Key responsibilities <ul style="margin-bottom:0.0cm;margin-top:0.0px"> <li style="margin:0.0cm 0.0cm 2.0pt 0.0px;line-height:14.0pt;Apis For Office', sans-serif;text-indent:4.9333px">Clinical Medical Managers deliver industry-leading clinical trial excellence and early therapy area development, with high-quality scientific insights and engagement, trusted partnerships, and innovation. They work in close partnership with Clinical Operations and Medical & Scientific Affairs to connect product development and world-class clinical trial execution with early therapy area development and successful product launches.</li> </ul> Main job tasks 1）Deliver industry-leading clinical trial excellence with scientific insights and external engagement <ul style="margin-top:0.0cm;margin-bottom:0.0cm"> <li style="margin:0.0cm 0.0cm 0.0cm 10.0px;line-height:normal;Apis For Office', sans-serif;text-indent:10.0px">Partner with Clinical Operations Therapy Area Leads and Trial Managers on scientific and medical aspects of early trial planning, start up, recruitment and retention</li> <li style="margin:0.0cm 0.0cm 0.0cm 10.0px;line-height:normal;Apis For Office', sans-serif;text-indent:10.0px">Gather, analyse, communicate and implement actionable insights throughout the lifecycle of assigned clinical trials</li> <li style="margin:0.0cm 0.0cm 0.0cm 10.0px;line-height:normal;Apis For Office', sans-serif;text-indent:10.0px">Provide scientific inputs to trial portfolio review, country allocation and site feasibility processes</li> <li style="margin:0.0cm 0.0cm 0.0cm 10.0px;line-height:normal;Apis For Office', sans-serif;text-indent:10.0px">Lead ‘National Leader’ selection for relevant trials, and secure consideration for investigators who are important key opinion leaders during product launch for inclusion in the trials</li> <li style="margin:0.0cm 0.0cm 0.0cm 10.0px;line-height:normal;Apis For Office', sans-serif;text-indent:10.0px">Secure actionable scientific insights into protocol outline and trial execution to enhance outcomes</li> <li style="margin:0.0cm 0.0cm 0.0cm 10.0px;line-height:normal;Apis For Office', sans-serif;text-indent:10.0px">Contribute to site selection criteria, and assess medical capabilities as well as scientific training needs at sites</li> <li style="margin:0.0cm 0.0cm 0.0cm 10.0px;line-height:normal;Apis For Office', sans-serif;text-indent:10.0px">Engage relevant key opinion leaders who are investigators to optimise trial methodologies, mitigate recruitment and retention challenges, and build long-term relationships</li> <li style="margin:0.0cm 0.0cm 0.0cm 10.0px;line-height:normal;Apis For Office', sans-serif;text-indent:10.0px">Secure investigators and relevant site staff are well versed before FPFV with scientific aspects of the product, protocol, and measures to recruit and retain patients</li> <li style="margin:0.0cm 0.0cm 0.0cm 10.0px;line-height:normal;Apis For Office', sans-serif;text-indent:10.0px">Be the local subject matter expert on the product and protocol in relevant trials to discuss early clinical data with external experts during feasibility and to quickly resolve medical queries from site staff during the trial</li> <li style="margin:0.0cm 0.0cm 0.0cm 10.0px;line-height:normal;Apis For Office', sans-serif;text-indent:10.0px">Continuously monitor trial performance with Therapy Area Leads and Trial Managers and take proactive measures to address scientific issues (during retention Clinical Operations lead retention efforts and involve CMMs only if needed for scientific aspects)</li> </ul> 2）Secure early inputs to product development, incorporating voice of patients and clinicians <ul style="margin-top:0.0cm;margin-bottom:0.0cm"> <li style="margin:0.0cm 0.0cm 0.0cm 10.0px;line-height:normal;Apis For Office', sans-serif;text-indent:10.0px">Provide early medical and scientific input into product development, incorporating the perspectives of clinicians and patients</li> <li style="margin:0.0cm 0.0cm 0.0cm 10.0px;line-height:normal;Apis For Office', sans-serif;text-indent:10.0px">Identify and address potential challenges in product development through proactive scientific insights and stakeholder engagement.</li> </ul> 3）Establish a strong presence in new and current therapy areas <ul style="margin-top:0.0cm;margin-bottom:0.0cm"> <li style="margin:0.0cm 0.0cm 0.0cm 10.0px;line-height:normal;Apis For Office', sans-serif;text-indent:10.0px">Effectively communicate Novo Nordisk pipeline and scientific narrative to external stakeholders, especially those new to Novo Nordisk</li> <li style="margin:0.0cm 0.0cm 0.0cm 10.0px;line-height:normal;Apis For Office', sans-serif;text-indent:10.0px">Establish strong relationship with key stakeholders in new and current therapy areas through scientific engagement in trials</li> <li style="margin:0.0cm 0.0cm 0.0cm 10.0px;line-height:normal;Apis For Office', sans-serif;text-indent:10.0px">Secure mapping and updating of clinical care pathways for effective recruitment (including referrals) and retention in trials.</li> </ul> 4）Build organizational readiness <ul style="margin-top:0.0cm;margin-bottom:0.0cm"> <li style="margin:0.0cm 0.0cm 0.0cm 10.0px;line-height:normal;Apis For Office', sans-serif;text-indent:10.0px">In collaboration with Therapy Area Leads, co-design and deploy scientific knowledge building for Clinical Operations teammates on therapy area, product and protocol</li> <li style="margin:0.0cm 0.0cm 0.0cm 10.0px;line-height:normal;Apis For Office', sans-serif;text-indent:10.0px">Continuously exchange insights and introduce Medical Affairs colleagues to KOLs in new therapy areas, especially during pre-launch</li> </ul> 5）Medical support to regulatory interaction <ul style="margin-top:0.0cm;margin-bottom:0.0cm"> <li style="margin:0.0cm 0.0cm 0.0cm 10.0px;line-height:normal;Apis For Office', sans-serif;text-indent:10.0px">Medical input for clinical development strategy</li> <li style="margin:0.0cm 0.0cm 0.0cm 10.0px;line-height:normal;Apis For Office', sans-serif;text-indent:10.0px">Medical review and input for regulatory interactions and submissions</li> </ul> Other areas of responsibility <ul style="margin-bottom:0.0cm;margin-top:0.0px"> <li style="margin:0.0cm 0.0cm 0.0cm 0.0px;line-height:14.0pt;Apis For Office', sans-serif;text-indent:4.9333px">Be presenter at scientific conferences for oral presentation/poster based on NN sponsored trials</li> <li style="margin:0.0cm 0.0cm 0.0cm 0.0px;line-height:14.0pt;Apis For Office', sans-serif;text-indent:4.9333px">Be flexible to support projects as needed</li> </ul> Qualifications <ul style="margin-bottom:0.0cm;margin-top:0.0px"> <li style="margin:0.0cm 0.0cm 0.0cm 0.0px;line-height:14.0pt;Apis For Office', sans-serif;text-indent:4.9333px">MD, PhD, MSc, MPharm or equivalent in healthcare with strong background in clinical practice or research background</li> <li style="margin:0.0cm 0.0cm 0.0cm 0.0px;line-height:14.0pt;Apis For Office', sans-serif;text-indent:4.9333px">3+ years’ experience in clinical or medical roles in the pharmaceutical industry</li> <li style="margin:0.0cm 0.0cm 0.0cm 0.0px;line-height:14.0pt;Apis For Office', sans-serif;text-indent:4.9333px">Strong understanding of pharmaceutical drug development and value chain</li> <li style="margin:0.0cm 0.0cm 0.0cm 0.0px;line-height:14.0pt;Apis For Office', sans-serif;text-indent:4.9333px">Strong knowledge of ICH-GCP guidelines, regulatory requirements, and clinical trial methodology</li> <li style="margin:0.0cm 0.0cm 0.0cm 0.0px;line-height:14.0pt;Apis For Office', sans-serif;text-indent:4.9333px">An enterprise mindset demonstrating business understanding, prioritizing the organisation's overall success over own interests, and promoting cross-functional collaboration</li> <li style="margin:0.0cm 0.0cm 0.0cm 0.0px;line-height:14.0pt;Apis For Office', sans-serif;text-indent:4.9333px">Strong business acumen and understanding of business operations, financial drivers, and market dynamics</li> <li style="margin:0.0cm 0.0cm 0.0cm 0.0px;line-height:14.0pt;Apis For Office', sans-serif;text-indent:4.9333px">Excellent written and verbal communication, presentation skills and stakeholder management skills</li> <li style="margin:0.0cm 0.0cm 0.0cm 0.0px;line-height:14.0pt;Apis For Office', sans-serif;text-indent:4.9333px">Excellent ability to build and maintain strong relationships with internal and external stakeholders</li> <li style="margin:0.0cm 0.0cm 0.0cm 0.0px;line-height:14.0pt;Apis For Office', sans-serif;text-indent:4.9333px">Ability to creatively solve complex problems and drive the development of practical solutions.</li> <li style="margin:0.0cm 0.0cm 0.0cm 0.0px;line-height:14.0pt;Apis For Office', sans-serif;text-indent:4.9333px">Ability to innovate, identify opportunities for continuous improvement, and embrace change</li> <li style="margin:0.0cm 0.0cm 2.0pt 0.0px;line-height:14.0pt;Apis For Office', sans-serif;text-indent:4.9333px">Willingness to leverage technology such as AI tools and adopt a data-driven approach in all aspects of work</li> </ul>We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.

Clinical Medical Manager (Beijing, Beijing, CN) @ novonord

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