Field Clinical Manager, Interventional Oncology
At Johnson & Johnson, we are committed to redefining healthcare: connecting the best of health and care for every provider, for every patient, for everyone. We are leading where medicine is going. With a focus on treating with pinpoint precision in the hardest-to-reach parts of the body, we confidently address the most complex diseases of our time and unlock the potential medicines and therapeutic procedures of tomorrow. We bring together individuals who demonstrate a strong drive for scientific exploration and actively contribute to advancing global health.
One of our key initiatives is Interventional Oncology, a cross-sector effort charged by the Executive Committee of Johnson & Johnson with altering the course of cancer. We conduct sophisticated clinical trials that involve the development of novel procedures and unique routes of administration for investigational cancer therapies. To ensure the success of these trials, we are seeking an exceptional Field Clinical Manager to provide crucial procedural support at trial sites.
Responsibilities
As a Field Clinical Manager, you will play a pivotal role in bridging the gap between investigators, and multiple functions within our global and regional study teams. Your primary responsibility will be to ensure that clinical trial procedures are performed in compliance with the protocols developed by our cross-sector Development Teams. Your key responsibilities will include:
- Acting as a liaison between external healthcare providers (e.g., surgeons, interventionalists, and oncologists,) and internal teams, representing procedural needs of clinical trial sites
- Serving as the point of contact responsible for answering procedure-related questions at the site, or passing them on to the appropriate medical study team members
- Supporting the translation of Clinical Engineering workflows into tactical requirements for specific trial sites
- Leading on-site or remote training for pharmacy, OR suite, and administration teams
- Supporting site feasibility assessments, site qualification visits (SQVs), and site initiation visits (SIVs), in partnership with clinical operations, as we build a global clinical trial network
- Developing clinical observations and insights to guide product development activities
- Developing robust relationships with site clinicians and teams to enhance the site experience, support enrollment, foster collaboration, and optimize procedural workflow
- Attending and assisting with organizing national, regional, and global meetings, including investigator meetings
Working Location: Shanghai or Beijing
