and the organization may close the vacancy prior to the deadline if a suitable candidate is found. Female candidates are strongly encouraged to apply.

Key dates

The application deadline is 24 November 2026. The position offers an immediate start as soon as possible.