Description:The Clinton Health Access Initiative, Inc. (CHAI) was founded in 2002 with a transformational goal: help save the lives of millions of people living with HIV/AIDS in the developing world by dramatically scaling up antiretroviral treatment. When CHAI was founded, many viewed this goal as unreasonable…
The Clinton Health Access Initiative, Inc. (CHAI) was founded in 2002 with a transformational goal: help save the lives of millions of people living with HIV/AIDS in the developing world by dramatically scaling up antiretroviral treatment. When CHAI was founded, many viewed this goal as unreasonable because health systems in poor countries were too weak and prices of relevant drugs and diagnostic tests were too high. CHAI played a leadership role, working alongside governments and other partners, to lower the costs of treatment and help build the in-country systems necessary to provide lifesaving treatment to millions of people. Since then, CHAI has pursued several similarly ambitious goals, from scaling up pediatric AIDS treatment in order to achieve equity with adults in a time frame few thought possible, to rapidly accelerating the rollout of new vaccines.View moreView less
Support the regulatory approval process for Lenacapavir in Indonesia (BPOM/Special Access Scheme) and the development and submission of the IR protocol for ethical review (IRB), under guidance from the Program Manager and regulatory consultants.
Coordinate procurement and distribution of Lenacapavir to approximately 20 study sites across West and East Java, and track related budgets and expenses in line with CHAI's and the donor's financial requirements.
Contribute to the development of the M&E framework with the Ministry of Health, and support routine data extraction from SI PrEP and/or SIHA to track Lenacapavir uptake and continuation.
Support the planning and delivery of training for healthcare workers and civil society organizations on Lenacapavir service delivery ahead of study rollout.
Support implementation research activities across community/private clinics and KP-friendly public health centers in West and East Java, helping ensure data quality for the study's uptake and continuation outcomes.
Coordinate provider surveys and key informant interviews with site staff and study participants.
Support demand generation and community engagement activities tailored to key populations, including MSM/TGW, PWID, and female sex workers, across study sites.
Build and maintain working relationships with the Ministry of Health, BPOM, IRB/ethics committees, study sites, and CSO partners, and represent CHAI at technical working groups and other coordination forums related to HIV and Lenacapavir, as delegated.
Prepare written updates, presentations, and technical materials on the program for internal stakeholders, the Ministry of Health, and, as needed, the donor.
Identify data or process issues affecting program delivery, such as regulatory delays, data quality gaps, or site-level bottlenecks, and recommend practical solutions, escalating issues to the Program Manager as needed.
Interpret and explain program guidance, protocols, and procedures to other team members, field-based consultants, site staff, or CSO partners on specific tasks supporting Lenacapavir implementation research activities.
Contribute to broader CHAI Indonesia country program initiatives and cross-programmatic learning as needed.
Qualifications
Bachelor's degree in Public Health, Medicine, Pharmacy, or a related field; a Master's degree is an advantage.
Minimum of three to five years of relevant professional experience, ideally in HIV/AIDS, public health programs, or implementation/ operations research.
Ability to apply basic project management concepts (planning, execution, monitoring, communication, and closure) with some guidance from a supervisor.
Strong verbal and written communication skills, with the ability to produce clear, well-structured materials with limited oversight.
Ability to identify data or process issues and recommend practical, data-informed solutions.
Experience gathering, reviewing, and validating program or health service data, with high attention to quality and accuracy.
Ability to multitask and manage competing priorities across concurrent workstreams (e.g., regulatory, procurement, training, and M&E) in a fast-paced environment.
Excellent interpersonal skills, including the ability to engage sensitively and without stigma with key populations such as MSM/TGW, PWID, and FSW.
Willingness to travel to study sites in West and East Java.
Advantages
Prior experience with PrEP, long-acting injectables, or other HIV prevention programs.
Familiarity with Indonesia's HIV information systems (SI PrEP and/or SIHA) or experience with health facility data extraction.
Experience supporting regulatory (BPOM) or ethical review (IRB) processes for health products or research studies.
Experience engaging with community-based organizations or key population networks (MSM/TGW, PWID, FSW).
Professional working proficiency in English and Bahasa Indonesia.
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