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
-Accountable/Responsible to interpret requirements to translate and document them into project / TA level technical specifications. Provision clinical project / TA level data to business consumers. Facilitate requirements gathering from consumers and develop global solutions to meet immediate and long-term needs of the business. Monitor and maintain ongoing project / TA level operations of clinical data environments, and respond to project / TA issues.

-Leads and oversees all CDE tasks performed by an external partner. Oversees CRO capacities/budget for outsourced trial/project tasks.

-Develop/test different ways to constantly improve data reliability, integrity and quality. Ensures real-time inspection readiness of all data collection, data review/data delivery (DBL) deliverables for a trial/project and participates in regulatory agency and BI internal audits as necessary.

-Collaborate with / Influence members of the development team within BDS and with neighboring colleagues at company on the project/product goals. Contributes to cross-functional- and team-based thinking.

Qualifications
- Bachelor’s degree or Master’s degree (e.g. MBA, MSc) in Life Sciences, Computer Science, Software/Computer Engineering, or similar preferred.

- In-depth knowledge and experience with the use of Data Collection Tools (EDC systems), Data Review Tools, and/or Data Standardization methods, requirements

- Thorough knowledge/experience in design of clinical trials, basic medical terminology and on processing clinical trial information

- Excellent organizational skills, problem solving abilities, negotiation skills, time management skills and initiative required.

- Strong communication skills: Confident and persuasive communicator to ensure that the message is clear and well understood.

- Ability to work collaboratively on multi-disciplinary project teams and proactively manage relationships with external vendors required.

- Mindful of local, global, internal and external cultures to ensure that messages are received positively and effectively.

- Ability to lead and facilitate meetings required.

- Ability to develop and deliver (technical) training required.

Language skills:English: fluent (Read/Write/Speak)