Johnson & Johnson

Field Clinical Manager, Interventional Oncology (INTO)

Johnson & Johnson$117K — $201K *
Healthcare
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Biology, Chemistry, Healthcare, or Engineering preferred; equivalent experience acceptable.
  • 7+ years of professional experience in healthcare required.
  • Experience in procedural support within an operating room environment essential.
  • Proven record in teamwork, collaboration, and developing business relationships is necessary.
  • Adaptable self-starter; experience in fast-paced, agile environments preferred.
  • Familiarity with clinical trial execution and ICH GCP guidelines preferred.
  • Technical knowledge of advanced medical technologies like robotics and imaging is a plus.
  • Strong problem-solving skills required for project objectives.
  • Experience with Key Opinion Leader development is advantageous.
  • Willingness to travel extensively (up to 75%) is required.

Responsibilities

  • Act as a liaison between healthcare providers and internal teams to represent trial site needs.
  • Serve as the primary contact for procedural queries at trial sites.
  • Develop relationships with site clinicians to enhance enrollment and collaboration.
  • Advise on training materials to facilitate a skilled trial workforce.
  • Lead on-site or remote training for various teams involved in the trial.
  • Support site feasibility assessments and site initiation visits with clinical operations teams.
  • Maintain relationships with Global Clinical Operations and trial team partners.
  • Gather clinical observations to inform product development activities.
  • Assist in organizing national and regional meetings for investigators.

Benefits

  • Eligible for the company’s consolidated retirement plan and savings plan (401k).
  • Long-term incentive program participation.
  • 120 hours of vacation per calendar year.
  • 40 hours of sick time per calendar year, varying by state of residence.
  • 13 days of holiday pay annually, including floating holidays.
  • Up to 40 hours of personal and family time each year.
  • 480 hours of parental leave within one year of a child's birth or adoption.
  • 240 hours of bereavement leave for immediate family members.
  • 80 hours of caregiver leave in a rolling 52-week period.
  • 32 hours of volunteer leave per year.
Full Job Description
Job Function:
R&D Product Development

Job Sub Function:
Multi-Family R&D Product Development

Job Category:
People Leader

All Job Posting Locations:
Raritan, New Jersey, United States of America

Job Description:

Johnson & Johnson Innovative Medicine is currently searching for the best talent for a Field Clinical Manager, Interventional Oncology in North America. This is a field-based role and while specific cities are listed in the locations section for reference, please note that they are examples only and do not limit your application. We invite candidates from any location within the United States to apply.

The Interventional Oncology (INTO) group, a cross-sector initiative at J&J, brings together the pharmaceutical and medical device expertise with the aim to meaningfully alter the course of cancer and improve survival. 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 critical procedural support at trial sites.

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 best clinical 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


#LI-Remote

Required Skills:

Preferred Skills:

The anticipated base pay range for this position is :
$117,000.00 - $201,250.00

Additional Description for Pay Transparency:
Subject to the terms of their respective plans, employees are eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).

This position is eligible to participate in the Company's long-term incentive program.

Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:
Vacation -120 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado -48 hours per calendar year; for employees who reside in the State of Washington -56 hours per calendar year
Holiday pay, including Floating Holidays -13 days per calendar year
Work, Personal and Family Time - up to 40 hours per calendar year
Parental Leave - 480 hours within one year of the birth/adoption/foster care of a child
Bereavement Leave - 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
Caregiver Leave - 80 hours in a 52-week rolling period 10 days
Volunteer Leave - 32 hours per calendar year
Military Spouse Time-Off - 80 hours per calendar year

For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits

About Johnson & Johnson

Scio Diamond creates single-crystal Type IIa diamonds for the jewelry market and for industrial applications. It employs a patent-protected chemical vapor deposition (CVD) process in a precisely controlled laboratory setting to produce diamonds. It was founded in 2009 and is headquartered in Greenville, South Carolina.

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Learn more about Johnson & Johnson
Size
141,700 employees
Market Cap
$462.7 billion
Industry
Net Income
$14.7 billion
Founded
1886
5 Year Trend
+5.5%
Revenue
$82.5 billion
NASDAQ

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