Site relationship management role to ensure sustainable trial execution at Site. Performs on-site and remote monitoring activities related to initiation, conduct and timely completion of Phase I-IV GDD trials within the country in adherence with monitoring procedures and processes in accordance with ICH/GCP, local regulations and SOPs. Proactive site performance management (recruitment & quality) and early identification of real site needs and issues as the single best point of contact (internally & externally) for all sites. (from issue management to risk identification).

Key responsibilities:

•Frontline liaison between Novartis and sites to ensure successful collaboration, meeting Novartis expectation on milestone and deliverables with true ownership mindset

•Manages assigned study sites, conducting phase I-IV protocols according to the Monitoring Plan and Novartis procedures

•Performs Site Initiation Visit, ensures site personnel is fully trained on all trial related aspects. Performs continuous training for amendments and new site personnel as required. Re-trains site personnel as appropriate

•Conducts continuous site monitoring activities (onsite and remote). Implements site management activities to ensure compliance with protocol, ICH/GCP, global and local regulation including Health Authorities, IRB/EC, data privacy requirements, global and local processes as applicable. Documentation according to GDP and Novartis standards.

•Identifies deficiencies in site processes and monitor site processes performed outside the site, works in close collaboration with site on risks mitigation and process improvements

•Promotes a compliance culture advocating adherence to highest standards and ethical integrity, ensuring human subject protection and reliability of trial results at all times

•Identify deficiencies in site process, work in close collaboration with site on risk mitigation

•Establish a strong partnership and true collaboration with the site, to increase patient density and decrease issues at site.

•Early engagement with site on patient inventory and patient flow in advance of SIV in close collaboration with global and local study team

•Performs Site Closeout activities per SOPs and applicable regulations to ensure that site is aware of any follow up activity and archiving requirements

•Attends onboarding-, disease indication and project specific training and general CRA training as required

•Proactively collaborates with the SSO Clinical Project Manager (CPM) and CRA Manager as well as MSL, CRMA and medical advisor to ensure optimal recruitment, site development and data quality

•Ensures that relevant site insights are shared with internal stakeholders such as site partnership manager, medical advisor, MSL and CRMA etc. to improve one Novartis approach to sites

•Participates in audit organization and inspection readiness activities for monitoring and site related activities as required and ensures implementation of corrective actions within specified timelines

•Collaborates with internal stakeholders and site personnel to manage data query resolution process and to ensure timely and accurate data entry

•Ensures the site Investigator Folder is up to date. Responsible for collecting essential documents from site and accountable to keep sTMF(s) up to date

Essential requirements：

•2+ years pharmaceutical industry experience or other relevant experience

•Central/in-house monitoring or field monitoring experience is desirable

•Decision capability

•Excellent time management and organization capabilities, including ability to prioritize and multi-task

•Risk based mindset (from issue management to risk identification) supported by Novartis systems

•Early adopter and open mindset across borders to support one study approach

•Good knowledge of drug development process specifically clinical trial/research

•Clinical and therapeutic knowledge

•Knowledge of international standards (GCP/ICH, FDA, EMA)

•Understanding the purpose of the CRA (Patient Safety

Data Integrity

PI oversight

GCP/ICH & Protocol Compliance)

•Ability to travel domestically (and possibly internationally) as needed to study sites and for training and meetings.

•A minimum of 50% overnight travel may be required

Desirable requirements：

•Fast change adaptability to best partner & influencing with sites on fast changing landscape

•Trust and rapport building is a very important skill needed

•Good communication skills, ability to influence others & Relationship management

•Excellent communicator and presenter (oral and written)

•Ability to manage sites independently

Proven ability to work independently with minimal supervision

•Good analytical thinking

•Ability to anticipate potential issues and take appropriate actions with or without supervision

•Digital & tech capabilities, including computer skills (Microsoft platforms)

为什么选择诺华：帮助患者及家属不仅需要创新科学，还需要一支包括你我他在内的充满智慧与激情的团队，大家相互协作、支持与激励。共同实现突破，改变患者的生活。一起共创更好的未来，你准备好了吗？

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Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together?

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