Senior Manager, Clinical Development (Interventional Oncology)

Johnson & Johnson•New Brunswick, PA

6d•Hybrid

About The Position

Johnson & Johnson Innovative Medicine is currently seeking a Senior Manager of Clinical Development in North America and to be located onsite (Hybrid Model) in either Spring House or Horsham, PA; New Brunswick, NJ; or Boston, MA. Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Our Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures. We lead where medicine is going and need innovators with an unwavering commitment to results. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at https://www.jnj.com/innovative-medicine 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. The Senior Manager of Clinical Development will provide scientific, clinical, and operational direction for clinical programs in oncology. Responsibilities include contribution to the design of clinical programs and protocols; conduct and supervision of clinical trials guided by the highest standards of ethics and good clinical practices; development of clinical relationships with both internal and external partners; analysis and reporting of trial results; and interactions with global regulatory agencies.

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.
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 travel approximately 10% of the time is required.

Nice To Haves

Experience in protocol writing and execution is preferred.
Experience in oncology is highly preferred.
Ability to successfully work in a matrixed environment with both internal and external stakeholders including the Oncology community is highly desired.

Responsibilities

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

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.
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 period10 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