Medical Enabler Ophthalmology – Pharmaceutical
Please note that preference will be given to BBBEE candidates due to BEE requirements.
Location: Midrand
Position Overview:
A leading multinational pharmaceutical manufacturer is looking to appoint a Medical Enabler over the Ophthalmology therapeutic / disease area.
The Medical Enabler is a Ophthalmology therapeutic / disease area expert and supports the Primary Point of Contact (PPOC) in the Ophthalmology area. The role ensures both medical/scientific expertise independent from promotional objectives in all their decisions.
The Medical Enabler works with the PPOC to gain a deep understanding of the relevant patient journey and area ecosystem needs. They collaborate and derive actionable insights that inform the Therapeutic Area strategy. They proactively enable co-creation and delivery of national-level activities that deliver tangible value to the medical community and transform clinical practice.
The Medical enabler develops broad medical and scientific expertise, often across multiple molecules or indications within a given Therapeutic Area and drives evidence generation and scientific exchange activities. This is a network role that fosters and enhances collaboration and coordination across the formal and informal network - in country, across countries or as seen relevant to serve patients across the enterprise. The role is anticipated to spend most of its time serving the local ecosystems.
They remain focused on supporting high-value and high-impact activities that either directly, or indirectly, touch the patient journey.
The Medical Enabler is a fluid member of one or more Therapeutic Area aligned working teams according to evolving needs. Together with the PPOCs they maintain strong relationships with TAEs and partner with them on national-level initiatives as appropriate.
Essential Experience, Qualifications and Skills Required
Minimum Requirements:
- Medical degree, PhD/PharmD/Masters in Science (MSc) degrees required
- 3-5 Years commercial Ophthalmology (surgical experience required) in a multinational environment.
- Established knowledge base/ skill set in: Data generation (clinical trials; IIS, RWE programs)
- Understanding of clinical trial design, interpretation, and biostatistics
If you meet all the requirements specified above, and interested to further the process, kindly send your detailed CV to Patricia at
