About this role
<p style="text-align:justify"> </p> <p><span style="font-size:12.0px"><span style="font-family:Verdana, Geneva, sans-serif">Work Your Magic with us! </span></span></p> <p> </p> <p><span style="font-size:12.0px"><span style="font-family:Verdana, Geneva, sans-serif">Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. </span></span></p> <p> </p> <p><span style="font-size:12.0px"><span style="font-family:Verdana, Geneva, sans-serif">United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.</span></span></p> <p style="text-align:justify"> </p><p><span style="font-family:verdana, geneva, sans-serif"><strong>Your role:</strong></span></p> <p><span style="font-family:verdana, geneva, sans-serif">As a key member of the drug development team in China R&D, this position will bring critical capacity to support multiple regional clinical trials, build a network of outsourcing resources and strategic plans to capitalize on the growing regulatory and industry development opportunities. Provide scientific, operational, and strategic contributions to the growing China R&D portfolio of activities with a focus on quantitative pharmacology support within the Clinical Measurement Sciences team.</span></p> <p><span style="font-family:verdana, geneva, sans-serif"><strong> </strong></span></p> <p><span style="font-family:verdana, geneva, sans-serif"><strong>Key Responsibilities.</strong></span></p> <ul> <li style="font-family:verdana, geneva, sans-serif"><span style="font-family:verdana, geneva, sans-serif">Drive scientific excellence and contribute expertise to China programs representing quantitative pharmacology in China Program/Project Teams.</span></li> <li style="font-family:verdana, geneva, sans-serif"><span style="font-family:verdana, geneva, sans-serif">Contribute to clinical protocol design, operation planning/logistics. Participate in clinical report and regulatory dossier preparation/review.</span></li> <li style="font-family:verdana, geneva, sans-serif"><span style="font-family:verdana, geneva, sans-serif">Establish and maintain a robust and effective relationship with partner CROs.</span></li> <li style="font-family:verdana, geneva, sans-serif"><span style="font-family:verdana, geneva, sans-serif">Be responsible for quality aspects by supporting in- and external audit/inspection.</span></li> <li style="font-family:verdana, geneva, sans-serif"><span style="font-family:verdana, geneva, sans-serif">Bring integrated strategic thinking and planning cross disciplines with other China R&D line functions.</span></li> </ul> <p><span style="font-family:verdana, geneva, sans-serif">Cooperation Scope.</span></p> <p><span style="font-family:verdana, geneva, sans-serif">Internally</span></p> <p><span style="font-family:verdana, geneva, sans-serif">•Global Quantitative Pharmacology in the CMS functions</span></p> <p><span style="font-family:verdana, geneva, sans-serif">•All departments within R&D China Hub, including but not limited to, </span><span style="font-family:verdana, geneva, sans-serif">Global Clinical Development， </span><span style="font-family:verdana, geneva, sans-serif">Global Regulatory Affairs， </span><span style="font-family:verdana, geneva, sans-serif">Global Development Operation，</span><span style="font-family:verdana, geneva, sans-serif">Global Patient Safety， </span><span style="font-family:verdana, geneva, sans-serif">Clinical Measurement Sciences: Biostatistics, Clinical Biomarker & Diagnostics, APS, and PRWE， </span><span style="font-family:verdana, geneva, sans-serif">External Innovation.</span></p> <p><span style="font-family:verdana, geneva, sans-serif">Externally</span></p> <p><span style="font-family:verdana, geneva, sans-serif">•Contract Research Organizations (CROs)</span></p> <p><span style="font-family:verdana, geneva, sans-serif">•Any external vendor relevant to the project</span></p> <p><span style="font-family:verdana, geneva, sans-serif">•Regional Health Authority (NMPA)</span></p> <p> </p> <p><span style="font-family:verdana, geneva, sans-serif"><strong>Who you are:</strong></span></p> <p><span style="font-family:verdana, geneva, sans-serif">•PhD or Master degree in pharmaceutical, biological or related field with over 10 years of post-graduate experience in the pharmaceutical industry.</span></p> <p><span style="font-family:verdana, geneva, sans-serif">•Excellent verbal and written communication skills in English.</span></p> <p><span style="font-family:verdana, geneva, sans-serif">•Solid, hands-on knowledge of DMPK, toxicology, nonclinical, and clinical pharmacology.</span></p> <p><span style="font-family:verdana, geneva, sans-serif">•Experience working with a CRO or external partner.</span></p> <p><span style="font-family:verdana, geneva, sans-serif">•Good understanding of drug discovery and development process, working experience in GLP and/or GCP.</span></p> <p><span style="font-family:verdana, geneva, sans-serif">•Prior project management, project coordination, and/or contract and budget management experience.</span></p> <p><span style="font-family:verdana, geneva, sans-serif">•Familiar with regulations and guidelines from regional health authorities (e.g. NMPA).</span></p> <p><span style="font-family:verdana, geneva, sans-serif">•Experience working in global industry/academic setting with multi-cultural awareness.</span></p> <p> </p> <p><span style="font-family:verdana, geneva, sans-serif">Location：Beijing / Shanghai, (Beijing is preferred)</span></p><p> </p> <p><span style="font-size:12.0px"><span style="font-family:Verdana, Geneva, sans-serif"><strong>What we offer:</strong> We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!</span></span></p> <p> </p> <p><span style="font-size:12.0px"><span style="font-family:Verdana, Geneva, sans-serif">Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!</span></span></p>