The position

This Feasibility Specialist role has the responsibility for conducting clinical trial feasibility in South Africa affiliate with key investigators at an individual site level on a trial-by-trial basis.
In this role you will be leading and providing input to CDC management on the patient allocation in affiliate in close cooperation with Affiliate Clinical Research Managers and medical team, as well as leading cross-functional review and input on trial portfolio updates.

Your main job tasks will be:

Obtaining internal feedback and data to support feasibility assessments on site/country levels
Building and maintaining sound knowledge of local patient treatment pathways, competitor trials and the clinical research environment for new and established therapy areas
Leading site identification process, ensuring involvement of relevant internal stakeholders
Development of new sites, including required KOL involvement in cooperation with Clinical Medical Manager

Qualifications
We are looking for a candidate who would be fluent in English and has minimum 4 years’ of experience in clinical operations, out of those – 1-2 years with focus on feasibility i.e. most probably you are currently working as a Feasibility Specialist/Analyst/Lead or a Start Up Specialist.
Our ideal candidate also meets the following criteria:

Proven independent decision-making and problem-solving capabilities
Therapeutic knowledge as applicable demonstrated understanding of diseases and treatments
Ability to gather and make sense of information that suggests new possibilities
Ability to communicate with impact and build relationships with internal and external stakeholders at different levels in the organization
Strong ability to drive results