Johnson & Johnson

Senior Manager, Clinical Development – Interventional Oncology

Johnson & Johnson

full-time

Posted on:

Location Type: Hybrid

Location: Spring House • Massachusetts, New Jersey, Pennsylvania • 🇺🇸 United States

Visit company website
AI Apply
Apply

Salary

💰 $137,000 - $235,750 per year

Job Level

Senior

About the role

  • Perform medical monitoring of clinical trial data
  • Contribute to design and approval of clinical trials
  • Support preparation and implementation of clinical trial protocols
  • Implement and maintain high standards of research conduct
  • Participate in the development & execution of study operational plans
  • Collaborate with individuals and groups within the organization to share information, transfer technology, and further scientific partnership
  • Collaborate with external partners including vendors (e.g. CRO, central labs) and investigators
  • Work cross-sector in pharmaceutical and/or medical device spaces

Requirements

  • A Bachelor’s degree in a scientific or related discipline is required.
  • An advanced degree in a scientific discipline (e.g. Master’s degree in scientific field or PhD or PharmD) is preferred.
  • Six to nine years or more of clinical/biomedical research experience in or outside of the industry setting is required.
  • Experience in protocol writing and execution is preferred.
  • Experience in oncology is highly preferred.
  • Demonstrated ability to present scientific content to diverse audiences is required.
  • Learning agility and ability to work across multiple sectors (Pharmaceutical, Medical Device, and or Consumer) is required.
  • Ability to successfully work in a matrixed environment with both internal and external stakeholders including the Oncology community is highly desired.
  • Ability to travel approximately 10% of the time is required.
Benefits
  • 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.
  • 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

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard skills
clinical trial data monitoringclinical trial designclinical trial protocol preparationresearch conduct standardsstudy operational plans developmentprotocol writingoncology researchbiomedical research
Soft skills
collaborationcommunicationpresentation skillslearning agilitymatrixed environment adaptability
Certifications
Bachelor’s degreeMaster’s degreePhDPharmD