- Act as a medical resource to the company as a whole and particularly to the clinical research department (protocol, CSR writing/ review, adverse events, discussions with investigators, internal meetings).
- To have responsibility for nominated therapeutic areas and assume overall management of the clinical trials within these areas
- To be recognized as a company expert in the nominated therapeutic areas and provide input into in product development teams.
- Represent the company via presentations to groups of experts, societies, regulatory bodies and at international meetings.
- Write clinical development plans, develop budgets, & provide drug development inputs
- Establish ongoing liaison with key opinion leaders and to ensure that significant developments in the field are identified and monitored.
- Provide medical expertise in the review of adverse experiences and discuss patient management issues with investigators.
- Attend and contribute to interdisciplinary team meetings relating to clinical investigational drug trials
- Effectively collaborate with colleagues in related project team departments such as Regulatory, Quality Assurance, anufacturing, Bioanalytical , PK/PD, Discovery, and Marketing
Apply now
Posts
