* Job title Field Clinical Manager, Interventional Oncology
* Function R&D Operations
* Sub function Clinical Trial Project Management
* Category Manager, Clinical Trial Project Management (P7)
* Location North Ryde / Singapore / Mongkok / Eight Mile Plains / Norwood / Taipei City / Notting Hill, / Australia / Singapore / Hong Kong / Taiwan
* Date posted Dec
* Requisition number R-
* Work pattern Field-based
Description
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at
Job Function
R&D Operations
Job Sub Function
Clinical Trial Project Management
Job Category
Professional
All Job Posting Locations
Eight Mile Plains, Queensland, Australia, Mongkok, Kowloon, Hong Kong, North Ryde, New South Wales, Australia, Norwood, South Australia, Australia, Notting Hill, Victoria, Australia, Singapore, Singapore, Taipei City, Taiwan
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, Hong Kong, Australia, or Singapore. Please indicate which location(s) you are applying for.
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
* 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, local languages are plus.
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
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