The primary responsibility of the CRP is to provide medical expertise to clinical strategic planning and execution, all aspects of the local business, and to ultimately enhance the customers' experience.
Take core role in collaborating with the global teams (or leading if assigned for China lead multi-country study) in the clinical development strategy, study planning, designing, startup and conduct of phase I-IV clinical trials, analysis and reporting of China data (or study data), as well as non-clinical trial solutions/activities that are conducted in China.
Take core role and collaborate with registration affairs staff in communicating with health authorities during clinical trial permission (CTP) and new drug application (NDA) process.
Take a leadership role in defining the patient Journey, evidence gap, and developing integrated evidence generation plan and medical strategy. Become patient advocate, as well as a medical expert.
Contribute actively on an ongoing basis to the strategic planning for currently marketed brands and support brand commercialization activities during the development of the local business plan.
Contribute as a scientific and medical expert to activities and deliverables of the PRA organization, in particular giving clinical input and insight to develop payer partnership programs and defend the product value, supporting negotiation strategy development and dossier preparation.
Strategically lead and contribute on planning and execution of medical meetings (scientific exchange meetings, advisory board meetings, and/or other meetings with health care professionals), real world study, data analysis and publication development (abstracts, posters, manuscripts) while ensuring compliance.
Establish and maintain appropriate collaborations and relationships with external scientific experts, thought leaders, and the general medical community.
