Job Description

About Human Pharmaceutical Business

With global presence, Boehringer Ingelheim has industry-leading expertise in medicine research and development. We are constantly developing the next generation of medical breakthroughs and successfully delivering innovations to meet the medical needs of the patients we serve in the following key areas of interest: cardiovascular, respiratory, metabolic diseases, immunology, oncology and central nervous system. In the future, we will accelerate the launch of more than 10 innovative medicines to meet the demand of Chinese patients.

Responsibilities
- Adheres to trial planning and commitment as per MedEx target KPIs. Core documents filed in Trial Master File as per planned timelines. Ensures timely update of trial management systems.

-Regular communication maintained with local trial team, internal and external partners.

-Implementation and incorporation of patient centric initiatives to optimize trial delivery and bring value to patients. Engagement plans in place, including recruitment and contingency planning.

-Regular reporting of trial budget and mitigation of significant budget deviations.

-Timely responses to authority and ethics requests.

-Vendor services proceed without interruption, and all issues are promptly escalated and documented.

-Trial target meets commitments.

-Effective teamwork & leadership, goal delivery and efficient delivery of operational aspects aligned to the One Medicine visions (including goals, risk, mitigation).

Qualifications
-8+ years of relevant experience in the clinical research field with 3-5 years of experience in clinical project management.

-Scientific and therapeutic knowledge and operational expertise across all aspects of clinical trial planning and execution.

-Strong communication skills in complex cross-functional matrix structures of the trial and extended team. Active listening skills and cultural awareness.

-Proficient in the English