Assume overall direct responsibility for the deliverable of the Medical Market Shaping output, manage all milestones, timelines, and any emerging interdependencies
Lead the implementation of the Medical Market Shaping working
Location:
Parktown - Johannesburg
Key performance areas:
Provide overall project leadership of market surveillance
Develop market shaping strategy and detailed annual work plans
Facilitate and lead deal design
Identification and design of market-shaping interventions
Oversee the development of technical content needed to engage with all external stakeholders
Lead and coordinate implementation of the market-shaping output
Develop and maintain a strong relationship with Unitaid (donor) as relates to the market-shaping output work
Manage the contractual relationship with CHAI and ensure that they, as sub-grantee meet all their key technical deliverables
Work closely with CHAI and oversee the implementation and monitoring of defined supply-side interventions
Manage the contractual relationship with various drug manufacturers as relates to incentives
Manage the day-to-day relationships with all stakeholders, in particular with CHAI, and maintain technical oversight over their deliverables and all other stakeholder inputs
Ensure comprehensive and timely reporting to Unitaid
Contribute to the strategic direction to the project
Develop and effectively manage relationships with relevant Wits RHI structures
Manage day-to-day operations and coordination of the market-shaping output
Ensure project deliverables are on track to deliver high quality, timeous, successful project outcomes
Oversee coordination between the two output streams: (1) Supplier Engagement/Contract Management; (2) Drug Development & Regulatory Processes
Ensure the market shaping work (output 4) dovetails with other Unitaid-funded work, particularly Project PrEP (output 1, 2, and 3)
Oversee the management of the broader market-shaping output team - 6 team members in total
Manage the market shaping budget - e.g., oversee and approve such aspects such as payments to CHAI and incentives to drug manufacturers
Report monthly on key achievements, challenges, and any anecdotal success stories
Support financial management and control as related to the above Human Resources and other activities
Plan, convene, and produce reports for monthly one-on-one meetings with supervised staff to monitor performance and support
Attend to all staffing requirements and administration
Oversee the duties of subordinates to ensure optimal staff utilization and maintenance of sound labor relations
Plan, organize and lead staff performance assessments
Identify substandard performance by team members and plan and implement necessary corrective action
Coach and train subordinates and team members to ensure the acquisition of knowledge and skills required by the organization
Lead the promotion of harmony, teamwork, and sharing of information
Provide day-to-day support to all project staff
Take ownership and accountability for tasks and demonstrate effective self-management
Follow through to ensure that quality and productivity standards of own work are consistently and accurately maintained
Maintain a positive attitude and respond openly to feedback
Take ownership of driving your own career development by participating in ongoing training and development activities such as forums, conferences, policy-setting workshops, etc.
Required minimum education and training:
A Graduate-level Degree with significant experience in product development, commercialization and regulatory affairs, including conceptualization, design, and execution of market-shaping opportunities
Required minimum work experience:
Minimum 10 years of work experience, with a focus on product development commercialization and regulatory affairs, including conceptualization, design, and execution of market-shaping opportunities
Experience leading strategy development to overcome key barriers and issues related to product development and commercialization, filing, approval, introduction, and adoption
Extensive experience developing and managing senior-most relationships with manufacturers, procurement, and other partners, Stringent Regulatory Authority (SRAs), National Drug Regulatory Authorities (NDRA), Ministries of Health, and other key stakeholders, including innovator and generic product manufacturers
Experience leading capacitation of new/junior team members with more limited experience in product development and commercialization and regulatory affairs
Ability to collaborate remotely with team members spread across geographies
Desirable additional education, work experience, and personal abilities:
Good interpersonal skills and ability to navigate complicated situations, excellent levels of written and verbal English communication skills, ability to communicate in other SA languages, preferably area-appropriate
Demands of the job:
Travel will be required within and outside of South Africa
Work can be highly demanding and pressurized, and requires flexibility, management, training, and leadership experience
TO APPLY:
Only if you do meet the minimum job requirements and experience as mentioned above, you may submit a detailed updated CV.
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