- We are looking for a colleague who will provide operational excellence, a business mind-set and will help develop new ways of value addition to our patient-centric programs and solutions. Self-motivation, problem solving, team oriented and a positive work attitude should be your core capabilities, in return we offer a position in an organization that works at the forefront of healthcare innovation.
Key Responsibilities
Clinical guidance
- Responsible for delivering clear, documented content, medical analysis and advice, specifically to product/program development, decision making and implementation.
- Provide deep knowledge of active/planned programs, experiments or pilots on products, or solutions that the organisation may pursue.
- Contribute medical context into marketing and commercial strategies aimed at developing market driven solutions for sustainability of targeted programs, services or products
- Translate complex medical information, guideline and regulatory provisions into understandable content and context for various programs, products or audiences.
Medical research and Innovations:
- Serve as a medical counterpart to external researchers evaluating PharmAccess’ interventions in Kenya, as local research coordinator, in collaboration with PharmAccess Research & Learning Amsterdam
- Contribute to setting up, and implementing medical interventions as part of PharmAccess patient care journeys in Kenya
- Provide technical support to the Kenya PharmAccess epidemic preparedness strategy, including (private sector) IDSR monitoring, predictive modeling in line with the new Kenyan National Health Security agenda
- Secure (third-party research on) PharmAccess interventions to be in line with national ethical standards (clearance) and NACOSTI compliance
- Co-analyze and critically assess quality of clinical data, perform interim analyses, in collaboration with Amsterdam PharmAccess R&L team
- Secure medical correctness of PharmAccess’ projects information dissemination and communications in Kenya
- Identify and follow up on funding opportunities for clinical research in collaboration with PharmAccess R&L Team Amsterdam
Program Development:
- Responsible for ensuring PharmAccess programs and research work meet standards required by medical and regulatory agencies.
- Coordinate programs and provide clinical documented content and advice as needed to ensure programs achieve set goals
- Responsible for design and review of medical Key Performance Indicators linking to our different programs
- Work closely together with our Kisumu site/UHC teams, identify supply side gaps, develop measurable health outcomes, and provide advice on the benefit package.
- Support the development of medical content for M-TIBA packages (MomCare, Safe Mama-Tech, Insurance packages and any other new or existing value-based [VBHC] initiatives).
- Contribute to development of clear, cross-cutting measurable health outcomes and identify new opportunities for improvement or addition to digital packages that benefit the clients.
- Provide input to the medical content of SafeCare in alignment with SafeCare’s strategic direction, and in agreement with the SafeCare leadership to further strengthen the SafeCare monitoring.
- Ensure that standards are in tandem with local context, policy and regulatory provisions
- Provide regular training to PST and SafeCare team in conjunction with experts
- Conduct a final evaluation to determine project outcomes, key learnings and implications
- Support the advocacy and dissemination of program learnings to integrate into practice and policy for the benefit of healthcare consumers
Key stakeholder engagement
- Build and retain relations with the relevant parties including Key Opinion Leaders and academic centres within the public and private sector and attain influential understanding and input in decision making
- Deliver scientific presentations and capacity building to healthcare professionals (HCPs) and related partners in line with program and patient activity requirements.
- Convene and Co-ordinate advisory boards, Technical Working Groups and expert panel meetings and roundtables
- Liaison contact between PharmAccess Kenya and PAI Amsterdam medical team.
- Represent the organisation and its senior management whenever required to medico-scientific forums and events.
- Act as the principal delegate to the government on matters affecting medical, clinical and service policy and regulatory provisions
Minimum Qualifications
- Minimum MD (MBChB) qualification holder
- A post-graduate training in medicine or related health services/specialisations will be an added advantage.
Required Skills & Experiences
- At least five years’ post-qualification experience in medical practice or similar roles, with exposure to working in a competitive environment with multiple stakeholders.
- Holder of a valid KMPDCU certification and practice License having fulfilled all requirements.
- Experience working with programs will be a considered advantage.
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