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Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
Professional
All Job Posting Locations:
Beijing, China, Shanghai, China
Job Description:
Johnson & Johnson is recruiting for a Field Clinical Manager, Interventional Oncology, to be based in one of our major locations:
Mainland China, Taiwan, Australia, or Singapore. Please indicate which location(s) you are applying for.
- Mainland China: Apply through R-048891 – Field Clinical Manager, Interventional Oncology
- Taiwan, Australia, or Singapore: Apply through R-050124 – Field Clinical Manager, Interventional Oncology
Responsibilities:
As a Field Clinical Manager, you will play a pivotal role in bridging the gap between investigators, our local teams, and multiple functions within our global 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 (surgeons and interventionalists) and internal teams, representing the 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
Developing robust relationships with site clinicians and teams to enhance the site experience, support enrollment, foster collaboration, and optimize procedural workflow
Advising on training materials through collaboration with internal team members to enable a skilled and proficient trial workforce
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
Establishing and maintaining relationships with internal Global Clinical Operations and trial team partners
Developing clinical observations and insights to guide product development activities
Attending and assisting with organizing national, regional, and global meetings, including investigator meetings
Proactively collaborating with the Interventional Oncology key opinion leaders and consulting network to advise trial sites best practices
Collaborate with INTO KOL and consulting network to advise trial sites on clinical best practices
Qualifications and Requirements:
To be successful in this role, you should possess the following qualifications and skills:
Equivalent experience is acceptable in lieu of a Bachelor's degree. However, a degree in the fields of Biology, Chemistry, Healthcare and/or Engineering is strongly preferred
Seven or more years of professional experience in the healthcare industry is required
Experience as an industry representative or procedural support role in an operating room environment is required
A proven track record of teamwork, collaboration, inclusion, and developing strong business relationships with internal teams and outside partners is required
An adaptable self-starter mentality is required; experience and comfortability navigating an agile start-up type environment is preferred
Experience in clinical trial execution and familiarity with ICH Guidelines for Good Clinical Practice (GCP) is preferred
Technical experience with sophisticated medical technology used in surgical procedures such as robotics and medical imaging is preferred
Strong problem-solving skills for developing creative solutions and meeting project objectives is required
Experience with Key Opinion Leader (KOL) development and management is preferred
Willingness and ability to travel domestically and/or internationally up to 75% of the time is required
Consistently monitors and adheres to key performance indicators (KPIs), using goals and insights to meet or exceed critical metrics and continuously improve performance
Fluency in English language is required
Required Skills:
Preferred Skills:
Analytical Reasoning, Budgeting, Clinical Trial Management Systems (CTMS), Clinical Trials, Compliance Management, Contract Management, Execution Focus, Fact-Based Decision Making, Laboratory Operations, Mentorship, Process Improvements, Project Integration Management, Research and Development, Research Ethics, Standard Operating Procedure (SOP), Technical Credibility
