Global Clinical Lead- Hematology

Main Responsibilities and Accountabilities:  

GCL Line Manager responsibilities include: 

• Providing strategic and tactical medical leadership and guidance for clinical development activities in for 5-8 GCPLs 

• Works with other GCLs and head of clinical to ensure adequate resourcing across the portfolio 

• Manages team of clinical drug developers, acts as a mentor to physician group in guide clinical development expertise in general and in specific areas of therapeutic knowledge 

GCL TALT CD Representative responsibilities include:  

• Defining the global clinical development strategy for all projects in TA 

• Contributing to BD strategy & due diligence for TA & identifies and evaluates NPO’s 

• Ensuring high quality clinical & scientific content is provided into Regulatory submissions & ensures defense and negotiation with Regulatory agencies 

• Preparing for stage-gate evaluations and benefit –risk evaluations and assessments 

• Overseeing and supports the clinical development activity of assigned Clinical Development reports and works in a matrix with CDT leads and Global Project Leaders to ensure optimal clinical strategy, CDP and protocol design to support optimal Project strategy 

GCL Other Responsibilities include: 

• Be an active member of the Clinical Development Leadership Team, improving the overall quality of the group and its deliverables 

• Ensuring that the patient and physician voice is at the forefront in strategy development 

• Building networks with external experts 

• Driving excellence in clinical development execution 

• Partnering with TA core, extended core & functional partners to ensure scientific & medically robust clinical dev & med affairs activities 

• Enhancing the reputation of the Company through thought leadership, KOL interactions in fundamental issues affecting the TA 

• Representing the Co & TA externally with KOL, Health Technology and external authorities at key forums 

• Ensuring effective presentations at Scientific and Technical Review Committee 

• Representing the clinical function on the TALT, responsible for input into TALT strategy, oversee the quality of clinical plans in the CVR TA. 

Position Qualifications and Experience Requirements:

• MD, Board Certified (or non-USA equivalent) with relevant sub-specialty highly preferred- if not Board Certified in relevant Subspecialty, then experience in that TA is a must.