ALMA PRESENTATION
THE ALIMA SPIRIT : ALIMA’s reason for being is to save lives and provide care to the most vulnerable populations
vulnerable people, without any discrimination based on identity, religion or politics, through actions
based on proximity, innovation, and alliances between organizations and individuals. We act with
Humanism, impartiality, and respect for universal medical ethics. To access the
To our patients, we are committed to intervening in a neutral and independent manner.
The values and principles guiding our actions, as outlined in our Charter :
1. The patient first
2. Revolutionizing humanitarian medicine
3. Responsibility and freedom
4. Improve the quality of our actions
5. Trust
6. L’intelligence collective
7. Environmental Responsibility
ALIMA promotes and defends fundamental human rights principles. ALIMA has an approach to
zero tolerance towards those guilty of acts of sexist and sexual violence
than inaction in the face of alleged or proven acts of violence. The protection of people
benefiting from and impacted by our intervention is our absolute priority in everything we do.
Let’s do this. Everyone collaborating with ALIMA agrees to:
● Respect the charter, the code of conduct, and institutional policies, including the policy
protection against abuse of power and gender-based and sexual violence, the policy of
prevention of corruption and fraud;
● Report any violation of policies, framework documents and procedures to a superior, a
superior, a contact person, or at alert@alima.ngo
HEAL – INNOVATE – TOGETHER:
Since its creation in 2009, ALIMA has treated more than 10 million patients, and is deploying
Today, its operations are in 14 African countries. By 2026, we had developed 54 projects.
humanitarian medical response to meet the needs of populations affected by conflict,
epidemics and extreme poverty. All of these projects are carried out in support of the authorities
national health systems through primary healthcare provided in the community and in the
health centers as well as secondary and tertiary care. We work in partnership,
particularly with local NGOs, whenever possible, to ensure that our patients and
Patients benefit from expertise wherever it is found, whether at the level of their country or elsewhere
of the world. Furthermore, to improve the humanitarian response, we are conducting projects to
operational and clinical research, particularly in the field of combating
Malnutrition, pediatrics, maternal health, and viral hemorrhagic fevers. ALIMA leads
also several responses to epidemic emergencies such as Ebola, Lassa fever, the
cholera, Mpox, diphtheria, meningitis, measles, etc.
OUR PROJECT THEMES : Malnutrition, Sexual and Reproductive Health including violence
based on gender, primary and secondary health, pediatrics, epidemics, surgery, mental health and
research.
OUR COUNTRIES OF OPERATION : Mali, Burkina Faso, Central African Republic, Nigeria, Niger, Chad,
Democratic Republic of Congo, Cameroon, Guinea, South Sudan, Mauritania, Ethiopia, Haiti
and Sudan.
Job context
Research at ALIMA: the Emerging Infectious Diseases (EID) unit
ALIMA’s Emerging Infectious Diseases (EID) research unit designs and coordinates
clinical research projects in Africa, particularly on viral hemorrhagic fevers (Ebola,
Lassa) and other diseases with epidemic potential.
At the interface between scientific research and humanitarian action, the center works in partnership
with scientific institutions, investigators, study sponsors and teams
ALIMA’s operational activities in order to develop and implement clinical research projects
adapted to epidemic contexts.
In this context, ALIMA notably coordinates the EBO-PEP consortium, dedicated to a clinical trial
concerning post-exposure prophylaxis against Ebola Bundibugyo virus disease in the Republic
Democratic Republic of Congo.
Implementing this trial requires solid scientific and methodological expertise.
particularly for the drafting and adaptation of research protocols, the production of the
scientific and regulatory documentation and coordination with the various partners of
the study.
To strengthen this scientific dimension, ALIMA is looking for an experienced professional.
in clinical research, capable of contributing directly to the organization of the consortium, the
production of EBO-PEP trial documents and working closely with investigators and
partner research institutions.
The position is situated within an environment combining scientific expertise and clinical research in
Humanitarian context. ALIMA’s specific operational skills for interventions
will be developed gradually, in collaboration with the MIE cluster teams and the
field teams.
Main mission
Under the responsibility of the MIE unit coordinator and in close collaboration with the
principal investigators, sponsors and partners of the EBO-PEP consortium, the or the
The Clinical Research Lead is responsible for coordinating the consortium, from scientific design and
methodological aspects of the trial, as well as the development of the documents necessary for its implementation, in
ensuring compliance with regulatory requirements and quality standards applicable to the
clinical research.
Main activities
1. Ensure the drafting and scientific monitoring of the EBO-PEP study protocols
● Coordinate the drafting and updating of the EBO-PEP research protocol, based on
scientific guidelines defined by the investigators and partners of the study.
● Contribute to the formalization of objectives, methodologies, study procedures and
methods of scientific evaluation.
● Ensure the scientific and methodological consistency of the different components of the
protocol.
● Coordinate the contributions of investigators, the sponsor, and scientific experts to
the drafting of the study documents.
● Prepare and monitor amendments to the protocol, particularly in light of developments
scientific, regulatory and constraints encountered during implementation.
● Conduct the necessary bibliographic research and scientific syntheses for the
preparation and development of research documents.
2. Coordinate the scientific and regulatory documentation for the trial
● Contribute to the development and revision of scientific documents necessary for the
conduct of the EBO-PEP test.
● Participate in the preparation of submission files for ethics committees and authorities
competent regulatory bodies, in collaboration with the promoter and partners
concerned.
● Ensure that documents and procedures comply with Good Clinical Practice (ICH)
E6 R3) and applicable regulatory requirements.
● Collaborate with the monitoring and data management teams in the development and
consistency of study documents, including source documents and Case Reports
Forms (CRF) and associated procedures.
● Ensure the tracking of versions, revisions and validation of scientific documents and
regulatory matters within its scope.
● Contribute to the scientific and documentary preparation of audits and reviews of
compliance.
3. Participate in the coordination of the EBO-PEP consortium
● Maintain close working relationships with investigators, the sponsor, the
scientific institutions and other consortium partners.
● Organize and facilitate the scientific exchanges necessary for the preparation, development and
to follow up on the study.
● Prepare and contribute to the facilitation of meetings, working groups and committees of the
consortium.
● Ensure adherence to the commitment schedule and the production of expected deliverables
to the funding agency.
● Contribute to the preparation of scientific reports and documents intended for
partners and landlords.
● Participate in the scientific dissemination of research, particularly through the preparation of
communications, reports and publications, in collaboration with the investigators.
4. Contribute to the operational implementation of the EBO-PEP study
● Work with ALIMA’s operational teams and field partners to facilitate
the translation of protocols and procedures into research activities.
● Provide scientific and methodological support during the preparation, launch and
monitoring of trial activities in the DRC.
● Contribute to identifying difficulties that may affect the proper implementation of the
protocol and propose the necessary adaptations, in consultation with the parties
stakeholders.
● Participate in the preparation and scientific and methodological training of the teams
search on implementation sites.
● When necessary, travel to research sites to
to support the teams and contribute to the scientific monitoring of the study.
Experiences and skills
Education
● Higher education in medicine, pharmacy, paramedical and biomedical sciences,
public health, epidemiology or equivalent discipline.
● Additional training or a scientific research background is required.
Professional Experience
● Proven experience in clinical research, particularly in methodological design
and the drafting of study or clinical trial protocols.
● Experience collaborating with investigators, scientific teams, or
research institutions.
● Sound knowledge of the ethical, regulatory, and methodological requirements applicable
to clinical trials.
● Experience in infectious diseases or research in an epidemic context
would be an asset.
● Prior experience in a humanitarian environment or in operational
field coordination is an advantage, but not essential.
Required Skills and Qualities
● Excellent scientific writing skills.
● Strong command of clinical trial methodology and Good Clinical Practice (GCP).
● Ability to analyze, structure, and synthesize complex scientific information.
● Ability to work collaboratively with scientific teams and
institutional partners.
● Methodological rigor, autonomy, organizational skills, and ability to work in a
multidisciplinary environment.
● Interest in clinical research applied to public health issues in
humanitarian contexts.
● Professional proficiency in written and spoken French and English.
Location and methods of collaboration
Location and terms of employment to be defined according to the selected profile and the possibilities for
collaboration with partner research organizations.
The position may be filled through direct recruitment by ALIMA or through collaboration
with a research institution, particularly in the form of a secondment or temporary assignment,
according to the agreed terms.
Occasional travel to research sites, particularly in the Democratic Republic of
Congo, may be necessary.
- Contract duration: 12 months
- Start date: As soon as possible
- Salary: According to ALIMA salary scale
How to apply
- To apply, please submit your CV and cover letter online before December 4, 2026 here.
- Applications are processed in the order they are received.
- ALIMA reserves the right to close the offer before the initially indicated deadline if a candidate is successful.
- Only complete applications (CV in PDF format + Cover Letter) will be considered.
- Applications from women are strongly encouraged.