This highly visible position is for Clinical Pathologist- Director, Medical Affairs for implementation of quality standards, assuring regulatory compliance and clinical consultation for the laboratory component of Pharmaceutical Trials.
In this role, the selected candidate will conduct peer to peer scientific discussions and maintain a reliable presence with those thought leaders to ensure they have a medical contact within the company.
In this role, the selected candidate will leverage professional network to cultivate new clients and new business opportunities; provide expert consultation and supports the due diligence research of select compounds and/or companies.
As a Safety Medical Director, you will be responsible for managing safety input into global or regional therapeutic or research projects or acting as an expert involved in the design, conduct, monitoring, data interpretation and reporting of safety data across disease areas and trial programme.
In this role, you will be responsible for managing safety input into global or regional therapeutic or research projects involved in the design, conduct and reporting of safety data across disease areas and trial programme
In this role, you will play an integral role in the planning and participation of national and regional medical advisory boards. Play an integral role in the planning and providing of training for external medical/scientific speakers.
In this role, you will be responsible for
generate diagnostics related insight to shape US input into the development and regulatory approach for the brand and product during development, and LCM brand strategy and tactics.
In this role, the selected candidate will lead and foster the development of Inovalon process improvement, quality assurance, productivity & efficiency initiatives for Medical Record Review Operations and Medical Record Review Quality Operations.